CellTox Green Cytotoxicity Assay, Promega

Supplier: Promega Corporation

G8743 G8731 G8741 G8742
PAG8743EA 976.62 USD
PAG8743 PAG8731 PAG8741 PA-G8742
CellTox Green Cytotoxicity Assay, Promega
Assays Cellular Assays

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.


  • Real-Time Cytotoxicity Detection Assay With Multiplexing Compatibility
  • Accurate cytotoxicity determination in exposures out to 72 hours
  • Flexible protocol allows kinetic analysis or endpoint determination
  • Multiplex with luminescent assays to obtain more data per well


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 proprietary 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.


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.


The assay system uses a proprietary 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 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.

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