Protocol tips
Upstream tips |
Protocol tips |
Downstream tips |
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Stain the cells with Cyto-ID dye for 15min at 37°C |
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Protocol tips |
Stain the cells with Cyto-ID dye for 15min at 37°C |
Publication protocol
U87MG and U251MG cells were seeded in cell culture dishes with glass bottoms (NEST Biotechnology, Jiangsu Province, China), then treated with or without asparaginase (1 IU/mL) for 48 h after complete attachment. Cells treated with autophagy inducer rapamycin (50 mM) for 2 h were served as positive controls. Subsequently, cells were stained with Cyto-ID® Green dye and Hoechst 33342 for 15 min at 37°C and observed using a confocal microscope (Carl Zeiss LSM710, Carl Zeiss, Germany). All the steps were performed in the dark.
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Autophagy suppression potentiates the anti-glioblastoma effect of asparaginase and
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