Western Blot - Anti-Caspase-3 Antibody [ARC0133] (A308661)
Western blot analysis of various lysates, using Anti-Caspase-3 Antibody [ARC0133] (A308661) 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: 3min.
Western Blot - Anti-Caspase-3 Antibody [ARC0133] (A308661)
Western blot analysis of extracts of Rat liver, using Anti-Caspase-3 Antibody [ARC0133] (A308661) 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: 30s.
Western Blot - Anti-Caspase-3 Antibody [ARC0133] (A308661)
Western blot analysis of extracts of Jurkat, using Anti-Caspase-3 Antibody [ARC0133] (A308661) at 1:1,000 dilution. Jurkat cells were treated by Etoposide (25 uM) at 37°C for 5 hours. 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 - Anti-Caspase-3 Antibody [ARC0133] (A308661)
Western blot analysis of extracts of L929, using Anti-Caspase-3 Antibody [ARC0133] (A308661) at 1:1,000 dilution. L929 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: 180s.
Western Blot - Anti-Caspase-3 Antibody [ARC0133] (A308661)
Western blot analysis of extracts from wild type (WT) and active + pro Caspase 3 knockout (KO) 293T cells, using Anti-Caspase-3 Antibody [ARC0133] (A308661) 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: 10s.
Western Blot - Anti-Caspase-3 Antibody [ARC0133] (A308661)
Western blot analysis of extracts from wild type(WT) and active + pro Caspase-3 knockout (KO) 293T cells, using Anti-Caspase-3 Antibody [ARC0133] (A308661) 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: 30s.
Immunofluorescence analysis of HeLa Treated with Etoposide, HeLa cells using Anti-Caspase-3 Antibody [ARC0133] (A308661) at a dilution of 1:100 (40x lens). DAPI was used to stain the cell nuclei (blue).