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Flow Cytometry analysis of A549 cells using anti-Human Bax antibody (A00183-Dyl488).
Product group Antibodies
Boster Bio
Anti-Human Bax DyLight 488 conjugated AntibodyA00183-Dyl488
Boster Kit Box
Product group Antibodies
Boster Bio
Anti-Human Bax DyLight 550 conjugated AntibodyA00183-Dyl550
IHC analysis of Bax using anti-Bax antibody (A00183). Bax was detected in paraffin-embedded section of human lung cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Bax Antibody (A00183) 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.
Product group Antibodies
Boster Bio
Anti-Bax Picoband AntibodyA00183
Product group Antibodies
Boster Bio
Anti-HLA-B AntibodyA00186-1
Western blot analysis of MUC1 using anti-MUC1 antibody (A00187). 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 50ug of sample under reducing conditions. Lane 1: rat lung tissue lysates, Lane 2: rat pancreas tissue lysates, Lane 3: mouse pancreas tissue lysates. After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA 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-MUC1 antigen affinity purified polyclonal antibody (Catalog # A00187) at 0.5 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 1:10000 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 MUC1 at approximately 122KD. The expected band size for MUC1 is at 122KD.
Product group Antibodies
Boster Bio
Anti-MUC1 AntibodyA00187
Product group Antibodies
Boster Bio
Anti-Flt3 / CD135 AntibodyA00188-3
IHC analysis of Flt3 / CD135 using anti-Flt3 / CD135 antibody (A00188-4). Flt3 / CD135 was detected in paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-Flt3 / CD135 Antibody (A00188-4) overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
Product group Antibodies
Boster Bio
Anti-Flt3 / CD135 AntibodyA00188-4
IHC analysis of CD80 using anti-CD80 antibody (A00196-1).
Product group Antibodies
Boster Bio
Anti-CD80 AntibodyA00196-1
Western blot analysis of TLR3 using anti-TLR3 antibody (A00197).
Product group Antibodies
Boster Bio
Anti-TLR3 AntibodyA00197
IHC analysis of Ran using anti-Ran antibody (A00204-1). Ran was detected in paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-Ran Antibody (A00204-1) 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.
Product group Antibodies
Boster Bio
Anti-Ran AntibodyA00204-1
Western blot analysis of CD86 using anti-CD86 antibody (A00220-1). 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 50ug of sample under reducing conditions. Lane 1: rat spleen tissue lysate, Lane 2: rat liver tissue lysate, Lane 3: rat PC-12 cell lysate, Lane 4: mouse spleen tissue lysate, Lane 5: mouse thymus tissue lysate, Lane 6: mouse brain tissue lysate, Lane 7: human COLO-320 cell lysate. After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA 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-CD86 antigen affinity purified polyclonal antibody (Catalog # A00220-1) at 0.5 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 1:10000 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 CD86 at approximately 60-80KD. The expected band size for CD86 is at 36KD.
Product group Antibodies
Boster Bio
Anti-CD86 AntibodyA00220-1
IHC analysis of SRI using anti-SRI antibody (A00222). SRI was detected in paraffin-embedded section of human intestinal cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/ml rabbit anti-SRI Antibody (A00222) 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.
Product group Antibodies
Boster Bio
Anti-SRI AntibodyA00222
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