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Found 4 matching solutions for this experiment
Upstream tips |
Protocol tips |
Downstream tips |
- 0.5-1 × 10^6 cells were cultured in a 6 welll plate
- cells were pretreated with absence or presence of AZD8055 (500 nM).
- Radiation was applied 4 h later. |
- Annexin V and PI are added and incubated for 15 min at RT in the dark |
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Upstream tips |
- 0.5-1 × 10^6 cells were cultured in a 6 welll plate
- cells were pretreated with absence or presence of AZD8055 (500 nM).
- Radiation was applied 4 h later. |
Protocol tips |
- Annexin V and PI are added and incubated for 15 min at RT in the dark |
Upstream tips |
Protocol tips |
Downstream tips |
- Cells were pre treated with 8 μM sorafenib for 24h.
- 1 × 10^6 cells were used for the assay. |
- Add FITC Annexin V and 7-AAD Viability Staining Solution and incubate for 15 min at RT. |
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Upstream tips |
- Cells were pre treated with 8 μM sorafenib for 24h.
- 1 × 10^6 cells were used for the assay. |
Protocol tips |
- Add FITC Annexin V and 7-AAD Viability Staining Solution and incubate for 15 min at RT. |
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- Cells were treated with 1 μM 3-Cl-AHPC and AHP3 for various indicated time. |
- Treated with FITC Annexin V and PI and incubated for 15 min at RT (25°C) in the dark |
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Upstream tips |
- Cells were treated with 1 μM 3-Cl-AHPC and AHP3 for various indicated time. |
Protocol tips |
- Treated with FITC Annexin V and PI and incubated for 15 min at RT (25°C) in the dark |
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- Cells were incubated with ice-cold 70% ethanol overnight
at −20 °C.
- Cells were incubated for 1 h at 36 °C after treated with DNA-labeling solution |
|
Protocol tips |
- Cells were incubated with ice-cold 70% ethanol overnight
at −20 °C.
- Cells were incubated for 1 h at 36 °C after treated with DNA-labeling solution |
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