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. Author manuscript; available in PMC: 2011 Sep 1.
Published in final edited form as: FEBS J. 2010 Jul 31;277(17):3575–3587. doi: 10.1111/j.1742-4658.2010.07766.x

Fig. 3.

Fig. 3

ANG enhances Bcl-2 expression, blocks cytochrome c release and inhibits caspase activity. P19 cells were cultured in serum-free medium in the absence or presence of ANG (0.5 µg·mL−1) for the indicated times. (A) Total cell lysates were used for western blotting detection of Bcl-2. The bar graph below the western panel is the relative density of Bcl-2 with β-actin as the normalization control. (B) Cytosolic and mitochondrial proteins were isolated and used for western blotting detection of cytochrome c (Cyto C). The bar graph on the right is the relative abundance of cytochrome c in the cytosol versus that in the mitochondria. (C) Western blotting analysis of pro- and active caspase 3 in the total cell lysate. The bar graph below the western panel is the relative density of Bcl-2 with β-actin as the normalization control. (D) Effect of ANG on caspase activity. Caspase activities were measured using Apo-ONE Caspase 3/7 Reagent.