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Found 3 matching solutions for this experiment
Upstream tips |
Protocol tips |
Downstream tips |
- This kit can be used for the isolation of RNA from up to 5x10^5 cells, or up to 5 mg of tissue. |
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- Always blank the spectrophotometer with your elution buffer.
- When measuring 260 nm absorbance, a unit of 1 on this scale equals to 40 ng of RNA. |
Upstream tips |
- This kit can be used for the isolation of RNA from up to 5x10^5 cells, or up to 5 mg of tissue. |
Downstream tips |
- Always blank the spectrophotometer with your elution buffer.
- When measuring 260 nm absorbance, a unit of 1 on this scale equals to 40 ng of RNA. |
Upstream tips |
Protocol tips |
Downstream tips |
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- Include DNAse treatment for 15-20min.
- Ensure EtOH is completely evaporated off of the column prior to elution. Adjust time from 1min to 5 min at 60`C.
- Use water to elute the RNA that is warmed to ~60`C.
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Downstream tips |
- Include DNAse treatment for 15-20min.
- Ensure EtOH is completely evaporated off of the column prior to elution. Adjust time from 1min to 5 min at 60`C.
- Use water to elute the RNA that is warmed to ~60`C.
|
Upstream tips |
Protocol tips |
Downstream tips |
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- For low 260/230 readings the best approach is to try washing sample (precipitation) with ethanol to desalt it. |
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Protocol tips |
- For low 260/230 readings the best approach is to try washing sample (precipitation) with ethanol to desalt it. |
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