Colorimetric cytotoxicity detection
Fluorometric detection of viable and dead cells
Fluorometric detection of viable and dead eukaryotic cells
For discrimination between live and dead cells by flow cytometry or fluorescence microscopy. Available with unique, cell membrane-impermeable dyse that specifically stain the nuclei of dead cells.
For studying the regulation of lysosomal cytotoxicity in cultured cells by using fluorescence microscopy and flow cytometry.
(3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide); tetrazolium derivative used widely in cell viability and proliferation testing
This kit offers an excellent and efficient method for in vitro cytotoxicity studies as well as high-throughput drug screening.
Product bundle consisting of our Mononuclear Cell Medium, animal/endotoxin-free human IL-2 and the ready-to-use Cell Proliferation Kit I (CFSE).
Can be used for measuring cell proliferation and mitochondrial metabolic activity.
Specific detection of senescence marker in distinct pH in cultured cells and tissue sections.
Simple, sensitive, one-step assay to measure senescence cells using FACS.
The colorimetric sulforhodamine B (SRB) assay is one of the most widely methods used to detect cell viability or drug cytotoxicity.
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