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. Author manuscript; available in PMC: 2009 Mar 1.
Published in final edited form as: Free Radic Biol Med. 2007 Dec 8;44(5):868–881. doi: 10.1016/j.freeradbiomed.2007.11.020

Fig. 4. Effect of GFP-tagged wild-type and kinase-dead c-Abl on H2O2-NOX5 regulation.

Fig. 4

Superoxide production was determined in the presence or absence of 100 μM H2O2. (A) K562 cells stably expressing GFP-c-Abl or GFP-KD-c-Abl were transfected with the pRep4 vector encoding the NOX5 protein. (B) HEK/NOX5 cells transiently transfected with either an empty vector or the wild-type c-Abl or kinase-dead c-Abl. Superoxide production was expressed as a percent of the value obtained for non-treated cells in the absence of H2O2. The data are the means +/− SEM of 3 to 4 independent experiments. Asterisks indicate statistical significance versus control cells without H2O2 * P < 0.05; ** P <0.01, Numbers above the first column of each graph represent the mean +/− SEM of the chemiluminescence output observed in those samples at 10 minutes.

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