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Cell Proliferation and Viability Measurement

WST-1 was added, and the cells were reincubated for another 2 hours. Then, the formazan product was quantified at 450 nm with an absorbance reader (Figure 3). Subsequently, BrdU incorporation was determined using the Cell Proliferation ELISA, BrdU (colorimetric). The results show that Actinomycin D inhibits DNA synthesis, but it does not inhibit the metabolic activity of the cell. Thus, actinomycin D is cytostatic (inhibits DNA synthesis) but not cytotoxic (no inhibition of metabolic activity).



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Related biology technology :

1. Cell Proliferation Kit Outperforms the Competition in the Range of Cells Typically Counted
2. Quantitative Measurement of Cell Proliferation Using the BrdU ELISA: A Comparison Between Colorimetric and Chemiluminescent Detection
3. measuring cell proliferation with SpectraMax M5, M2 and Gemini microplate readers using the CyQUANT Cell Proliferation Assay
4. Cell Proliferation Assay Using the Benchmark Plus Microplate Spectrophotometer
5. Identification of cells in S phase using the Cell Proliferation Fluorescence Kit and IN Cell Analyzer 1000
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7. LIVE/DEAD Viability/Cytotoxicity Assay for Animal Cells Using the SpectraMax Gemini XS Fluorescence Microplate Reader (MaxLine Application Note #43)
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10. LabVIEW for Measurement and Data Analysis
11. Use of FlashPlate Technology for In Vitro Measurement of [35S]-GTPγS Binding in CHO Cells Expressing the Human 5-HT1B Receptor
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