Application
Wild-type (WT) and MSH6 knockout (KO) HeLa cell extracts (30 µg) were separated by 5% SDS-PAGE, and the membrane was blotted with MSH6 antibody [C1C2], Internal diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
Application
MSH6 antibody [C1C2], Internal detects MSH6 protein by Western blot analysis. A. 30 µg Neuro2A whole cell lysate/extract B. 30 µg GL261 whole cell lysate/extract 5% SDS-PAGE MSH6 antibody [C1C2], Internal dilution: 1:1000
Application
Immunofluorescence analysis of paraformaldehyde-fixed HeLa, using GTBP (MSH6) antibody at 1:500 dilution.
Application
Immunohistochemical analysis of paraffin-embedded NCIN87 Xenograft, using GTBP (MSH6) antibody at 1:100 dilution.
Application
Sample (30 ug of whole cell lysate) A: Hep G2 5% SDS PAGE diluted at 1:1000
Application
MSH6 antibody [C1C2], Internal immunoprecipitates MSH6 protein in IP experiments. IP samples: 293T whole cell extract A. 40 μg 293T whole cell extract B. Control with 4 μg of preimmune Rabbit IgG C. Immunoprecipitation of MSH6 protein by 4 μg MSH6 antibody [C1C2], Internal 5 % SDS-PAGE The immunoprecipitated MSH6 protein was detected by MSH6 antibody [C1C2], Internal diluted at 1:1000. [EasyBlot anti-rabbit IgG was used as a secondary reagent]