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MTS Cell Proliferation Assay

Published by mike.cellassay, 2022-02-06 16:10:28

Description: MTS cell proliferation assay is a colorimetric and high throughput method for sensitive quantification of viable cells, which is performed by adding the reagent into the cell culture media without the intermittent steps and requires no washing or solubilization step. The NAD(P)H-dependent dehydrogenase enzymes in metabolically active cells can cause the reduction of the MTS tetrazolium compound and generate the colored formazan product that is soluble in cell culture media. Since viable cells can convert the MTS tetrazolium compound to the soluble and colored formazan product, color intensity can be significantly increased by measuring absorbance at 490-500 nm.

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MTS Cell Proliferation Assay MTS cell proliferation assay is a colorimetric and high throughput method for sensitive quantification of viable cells, which is performed by adding the reagent into the cell culture media without the intermittent steps and requires no washing or solubilization step. The NAD(P)H- dependent dehydrogenase enzymes in metabolically active cells can cause the reduction of MTS tetrazolium compound and generate the colored formazan product that is soluble in cell culture media. Since viable cells can convert the MTS tetrazolium compound to the soluble and colored formazan product, color intensity can be significantly increased by measuring absorbance at 490- 500 nm. Overview of MTS Cell Proliferation Assay Service At Creative Bioarray, we provide MTS cell proliferation assay for the sensitive quantification of viable cells. The MTS cell proliferation assay involves culturing and treating cells, as well as adding MTS directly to the assay wells at a recommended ratio. Cells are incubated 1-4 hours and then absorbance is measured. MTS cell proliferation assay procedure At Creative Bioarray, we can apply our MTS cell proliferation assay to various fields, including but not limited: • Measurement of cell proliferation in response to growth factors, cytokines, mitogens and nutrients. • Analysis of cytotoxic and cytostatic compounds, such as anticancer drugs and pharmaceutical compounds. • Assessment of physiological mediators that inhibit cell growth.


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