First, MDA-MB-231 cells were seeded in 12-well plates, at a density of 3 × 105 cells per well, and allowed to settle overnight. Then, the cells attached to the bottom of the well were scratched to make a wound scratch perpendicular to the marker line. Next, the floating cells were washed off. DMEM was supplemented with various concentrations (0, 2.5, 5, 10 µM) of TSC-3C. The wound scratch was observed exactly at 0, 6, 12, and 24 h. The wound width was measured at different times, and the inhibitory effect of TSC-3C on MDA-MB-231 cell migration was analyzed.
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.