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|Seed the cells in 8 well chamber slide to 30% confluency. After the appropriate treatment incubate with 100μl of dual detection reagent.|
|Incase of Low CYTO-ID Green dye staining in all treatments, increase the reagent concentration (500X dilution of the dye is recommended) and the incubation time.
Incase of High CYTO-ID Green staining, it could be that the cell culture medium was depleted of nutrients and so change media 4-8 hours before the experiment.