Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-200 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-200 |
ImmunoPrecipitation (IP): | 1:30 |
Flow Cytometry (FCM): | 1:50 |
Figure 1. Western blot analysis of anti-BAD antibody (BM4241). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human Hela whole cell lysates,
Lane 2: human MCF-7 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-BAD antigen affinity purified monoclonal antibody (BM4241) 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 BAD at approximately 23 kDa. The expected band size for BAD is at 18 kDa.
All lanes use the Antibody for 1 hour at room temperature.
Immunohistochemical analysis of paraffin-embedded human colon cancer, using Bad Antibody.
Immunofluorescent analysis of Hela cells, using Bad Antibody .
Figure 1. Western blot analysis of anti-BAD antibody (BM4241). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human Hela whole cell lysates,
Lane 2: human MCF-7 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-BAD antigen affinity purified monoclonal antibody (BM4241) 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 BAD at approximately 23 kDa. The expected band size for BAD is at 18 kDa.
All lanes use the Antibody for 1 hour at room temperature.
Immunohistochemical analysis of paraffin-embedded human colon cancer, using Bad Antibody.
Immunofluorescent analysis of Hela cells, using Bad Antibody .