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. Author manuscript; available in PMC: 2012 Aug 30.
Published in final edited form as: Toxicon. 2010 Jul 24;56(6):1025–1034. doi: 10.1016/j.toxicon.2010.07.007

Fig. 6.

Fig. 6

drice knockdown prevents PE-mediated increase in caspase activity. S2 cells were subjected to RNAi using dsRNA to drice followed by incubation in the presence of 50ng/ml PE or 150ng/ml actinomycin D for 24 h. An increase in the Drice activity was estimated by measuring the increase in fluorescence upon hydrolysis of DEVD-AFC. The specific caspase activity of the dsRNA to drice-treated samples is presented as the fold-change value compared to the untreated sample. Each bar is the mean of at least three determinations. Error bars represent standard deviation of the mean.