Protocol tips
Upstream tips |
Protocol tips |
Downstream tips |
This kit uses a green fluorescent probe that reacts with autophagic vacuoles and is detectable by flow cytometry |
Incubate cells with CYTO-ID dye (2μl of CYTO-ID in 1ml of 1X assay buffer) for 30 min |
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 |
Incubate cells with CYTO-ID dye (2μl of CYTO-ID in 1ml of 1X assay buffer) for 30 min |
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 |
Publication protocol
Cyto-ID Autophagy Detection Kit (Enzo Life Sciences, ENZ-51031) was used to stain live cells according to manufacturer’s instructions. This assay is dependent on a 488 nm-excitable green fluorescent detection reagent which specifically fluoresces in autophagic vesicles. An increase in the 488-2A channel represents an increase in the number of autophagic vesicles staining green.
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Papers
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Paper title
MiR-193b promotes autophagy and non-apoptotic cell death in oesophageal cancer cells
Manufacturer protocol
Download the product protocol from Enzo Life Sciences for CYTO-ID® Autophagy detection kit below.
Download manufacturer protocol
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