Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-200 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-200 |
Flow Cytometry (FCM): | 1:50 |
Figure 1. Western blot analysis of anti-ATM antibody (BM4091). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human HepG2 whole cell lysates,
Lane 2: human 293T whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ATM antigen affinity purified monoclonal antibody (BM4091) 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 ATM at approximately 351 kDa. The expected band size for ATM is at 351 kDa.
Immunohistochemical analysis of paraffin-embedded human breast cancer, using ATM Antibody.
Immunofluorescent analysis of Hela cells, using ATM Antibody.
Figure 1. Western blot analysis of anti-ATM antibody (BM4091). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human HepG2 whole cell lysates,
Lane 2: human 293T whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ATM antigen affinity purified monoclonal antibody (BM4091) 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 ATM at approximately 351 kDa. The expected band size for ATM is at 351 kDa.
Immunohistochemical analysis of paraffin-embedded human breast cancer, using ATM Antibody.
Immunofluorescent analysis of Hela cells, using ATM Antibody.