After treatment, 2×105 cells were incubated with Rho123 dye at a final concentration of 10 μM for 90 min. After incubation, the cells were harvested and washed twice with ice-cold PBS, and then resuspended in PBS. The fluorescence intensity of the cells was determined using a FACS Calibur flow cytometer (Becton Dickinson, San Jose, CA, USA).
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