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Found 3 matching solutions for this experiment
Upstream tips |
Protocol tips |
Downstream tips |
- 3 × 10^4 were seeded in 96 well plate. |
- Cells were cultured in culture medium with and without fresh medium containing 5% FBS (as control) or 5% ascite in presence or not of H2O2 for 6 hours before adding APOPercentage Dye. |
- Wells were shaken for 20 minutes before being read at 540 nm |
Upstream tips |
- 3 × 10^4 were seeded in 96 well plate. |
Protocol tips |
- Cells were cultured in culture medium with and without fresh medium containing 5% FBS (as control) or 5% ascite in presence or not of H2O2 for 6 hours before adding APOPercentage Dye. |
Downstream tips |
- Wells were shaken for 20 minutes before being read at 540 nm |
Upstream tips |
Protocol tips |
Downstream tips |
- Cells were pre treated with artonin E at different time points |
- Cells were Dounce-homogenized before centrifuging at 7,000×g for 10 min at 4°C. |
|
Upstream tips |
- Cells were pre treated with artonin E at different time points |
Protocol tips |
- Cells were Dounce-homogenized before centrifuging at 7,000×g for 10 min at 4°C. |
Upstream tips |
Protocol tips |
Downstream tips |
- Do not freeze components |
- Add FITC Annexin V and 7-AAD Viability Staining Solution and incubate for 15 min at RT. |
|
Upstream tips |
- Do not freeze components |
Protocol tips |
- Add FITC Annexin V and 7-AAD Viability Staining Solution and incubate for 15 min at RT. |
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