Western blot (WB): | 1:500-2000 |
Figure 1. Western blot analysis of ATM using anti-ATM antibody (BA0655-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Rat Testis tissue lysates ,
Lane 2: U87 whole cell lysates ,
Lane 3: MCF-7 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ATM antigen affinity purified polyclonal antibody (BA0655-2) 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 ATM at approximately 350 kDa. The expected band size for ATM is at 351 kDa.
Figure 2. Western blot analysis of ATM using anti-ATM antibody (BA0655-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: HELA whole cell lysates ,
Lane 2: SMMC whole cell lysates ,
Lane 3: U87 whole cell lysates ,
Lane 4: A549 whole cell lysates ,
Lane 5: MCF-7 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ATM antigen affinity purified polyclonal antibody (BA0655-2) 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 ATM at approximately 350 kDa. The expected band size for ATM is at 351 kDa.
Figure 1. Western blot analysis of ATM using anti-ATM antibody (BA0655-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Rat Testis tissue lysates ,
Lane 2: U87 whole cell lysates ,
Lane 3: MCF-7 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ATM antigen affinity purified polyclonal antibody (BA0655-2) 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 ATM at approximately 350 kDa. The expected band size for ATM is at 351 kDa.
Figure 2. Western blot analysis of ATM using anti-ATM antibody (BA0655-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: HELA whole cell lysates ,
Lane 2: SMMC whole cell lysates ,
Lane 3: U87 whole cell lysates ,
Lane 4: A549 whole cell lysates ,
Lane 5: MCF-7 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ATM antigen affinity purified polyclonal antibody (BA0655-2) 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 ATM at approximately 350 kDa. The expected band size for ATM is at 351 kDa.