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Viability Assays for Cells in Culture
Published on: January 20, 2014
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A Luminescence Assay to Quantify Cell Viability in Real Time
Peter Hofsteen1, Natasha Karassina1, James J Cali1
1Research and Development, Promega Corporation, Madison, WI, USA.
Methods in Molecular Biology (Clifton, N.J.)
|May 25, 2021
Summary
This study introduces a novel live-cell assay for real-time monitoring of cell viability and drug-induced cytotoxicity. The assay enables continuous tracking of cellular responses over days, preserving cells for further analysis.
Area of Science:
- Cell Biology
- Pharmacology
- Biotechnology
Background:
- Understanding cellular responses to environmental changes or drug treatments necessitates time-dependent analysis.
- Existing methods may not offer continuous monitoring or cell preservation for downstream applications.
Purpose of the Study:
- To develop a sensitive, nonlytic live-cell assay for real-time monitoring of cell viability, growth, and cytotoxicity.
- To demonstrate the assay's utility in drug-dependent cytotoxicity studies using cancer cells.
Main Methods:
- A novel live-cell assay enabling continuous monitoring of cellular parameters.
- Application of the assay in 384-well plates for drug and antibody-dependent cytotoxicity studies.
- Real-time measurement of cell viability, growth, and cytotoxicity.
Main Results:
- The assay provides continuous, real-time data on cellular status over extended periods (hours to days).
- Demonstrated successful application in small molecule and antibody-dependent cytotoxicity studies.
- Confirmed preservation of cells for subsequent multiplexing with other applications.
Conclusions:
- The developed live-cell assay offers a sensitive and nonlytic method for comprehensive, time-dependent analysis of cellular responses.
- This real-time monitoring approach provides valuable insights into drug mechanisms of action and cellular health.
- The assay's ability to preserve cells enhances its utility for integrated biological studies.

