MTT Cell Viability Assay Kit (1000 Assays)
Référence 30006
Conditionnement : 1kit
Marque : Biotium
MTT Cell Viability Assay Kit
A simple, colorimetric assay for determining live cell numbers by absorbance on a microplate reader.
Product Description
The MTT Cell Viability Assay Kit provides a simple method for determining live cell numbers by absorbance on a microplate reader. MTT is a tetrazolium salt that is turned into a purple formazan product after reduction by mitochondrial enzymes that are only present in metabolically active live cells. The amount of formazan product generated is proportional to the number of living cells in the sample.
- Measure cell metabolism by reading absorbance at 570 nm
- Non-radioactive, simple procedure
- Endpoint assay, requires cell lysis
Determination of live cell numbers is often used to assess the rate of cell proliferation and cytotoxicity caused by drugs and cytotoxic agents. Among all non-radioactive viability assays, MTT assay developed by Mossman is one of the most versatile and popular assays. At the end of the assay, the cells containing the formazan product are solubilized and then photometrically quantified at 570 nm.
Also see the XTT Cell Viability Assay Kit, which does not require solubilization before absorbance measurement.
Technology
Product Attributes
Size
Apoptosis/viability marker
For live or fixed cells
Assay type/options
Detection method/readout
Storage Conditions
Documents, Protocols, SDS and COA
Documents
COA
Request the Certificate of AnalysisReferences
1. PLoS ONE (2011) 6(8): e22635. doi:10.1371/journal.pone.0022635
2. Cell (2011) 145, 941-955. doi:10.1016/j.cell.2011.05.004
3. PLoS ONE (2012) 7(4): e35866. doi:10.1371/journal.pone.0035866
4. J. Virol (2013) Jul;87(14):8179-94. doi:10.1128/JVI.00443-13
5. J Am Chem Soc. (2014) Apr 9;136(14):5295-300. doi: 10.1021/ja408505n.
6. Endocrinology. (2015) Dec;156(12):4695-706. doi: 10.1210/en.2015-1500
7. J Mol Neurosci. (2015) May;56(1):122-30. doi: 10.1007/s12031-014-0473-6
8. Nat Commun (2016) Feb 16;7:10686. doi: 10.1038/ncomms10686
Citations
1. PLoS ONE (2011) 6(8): e22635. doi:10.1371/journal.pone.0022635
2. Cell (2011) 145, 941-955. doi:10.1016/j.cell.2011.05.004
3. PLoS ONE (2012) 7(4): e35866. doi:10.1371/journal.pone.0035866
4. J. Virol (2013) Jul;87(14):8179-94. doi:10.1128/JVI.00443-13
5. J Am Chem Soc. (2014) Apr 9;136(14):5295-300. doi: 10.1021/ja408505n.
6. Endocrinology. (2015) Dec;156(12):4695-706. doi: 10.1210/en.2015-1500
7. J Mol Neurosci. (2015) May;56(1):122-30. doi: 10.1007/s12031-014-0473-6
8. Nat Commun (2016) Feb 16;7:10686. doi: 10.1038/ncomms10686
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