Figure 6. Caspase-3 was activated following the treatments.
Cells were subjected to treatments with sodium azide/2-DG, increased temperature or combination of sodium azide/2-DG plus increased temperature for a period of 30 minute or 1 hour. Control cells received no treatment. Cleavage of caspase-3 and PARP-1 were analyzed with western blot. β-actin was used as a loading control.