The CellTox™ Green Cytotoxicity Assay measures changes in membrane integrity that occur as a result of cell death. The assay is intended to assess cytotoxicity in cell culture after experimental manipulation. The assay system uses a proprietry asymmetric cyanine dye that is excluded from viable cells but preferentially stains the DNA from dead cells. When the dye binds DNA released from cells, its fluorescence properties are substantially enhanced. Viable cells produce no appreciable increases in fluorescence. Therefore, the fluorescence signal produced by the binding interaction with dead cell DNA is propo...
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The CellTox™ Green Cytotoxicity Assay measures changes in membrane integrity that occur as a result of cell death. The assay is intended to assess cytotoxicity in cell culture after experimental manipulation. The assay system uses a proprietry asymmetric cyanine dye that is excluded from viable cells but preferentially stains the DNA from dead cells. When the dye binds DNA released from cells, its fluorescence properties are substantially enhanced. Viable cells produce no appreciable increases in fluorescence. Therefore, the fluorescence signal produced by the binding interaction with dead cell DNA is proportional to cytotoxicity. The CellTox™ Green Dye is non-toxic to cells, and the signal remains constant after exposure of 72 hours, making it ideal for determining toxic effects of treatments throughout an extended exposure or as an endpoint determination.
Determine cytotoxic effects of treatments on cells in culture after long-term exposure.
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CellTox™ Green Cytotoxicity Assay
Lysis Solution
Assay Buffer
CellTox™ Green Dye, 1,000X
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CellTox™ Green Express Cytotoxicity Assay
Store at –20°C.
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Staurosporine was applied to K562 cells after introducing the CellTox™ Green Dye following the Express, No-Step Addition Method at Seeding Protocol. Fluorescence associated with the progression of cytotoxicity was measured after 24, 48 and 72 hours of cell exposure.
CellTox™ Green Reagent was applied to bortezomib-treated K562 cells after 48 hours of exposure. Fluorescence associated with cytotoxicity was measured, then CellTiter-Glo® Reagent applied and bioluminescence associated with viability measured. These inverse measures produce similar EC50 values.
G8741, G8742, G8743, G8731 For Research Use Only. Not for Use in Diagnostic Procedures.
Patent Pending.
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