Previously, we introduced the MultiTox-Fluor Multiplex
Cytotoxicity Assay technology as a novel means for determining the relative
number of live and dead cells in culture. In this article, we demonstrate that
the assay technology is sufficiently scalable, sensitive and robust to be
multiplexed with other downstream assays to increase the quality of screening
Cell Notes 16, 12–15.
Andrew Niles1, Tracy Worzella1, Michael Scurria2, William Daily2, Laurent Bernad2, Pam Guthmiller1, Brian McNamara1, Kay Rashka1, Deborah Lagne1, and Terry L. Riss1