Application
Immunoprecipitation of ATR protein from HCT-116 whole cell extracts treated with 2 mM Hydroxyurea 6 hrs using 5 μg of ATR antibody or ATR antibody . Western blot analysis was performed using ATR antibody . EasyBlot anti-Mouse IgG was used as a secondary reagent.
Application
Untreated (–) and treated (+) HCT116 whole cell extracts (30 µg) were separated by 5% SDS-PAGE, and the membrane was blotted with ATR (phospho Thr1989) antibody [GT222] diluted at 1:500. The signal was developed with Trident ECL plus-Enhanced.