Cell viability assay was performed by the CellTiter-Glo Luminescent Cell Viability Assay Kit (Promega). For MI-503 treatment, T47D or MCF-7 cells were seeded in 96-well plate with 200 cells per well and treated with DMSO or MI-503 for 3 days. For circulated cells, 2000 cells after circulation were seeded in 50 μL of medium in 96-well plates. The assay reagent mixture was directly added into the cell medium at a 1:1 ratio for 15 min to lyse the cells, and the luminescent signal was detected using the Thermo Luminoskan Ascent Microplate Reader (Thermo Fisher Scientific).
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.