Anti-TRAP alpha/TRAPA/SSR1 Antibody Picoband®

Western blot analysis of TRAP Alpha/TRAPA/SSR1 using anti-TRAP Alpha/TRAPA/SSR1 antibody (A06993-1).
Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human A431 whole cell lysates,
Lane 2: human HL-60 whole cell lysates,
Lane 3: human T-47D whole cell lysates,
Lane 4: human HepG2 whole cell lysates,
Lane 5: monkey COS-7 whole cell lysates,
Lane 6: human HEK293 whole cell lysates,
Lane 7: human K562 whole cell lysates,
Lane 8: human U937 whole cell lysates,
Lane 9: rat liver tissue lysates,
Lane 10: rat stomach tissue lysates,
Lane 11: rat PC-12 whole cell lysates,
Lane 12: mouse liver tissue lysates,
Lane 13: mouse stomach tissue lysates.
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRAP Alpha/TRAPA/SSR1 antigen affinity purified polyclonal antibody (Catalog # A06993-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TRAP Alpha/TRAPA/SSR1 at approximately 36 kDa. The expected band size for TRAP Alpha/TRAPA/SSR1 is at 32 kDa.

IHC analysis of TRAP Alpha/TRAPA/SSR1 using anti-TRAP Alpha/TRAPA/SSR1 antibody (A06993-1).
TRAP Alpha/TRAPA/SSR1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TRAP Alpha/TRAPA/SSR1 Antibody (A06993-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.

IHC analysis of TRAP Alpha/TRAPA/SSR1 using anti-TRAP Alpha/TRAPA/SSR1 antibody (A06993-1).
TRAP Alpha/TRAPA/SSR1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TRAP Alpha/TRAPA/SSR1 Antibody (A06993-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.

IHC analysis of TRAP Alpha/TRAPA/SSR1 using anti-TRAP Alpha/TRAPA/SSR1 antibody (A06993-1).
TRAP Alpha/TRAPA/SSR1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TRAP Alpha/TRAPA/SSR1 Antibody (A06993-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.

IHC analysis of TRAP Alpha/TRAPA/SSR1 using anti-TRAP Alpha/TRAPA/SSR1 antibody (A06993-1).
TRAP Alpha/TRAPA/SSR1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TRAP Alpha/TRAPA/SSR1 Antibody (A06993-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.

IHC analysis of TRAP Alpha/TRAPA/SSR1 using anti-TRAP Alpha/TRAPA/SSR1 antibody (A06993-1).
TRAP Alpha/TRAPA/SSR1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TRAP Alpha/TRAPA/SSR1 Antibody (A06993-1) overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB as the chromogen.

IF analysis of TRAP Alpha/TRAPA/SSR1 using anti-TRAP Alpha/TRAPA/SSR1 antibody (A06993-1).
TRAP Alpha/TRAPA/SSR1 was detected in an immunocytochemical section of U20S cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-TRAP Alpha/TRAPA/SSR1 Antibody (A06993-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.

Immunoprecipitating (IP) SSR1 in HepG2 whole cell lysate.
Western blot analysis of SSR1 using anti-SSR1 antibody (A06993-1);
Lane 1: HepG2 whole cell lysates (30ug);
Lane 2: Rabbit control IgG instead of anti-SSR1 antibody in HepG2 whole cell lysate;
Lane 3: anti-SSR1 antibody (2μg) + HepG2 whole cell lysate (500μg).
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-SSR1 antigen affinity purified polyclonal antibody (A06993-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for SSR1 at approximately 36 kDa. The expected band size for SSR1 is at 32 kDa.

Flow Cytometry analysis of K562 cells using anti-TRAP Alpha/TRAPA/SSR1 antibody (A06993-1).
Overlay histogram showing K562 cells stained with A06993-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TRAP Alpha/TRAPA/SSR1 Antibody (A06993-1, 1 μg/1x10⁶ cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x10⁶ cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x10⁶) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.