Cell Counting Kit 8 / CCK-8 Assay Kit / WST-8 Assay Kit ab228554 is a no-wash, mix-and-read, cell viability assay. The ready-to-use solution is added to cell cultures for a 1-4 hour incubation, with a colorimetric (460 nm) readout proportional to the number of living cells.
- CCK-8 / WST-8 tetrazolium is reduced by cellular dehydrogenases in living cells and has very low cytotoxicity
- The CCK-8 assay has higher sensitivity than other tetrazolium salt-based assays, such as MTT, MTS or XTT
- Highly cited in >200 publications
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Cell Counting Kit 8 / CCK-8 Assay Kit / WST-8 Assay Kit ab228554 is a no-wash, mix-and-read, cell viability assay. The ready-to-use solution is added to cell cultures for a 1-4 hour incubation, with a colorimetric (460 nm) readout proportional to the number of living cells.
- CCK-8 / WST-8 tetrazolium is reduced by cellular dehydrogenases in living cells and has very low cytotoxicity
- The CCK-8 assay has higher sensitivity than other tetrazolium salt-based assays, such as MTT, MTS or XTT
- Highly cited in >200 publications
Cell Counting Kit 8 / CCK-8 Assay Kit / WST-8 Assay Kit ab228554 provides a convenient and robust way of performing a cell viability assay.
How the CCK-8 assay works
The CCK-8 assay uses a water-soluble tetrazolium salt to quantify the number of live cells by producing an orange formazan dye upon bio-reduction in the presence of an electron carrier. WST-8 solution is added directly to the test cells, no pre-mixing of components is required. WST-8 tetrazolium salt is reduced by cellular dehydrogenases to an orange formazan product that is soluble in tissue culture medium.
The amount of formazan produced is directly proportional to the number of living cells by monitoring absorbance increase at 460 nm. The excellent stability and little cytotoxicity of WST-8 solution make the kit useful for the assays that require long incubation (such as 24 to 48 hours).
CCK8 assay protocol summary
How other researchers are using CCK8 Kit ab228554
Cell Counting Kit 8 (WST-8 / CCK8) has been used in a variety of sample type including:
References: 1- Lin H et al. 2024; 2- Wu WC et al. 2023; 3- Wei D et al. 2023
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Cytotoxicity tests of HeLa cells in response to (A) SDS and (B) Staurosporine treatment were measured with The cell Counting Kit 8 (WST-8) (ab228554). HeLa cells at 10,000 cells/well/100 μL were seeded overnight in a black wall/clear bottom 96-well plate. Cells were treated with serially diluted SDS for 2 hours or Staurosporine for 4 hours. The absorbance was measured at 460 nm using a plate reader.
Cell Counting Assay.
Cell number was determined with the cell Counting Kit 8 (WST-8) (ab228554). (A) HeLa cells at 0 to 10,000 cells/well/100 μL, and (B) Jurkat cells at 0 to 100,000 cells/well/100 μL were added in a clear bottom 96-well plate. The absorbance was measured at 460 nm using a plate reader.
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