Western blot analysis of extracts of various cell lines, using Anti-Caspase-3 Antibody (A93187) at 1:1,000 dilution. Jurkat cells were treated by staurosporine(1 uM) for 3 hour. The secondary antibody was Goat Anti-Rabbit IgG H&L Antibody (HRP) at 1:10,000 dilution. Lysates/proteins were present at 25µg per lane. The blocking buffer used was 3% non-fat dry milk in TBST. Detection was with a ECL Basic Kit. Exposure time: 90s.
Western blot analysis of extracts from normal (control) and Caspase-3 knockout (KO) 293T cells, using Anti-Caspase-3 Antibody (A93187) at 1:1,000 dilution. The secondary antibody was Goat Anti-Rabbit IgG H&L Antibody (HRP) at 1:10,000 dilution. Lysates/proteins were present at 25µg per lane. The blocking buffer used was 3% non-fat dry milk in TBST. Detection was with a ECL Basic Kit. Exposure time: 90s.
Immunofluorescence analysis of Jurkat cells using Anti-Caspase-3 Antibody (A93187) at a dilution of 1:100 (40x lens). DAPI was used to stain the cell nuclei (blue).
Immunofluorescence analysis of RAW264. 7 cells using Anti-Caspase-3 Antibody (A93187) at a dilution of 1:100 (40x lens). DAPI was used to stain the cell nuclei (blue).
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