Whole LDH was made by introducing lysis buffer to liberate all cytoplasmic LDH. Cell viability was calculated with proportion of overall LDH. For the PI staining, Cells were being treated with indicated stimulus and afterwards PI (5 μg/mL) was immediately additional to medium and incubated for 20 min. The pictures https://fletcherb701gko8.buscawiki.com/user