The cells were fixed with 3.5% formaldehyde solution for 10 min, rinsed twice with phosphate-buffered saline (PBS), and incubated with 1.5% Oil Red O in 60% isopropanol (O0625; Sigma-Aldrich) for 1 h. The cells were washed three times with PBS and dried to observe lipid droplets. For quantification of differentiated cells, stained Oil Red O was dissolved in dimethyl sulfoxide and its absorbance was measured at 510 nm.
Do you have any questions about this protocol?
Post your question to gather feedback from the community. We will also invite the authors of this article to respond.