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Found 2 matching solutions for this experiment
Upstream tips |
Protocol tips |
Downstream tips |
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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. |
Protocol tips |
Seed the cells in 8 well chamber slide to 30% confluency. After the appropriate treatment incubate with 100μl of dual detection reagent. |
Downstream tips |
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. |
Upstream tips |
Protocol tips |
Downstream tips |
|
-Add primary Ab and incubate with agitation for 1 hour. |
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Protocol tips |
-Add primary Ab and incubate with agitation for 1 hour. |
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