Provides a standardized fluorometric method for sensitive quantification of viable cells in 3D cell culture.
Can be incorporated into DNA during cell division and used to study cell-cycle kinetics.
Highly sensitive, high-throughput adaptable colorimetric assay to detect acid phosphatase (AP) activity as a direct correlation of cell cytotoxicity.
Bioluminescent cytotoxicity detection
Allows to study the regulation of autophagy and cytotoxicity in cultured cells by fluorescence microscopy and flow cytometry.
Fluorometric detection of viable and dead bacteria
This kit utilizes bioluminescent detection of the ATP level for a rapid screening of apoptosis and cell viability in mammalian cells.
Assay for detecting ADP/ATP ratios for a rapid screening of apoptosis/necrosis/growth arrest/cell proliferation simultaneously in mammalian cells
Flow cytometry-based method to detect and monitor cells at various stages of the cell cycle.
Mitochondrial Permeability Transition Pore Assay for distinguishing between dead & healthy cells
For flow cytometry or microscopy
Convenient, highly sensitive colorimetric assay that is adaptable to high throughput.
Convenient, highly sensitive and non-radioactive proliferation assay for flow cytometry. Available containing different fluorophores.
Convenient, highly sensitive and non-radioactive proliferation assay for fluorescence microscopy. Available containing different fluorophores.
Convenient, fast, highly sensitive and high throughput-adaptable proliferation assay. Available with different fluorophores.
Highly sensitive, fluorometric assay detecting as less as 30 proliferating or necrotic cells.
Colorimetric cell viability and cytotoxicity detection
Cell Proliferation & Cytotoxicity Assay Kit
This colorimetric assay is one of the common methods used to detect cell viability or drug cytotoxicity.
Fluorometric cell viability and cytotoxicity detection.
Sensitive fluorescent measurement of released LDH in culture medium.
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.
(2,3-Bis-(2-Methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide, disodium salt); tetrazolium derivative used widely in cell viability and proliferation testing
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