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Cell viability was assessed 3 days after treatment with FOXO4-DRI at 0, 12.5, 25, 50, and 100 M, respectively, using the Cell Counting Kit-8 (CCK-8) Assay (Dojindo, Rockville, MD, United States)
The excitation filter for CFP was 430/20 nm and emission filters for CFP and YFP were 485/20 nm and 535 nm/25 nm, respectively in microplate reader

Antioxidants 10:1256

cFLIP suppression and DR5 activation sensitize senescent cancer cells to senolysis
