Fig. 1
From: Antioxidant and skin protection effect of morin upon UVA exposure
Analysis of cytotoxic effects of morin on HDFs. Cells were inoculated in 96-well plates at a concentration of 3 × 103 cells/well and incubated for 24 h. Morin was added to the wells and cultured for an additional 24 h. Ten microliters of EZ-Cytox cell viability assay kit reagent (ItsBio, South Korea) was added to the incubated cell culture dish, and the absorbance was measured at 490 nm using a microplate reader (Bio-Rad, USA). The mean and standard deviation of cell viability were determined