Homogeneous, colorimetric cell viability assay; requires mixing of MTS and PMS components prior to assay, then a 1- to 4-hour incubation. Standalone MTS powder for applications where optimization of assay for specific cell types or conditions is desired.
The CytoTox-Fluor Cytotoxicity Assay is a single-reagent-addition, homogeneous, fluorescent assay that measures the relative number of dead cells in cell populations.
A fast homogeneous, fluorometric method for estimating the number of non-viable cells present in multiwell plates. Based on detection of LDH release, an indicator of cytotoxicity.
The Viral ToxGlo™ Assay is a simple, quantifiable method of determining viral-induced cytopathic effects (CPE) in host cells caused by lytic virions. The assay measures cellular ATP as a surrogate measure of host cell viability.
Colorimetric assay for the determination of cell membrane integrity based on detection of LDH release, an indicator of cytotoxicity. Sample transfer steps are required.
pHAb Amine Reactive Dye exhibits very low fluorescence at pH > 7 and much higher fluorescence as the pH of the solution becomes acidic. pHAb Dyes are designed specifically for antibody labeling.
The ApoTox-Glo™ Triplex Assay combines three assay chemistries to easily assess viability, cytotoxicity and apoptosis events in the same cell-based assay well.
The ApoLive-Glo™ Multiplex Assay measures both the number of viable cells as a marker of cytotoxicity and caspase activation as a marker of apoptosis within a single assay well to determine the mechanism of cell death.
CellTiter 96(R) AQueous MTS Reagent Powder is a novel tetrazolium compound for use in colorimetric assays to determine the number of viable cells in proliferation, cytotoxicity or chemosensitivity assays.
The RealTime-Glo™ MT Cell Viability Assay is a non-lytic, homogeneous, bioluminescent method to determine in real time the number of viable cells in culture by measuring the reducing potential of cells and thus metabolism (MT).