After hormonal treatment for 24 h, the MTT assay was performed. In summary, cell culture supernatants were removed and a solution was added to each plate containing 100 μl of fresh medium DMEM F12 with 10 μl of an MTT solution (Calbiochem, Darmstadt, Germany) of 5 mg/mL in PBS, resulting in a final MTT concentration of 0.5 mg/ml. Cells were maintained in the incubator for 3 h until blue crystals were formed. At this point, DMSO (100 μl) was added to dissolve the crystals, the plate was homogenized, and absorbance reading was performed at 570 nm in a spectrophotometer.
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.