Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Flow Cytometry (Fixed): | 1:50-200 |
(Boiling the paraffin sections in 10mM citrate buffer,pH6.0,or PH8.0 EDTA repair liquid for 20 mins is required for the staining of formalin/paraffin sections.) Optimal working dilutions must be determined by end user. |
Western blot analysis of BCRP/ABCG2 using anti-BCRP/ABCG2 antibody (PB9364). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Human Placenta tissue lysates,
Lane 2: HELA whole cell lysates,
Lane 3: PANC whole cell lysates,
Lane 4: COLO320 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 (PB9364) 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 (PB9364).
BCRP/ABCG2 was detected in a paraffin-embedded section of human lung cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-BCRP/ABCG2 Antibody (PB9364) 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 (PB9364).
BCRP/ABCG2 was detected in frozen section of Mouse Kidney tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-BCRP/ABCG2 Antibody (PB9364) 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 (PB9364).
BCRP/ABCG2 was detected in frozen section of rat kidney tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-BCRP/ABCG2 Antibody (PB9364) 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 U-87MG cells using anti-ABCG2 antibody (PB9364).Overlay histogram showing U-87MG cells stained with PB9364 (Blue line).The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ABCG2 Antibody (PB9364, 1:100) for 30 min at 20°C. DyLight488 conjugated goat anti-rabbit IgG (BA1127, 1:100) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1:100) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
Western blot analysis of BCRP/ABCG2 using anti-BCRP/ABCG2 antibody (PB9364). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Human Placenta tissue lysates,
Lane 2: HELA whole cell lysates,
Lane 3: PANC whole cell lysates,
Lane 4: COLO320 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 (PB9364) 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 (PB9364).
BCRP/ABCG2 was detected in a paraffin-embedded section of human lung cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-BCRP/ABCG2 Antibody (PB9364) 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 (PB9364).
BCRP/ABCG2 was detected in frozen section of Mouse Kidney tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-BCRP/ABCG2 Antibody (PB9364) 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 (PB9364).
BCRP/ABCG2 was detected in frozen section of rat kidney tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-BCRP/ABCG2 Antibody (PB9364) 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 U-87MG cells using anti-ABCG2 antibody (PB9364).Overlay histogram showing U-87MG cells stained with PB9364 (Blue line).The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ABCG2 Antibody (PB9364, 1:100) for 30 min at 20°C. DyLight488 conjugated goat anti-rabbit IgG (BA1127, 1:100) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1:100) used under the same conditions. Unlabelled sample (Red line) was also used as a control.