Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Enzyme linked immunosorbent assay (ELISA): | 1:100-1000 |
Flow Cytometry (Fixed): | 1:50-200 |
Western blot analysis of BCRP/ABCG2 using anti-BCRP/ABCG2 antibody (A00457-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human A549 whole cell lysates,
Lane 2: human MDA-MB-453 whole cell lysates,
Lane 3: human HepG2 whole cell lysates,
Lane 4: human CACO-2 whole cell lysates,
Lane 5: human PC-3 whole cell lysates,
Lane 6: Rat liver tissue lysates,
Lane 7: Rat kidney tissue lysates,
Lane 8: Mouse HEPA1-6 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-BCRP/ABCG2 antigen affinity purified polyclonal antibody (A00457-2) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for BCRP/ABCG2 at approximately 65-80 kDa. The expected band size for BCRP/ABCG2 is at 72 kDa.
IHC analysis of BCRP/ABCG2 using anti-BCRP/ABCG2 antibody (A00457-2).
BCRP/ABCG2 was detected in a paraffin-embedded section of human mammary cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-BCRP/ABCG2 Antibody (A00457-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of BCRP/ABCG2 using anti-BCRP/ABCG2 antibody (A00457-2).
BCRP/ABCG2 was detected in a paraffin-embedded section of mouse liver tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-BCRP/ABCG2 Antibody (A00457-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
Flow Cytometry analysis of SiHa cells using anti-BCRP/ABCG2 antibody (A00457-2).
Overlay histogram showing SiHa cells stained with A00457-2 (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-BCRP/ABCG2 Antibody (A00457-2) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
Western blot analysis of BCRP/ABCG2 using anti-BCRP/ABCG2 antibody (A00457-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human A549 whole cell lysates,
Lane 2: human MDA-MB-453 whole cell lysates,
Lane 3: human HepG2 whole cell lysates,
Lane 4: human CACO-2 whole cell lysates,
Lane 5: human PC-3 whole cell lysates,
Lane 6: Rat liver tissue lysates,
Lane 7: Rat kidney tissue lysates,
Lane 8: Mouse HEPA1-6 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-BCRP/ABCG2 antigen affinity purified polyclonal antibody (A00457-2) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for BCRP/ABCG2 at approximately 65-80 kDa. The expected band size for BCRP/ABCG2 is at 72 kDa.
IHC analysis of BCRP/ABCG2 using anti-BCRP/ABCG2 antibody (A00457-2).
BCRP/ABCG2 was detected in a paraffin-embedded section of human mammary cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-BCRP/ABCG2 Antibody (A00457-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of BCRP/ABCG2 using anti-BCRP/ABCG2 antibody (A00457-2).
BCRP/ABCG2 was detected in a paraffin-embedded section of mouse liver tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-BCRP/ABCG2 Antibody (A00457-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
Flow Cytometry analysis of SiHa cells using anti-BCRP/ABCG2 antibody (A00457-2).
Overlay histogram showing SiHa cells stained with A00457-2 (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-BCRP/ABCG2 Antibody (A00457-2) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.