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Found 3 matching solutions for this experiment
Upstream tips |
Protocol tips |
Downstream tips |
- Cells were treated with or without 5, 10 and 20 μM of HMJ-30 for 24 h |
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- Non specific labelling can be corrected by fixing cells by treating with 4% buffer PFA or Formalin.
- When Nonspecific labelling is present, reduce concentration of TdT
- When high background is present reduce concentration of labelling mix by 50% |
Upstream tips |
- Cells were treated with or without 5, 10 and 20 μM of HMJ-30 for 24 h |
Downstream tips |
- Non specific labelling can be corrected by fixing cells by treating with 4% buffer PFA or Formalin.
- When Nonspecific labelling is present, reduce concentration of TdT
- When high background is present reduce concentration of labelling mix by 50% |
Upstream tips |
Protocol tips |
Downstream tips |
- Cells were cultured in 35 mm2 disks |
- After treating cells with Annexin V and PI working solution they are incubated with Annexin-binding buffer on ice |
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Upstream tips |
- Cells were cultured in 35 mm2 disks |
Protocol tips |
- After treating cells with Annexin V and PI working solution they are incubated with Annexin-binding buffer on ice |
Upstream tips |
Protocol tips |
Downstream tips |
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- Treated with FITC Annexin V and PI and incubated for 15 min at RT (25°C) in the dark |
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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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