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Found 2 matching solutions for this experiment
Upstream tips |
Protocol tips |
Downstream tips |
This kit uses a green fluorescent probe that reacts with autophagic vacuoles and is detectable by flow cytometry |
Use Cyto-ID green dye (1 μl/4 ml assay buffer) for 30 minutes in dark at RT. |
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 |
This kit uses a green fluorescent probe that reacts with autophagic vacuoles and is detectable by flow cytometry |
Protocol tips |
Use Cyto-ID green dye (1 μl/4 ml assay buffer) for 30 minutes in dark at RT. |
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 |
|
Stain the cells with CYTO-ID for 30 min at 37°C in the dark |
|
Protocol tips |
Stain the cells with CYTO-ID for 30 min at 37°C in the dark |
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