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(A) MV4-11 cells were treated with 200 nM or 1 μM CB-5083 overnight. Cells that were left untreated or treated with 500 mM H2O2 served as control. Induction of apoptosis was assessed by dual staining with Annexin V and 7-AAD. Relative fluorescence of Annexin V and 7-AAD is shown for all conditions. (B) Quantification of the data.
