Western blot (WB): | 1:500-2000 |
Figure 1. Western blot analysis of Cyclin B1/CCNB1 using anti-Cyclin B1/CCNB1 antibody (BA0766-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat brain tissue lysates,
Lane 2: rat thymus tissue lysates,
Lane 3: rat placenta tissue lysates,
Lane 4: rat spleen tissue lysates,
Lane 5: human Raji whole cell lysates,
Lane 6: human MCF-7 whole cell lysates,
Lane 7: human COLO320 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Cyclin B1/CCNB1 antigen affinity purified polyclonal antibody (BA0766-2) 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 Cyclin B1/CCNB1 at approximately 55 kDa. The expected band size for Cyclin B1/CCNB1 is at 48 kDa.
Figure 2. Western blot analysis of Cyclin B1/CCNB1 using anti-Cyclin B1/CCNB1 antibody (BA0766-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat testis tissue lysates,
Lane 2: rat ovary tissue lysates,
Lane 3: rat thymus tissue lysates,
Lane 4: rat spleen tissue lysates,
Lane 5: human Hela whole cell lysates,
Lane 6: human 293T whole cell lysates,
Lane 7: human SW620 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Cyclin B1/CCNB1 antigen affinity purified polyclonal antibody (BA0766-2) 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 Cyclin B1/CCNB1 at approximately 55 kDa. The expected band size for Cyclin B1/CCNB1 is at 48 kDa.
Figure 1. Western blot analysis of Cyclin B1/CCNB1 using anti-Cyclin B1/CCNB1 antibody (BA0766-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat brain tissue lysates,
Lane 2: rat thymus tissue lysates,
Lane 3: rat placenta tissue lysates,
Lane 4: rat spleen tissue lysates,
Lane 5: human Raji whole cell lysates,
Lane 6: human MCF-7 whole cell lysates,
Lane 7: human COLO320 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Cyclin B1/CCNB1 antigen affinity purified polyclonal antibody (BA0766-2) 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 Cyclin B1/CCNB1 at approximately 55 kDa. The expected band size for Cyclin B1/CCNB1 is at 48 kDa.
Figure 2. Western blot analysis of Cyclin B1/CCNB1 using anti-Cyclin B1/CCNB1 antibody (BA0766-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat testis tissue lysates,
Lane 2: rat ovary tissue lysates,
Lane 3: rat thymus tissue lysates,
Lane 4: rat spleen tissue lysates,
Lane 5: human Hela whole cell lysates,
Lane 6: human 293T whole cell lysates,
Lane 7: human SW620 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Cyclin B1/CCNB1 antigen affinity purified polyclonal antibody (BA0766-2) 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 Cyclin B1/CCNB1 at approximately 55 kDa. The expected band size for Cyclin B1/CCNB1 is at 48 kDa.