Application
Non-transfected (–) and transfected (+) HT-29 whole cell extracts (30 µg) were separated by 12% SDS-PAGE, and the membrane was blotted with HSP27 antibody diluted at 1:10000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
Application
Wild-type (WT) and HSP27 knownout (KO) HeLa cell extracts (30 µg) were separated by 12% SDS-PAGE, and the membrane was blotted with HSP27 antibody diluted at 1:20000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
Application
Various whole cell extracts (30 µg) were separated by 12% SDS-PAGE, and the membrane was blotted with HSP27 antibody diluted at 1:10000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
Application
HSP27 antibody detects HSP27 protein at cytoplasm and cytoskeleton by immunofluorescent analysis. Sample: HeLa cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: HSP27 protein stained by HSP27 antibody diluted at 1:1000. Red: phalloidin, a cytoskeleton marker, stained by phalloidin (invitrogen, A12380) diluted at 1:200. Blue: Hoechst 33342 staining.
Application
HSP27 antibody detects HSP27 protein at cytoplasm in human lung papillary carcinoma by immunohistochemical analysis. Sample: Paraffin-embedded human lung papillary carcinoma. HSP27 antibody diluted at 1:500.
Application
Immunoprecipitation of HSP27 protein from HeLa whole cell extracts using 5 μg of HSP27 antibody . Western blot analysis was performed using HSP27 antibody . EasyBlot anti-Rabbit IgG was used as a secondary reagent.
Application
Sample (50 µg of whole cell lysate) A: mouse liver 12% SDS PAGE diluted at 1:1000 The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.