Homogeneous, colorimetric cell viability assay. Requires a 1- to 4-hour incubation.
CellTiter-Glo™ luminescent cell viability assay involves the addition of a single reagent directly to cells in culture, resulting in cell lysis and the generation of a luminescent signal proportional to the amount of ATP present. ATP is an accepted marker of cell viability. The protocol allows for results in as little as 10 minutes using fewer cells per assay. Each assay kit comes with either one or ten vials of CellTiter-Glo™ buffer and CellTiter-Glo™ lyophilized substrate.
- A Colorimetric Method for Determining the Number of Viable Cells
- Simple "add-mix-measure" format
- Non-radioactive assay
The CellTiter 96 AQueous One Solution Cell Proliferation Assay is a colorimetric method for determining the number of viable cells in proliferation, cytotoxicity or chemosensitivity assays. The CellTiter 96 AQueous One Solution Reagent contains a tetrazolium compound [3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, inner salt; MTS] and an electron coupling reagent (phenazine ethosulfate; PES). PES has enhanced chemical stability, which allows it to be combined with MTS to form a stable solution. The CellTiter 96 AQueous Assay uses phenazine methosulfate (PMS) as the electron coupling reagent, and PMS Solution and MTS Solution are supplied separately. PES has enhanced chemical stability, which allows it to be combined with MTS to form a stable solution. Assays are performed by adding a small amount of the CellTiter 96 AQueous One Solution Reagent directly to culture wells, incubating for 1-4 hours and then recording absorbance at 490nm with a 96-well plate reader. The quantity of formazan product as measured by the amount of 490nm absorbance is directly proportional to the number of living cells in culture. If you currently use a [(3)H]-thymidine incorporation assay, addition of the CellTiter 96 AQueous One Solution Reagent can be substituted for the pulse of [(3)H]-thymidine at the time point in the assay when the pulse of radioactive thymidine is usually added. Previous bioassay data comparing [(3)H]-thymidine incorporation to the MTS-based CellTiter 96 AQueous Assay and the original MTT-based CellTiter 96 Assay demonstrate that tetrazolium reagents can be substituted for [(3)H]-thymidine incorporation.
CellTiter-Blue® cell viability assay is based on living cells’ ability to convert a redox dye into a fluorescent end product. It can be used to monitor viability in adherent or non-adherent cells. CellTiter-Fluor® cell viability assay is a non-lytic, single-reagent-addition fluorescence that measures the number of viable cells in a population in as little as 30 minutes. The assay is based on measurement of a conserved and constitutive protease activity within living cells.
CellTiter-Glo™ luminescent cell viability assay involves the addition of one reagent directly to cells in culture for cell lysis and the generation of a luminescent signal proportional to the amount of ATP present. ATP is a marker of cell viability. The protocol allows for results in as little as 10 minutes using few cells per assay.
