2.7. MTS Proliferation Assay

DG Dean Gilham
AS Audrey L. Smith
LF Li Fu
DM Dalia Y. Moore
AM Abenaya Muralidharan
SR St. Patrick M. Reid
SS Stephanie C. Stotz
JJ Jan O. Johansson
MS Michael Sweeney
NW Norman C. W. Wong
EK Ewelina Kulikowski
DE Dalia El-Gamal
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3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS) assays were used to determine BETi-induced cytotoxicity. Briefly, Calu-3 (~20,000 cells/well), Vero E6 (~10,000/well), or Karpas-299 (~20,000 cells/well) were treated with vehicle (DMSO) or increasing amounts of BETi for 48 h in 96-well plates, and then, the CellTiter 96® AQueous assay (Promega, Madison, WI, USA) was preformed according to the manufacturer’s instructions to determine cell proliferation. Absorbance signals from each well were acquired at 490 nm on a Tecan Infinite® M1000 Pro microplate reader (Männedorf, Switzerland).

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