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 |
- 2 µL of CYTO-ID® Green Detection Reagent and 1 µL of Hoechst 33342 Nuclear Stain for every 1 mL of 1X Assay Buffer or complete cell growth medium |
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 |
- 2 µL of CYTO-ID® Green Detection Reagent and 1 µL of Hoechst 33342 Nuclear Stain for every 1 mL of 1X Assay Buffer or complete cell growth medium |
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
Both control and GMs macrophages were cultured in chamber slides. After the different treatments, cells were washed twice with 1X assay buffer and stained using a Cyto‐ID Autophagy Detection Kit (Enzo life science, Farmingdale, NY, USA), according to the manufacturer's instructions. Cells were imaged by confocal microscopy using a 40X oil DIC objective.
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Papers
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Paper title
Lysosomal storage and impaired autophagy lead to inflammasome activation in aucher macrophages
Manufacturer protocol
Download the product protocol from Enzo Life Sciences for CYTO-ID® Autophagy detection kit below.
Download manufacturer protocol
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