Application
p21 Cip1 antibody [GT1032] detects p21 Cip1 protein at nucleus by immunofluorescent analysis. Sample: HCT116 cells treated with 30μM cisplatin for 24hr and were fixed in 4% paraformaldehyde at RT for 15 min. Green: p21 Cip1 protein stained by p21 Cip1 antibody [GT1032] diluted at 1:500. Blue: Hoechst 33342 staining.
Application
Wild-type (WT) and p21 Cip1 knockout (KO) HeLa cell extracts (30 µg) were separated by 15% SDS-PAGE, and the membrane was blotted with p21 Cip1 antibody [GT1032] diluted at 1:500. The HRP-conjugated anti-mouse IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.
Application
p21 Cip1 antibody [GT1032] detects p21 Cip1 protein by western blot analysis. A. 30 µg HCT116 whole cell lysate/extract (untreated) B. 30 µg HCT116 whole cell lysate/extract (30 µM Cisplatin treatment for 24 hr) C. 30 µg HCT116 whole cell lysate/extract (30 µM Cisplatin treatment for 48 hr) 15% SDS-PAGE p21 Cip1 antibody [GT1032] dilution: 1:1000 The HRP-conjugated anti-mouse IgG antibody was used to detect the primary antibody.
Application
p21 Cip1 antibody [GT1032] immunoprecipitates CDKN1A protein in IP experiments. IP samples: HCT-116 whole cell extract treat with 30uM cisplatin for 48 hr A. 30 μg HCT-116 whole cell extract treat with 30uM cisplatin for 48 hr B. Control with 4 μg of preimmune Mouse IgG C. Immunoprecipitation of CDKN1A protein by 4 μg p21 Cip1 antibody [GT1032] 15 % SDS-PAGE The immunoprecipitated CDKN1A protein was detected by p21 Cip1 antibody [GT1032] diluted at 1:1000. [EasyBlot anti-mouse IgG was used as a secondary reagent]
Application
p21 Cip1 antibody [GT1032] detects p21 Cip1 protein at nucleus by immunofluorescent analysis. Sample: MCF7 cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: CDK4 protein stained by CDK4 antibody diluted at 1:1000. Red: p21 Cip1 protein stained by p21 Cip1 antibody [GT1032] diluted at 1:500. Blue: Hoechst 33342 staining.