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. 2013 Jan 31;8(1):e54664. doi: 10.1371/journal.pone.0054664

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© 2013 Valencia-Cruz et al

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.

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Inline graphic — Superoxide radical was measured by flow cytometry with MitoSox (FL2-H channel) dye; SSCH corresponds to side scatter channel. Panel A: untreated HeLa cells, Panel B: Cas/HeLa, Panel C: untreated CHP-212 cells, panel D: Cas/CHP-212. Positive controls, are 3 h UV-irradiated cells. Data is representative of three independent experiments for each experimental condition.

Superoxide radical was measured by flow cytometry with MitoSox (FL2-H channel) dye; SSCH corresponds to side scatter channel. Panel A: untreated HeLa cells, Panel B: Cas/HeLa, Panel C: untreated CHP-212 cells, panel D: Cas/CHP-212. Positive controls, are 3 h UV-irradiated cells. Data is representative of three independent experiments for each experimental condition.