In vitro cytotoxicity was measured by an MTT assay. HepG2, Huh-7, SMMC-7721, HCC-LM3, HLE and LX2 cells were seeded in 96-well plates at a density of 1 × 104 cells/well for 24 h. Afterwards, different concentrations of ginsenoside CK (2.5–100 μM) and CoCl2 (50–500 μM) were added. After incubating for an additional 48 h, MTT (0.5 mg/mL) was added and cultured for 2–4 h. Finally, MTT was removed carefully followed by addition of 150 μL DMSO to each well, and the plates were detected by a microplate reader (Bio-Tek Instruments, Inc., Winooski, VT, USA) at 490 nm. Each data point was an average of the values of six replicates at each concentration.
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.