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Found 3 matching solutions for this experiment
Upstream tips |
Protocol tips |
Downstream tips |
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- Cells were treated with different concentrations of 5‘-Cl (0.0 to 8.0 µM) for 24h or with 4.0 µM for various periods of time (0 to 48h).
- Cells were fixed in ice-cold 70% ethanol at -20°C for 3h.
- Stained with 200 µL of PI/RNAse reagent for 30 min. |
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Protocol tips |
- Cells were treated with different concentrations of 5‘-Cl (0.0 to 8.0 µM) for 24h or with 4.0 µM for various periods of time (0 to 48h).
- Cells were fixed in ice-cold 70% ethanol at -20°C for 3h.
- Stained with 200 µL of PI/RNAse reagent for 30 min. |
Upstream tips |
Protocol tips |
Downstream tips |
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- Cells were treated with 10 µM of 11, or 1 µM of colchicine as a control, for 20 h..
-After incubation cells were centrifuged twice (before (1000 rpm for 5 min) and after (3000 rpm for 5 min) washing. |
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Protocol tips |
- Cells were treated with 10 µM of 11, or 1 µM of colchicine as a control, for 20 h..
-After incubation cells were centrifuged twice (before (1000 rpm for 5 min) and after (3000 rpm for 5 min) washing. |
Upstream tips |
Protocol tips |
Downstream tips |
- Dilute
an appropriate amount of the antibody stock solution
1:50 with 1X BD Perm/Wash Buffer
- Store unused portions
of 1X BD Perm/Wash Buffer at 4°C. |
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|
Upstream tips |
- Dilute
an appropriate amount of the antibody stock solution
1:50 with 1X BD Perm/Wash Buffer
- Store unused portions
of 1X BD Perm/Wash Buffer at 4°C. |
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