Application
Aurora A antibody [C3], C-term detects AURKA protein by western blot analysis. A. 30 µg PC-12 whole cell lysate/extract 10% SDS-PAGE Aurora A antibody [C3], C-term dilution: 1:1000 The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
Application
Aurora A antibody [C3], C-term detects AURKA protein by western blot analysis. A. 30 µg Neuro2A whole cell lysate/extract B. 30 µg GL261 whole cell lysate/extract 10% SDS-PAGE Aurora A antibody [C3], C-term dilution: 1:1000 The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
Application
Aurora A antibody [C3], C-term detects AURKA protein by western blot analysis. A. 30 µg 293T whole cell lysate/extract B. 30 µg A431 whole cell lysate/extract C. 30 µg HeLa whole cell lysate/extract D. 30 µg HepG2 whole cell lysate/extract E. 30 µg A375 whole cell lysate/extract 10% SDS-PAGE Aurora A antibody [C3], C-term dilution: 1:1000 The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
Application
Immunohistochemical analysis of paraffin-embedded TW2.6 xenograft, using Aurora A antibody at 1:100 dilution.
Application
Confocal immunofluorescence analysis (Olympus FV10i) of paraformaldehyde-fixed U2OS, using Aurora A antibody (Green) at 1:500 dilution. Alpha-tubulin filaments were labeled with (Red) at 1:100.
Application
Confocal immunofluorescence analysis (Olympus FV10i) of methanol-fixed 293T, using Aurora A antibody (Green) at 1:100 dilution. Alpha-tubulin filaments were labeled with (Red) at 1:2500.
Application
Aurora A antibody [C3], C-term immunoprecipitates Aurora A protein in IP experiments. IP samples: 293T whole cell extract A. Control with 4 μg of preimmune Rabbit IgG B. Immunoprecipitation of Aurora A protein by 4 μg Aurora A antibody [C3], C-term 10 % SDS-PAGE The immunoprecipitated Aurora A protein was detected by Aurora A antibody [C3], C-term diluted at 1:500. [EasyBlot anti-rabbit IgG was used as a secondary reagent]