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Found 3 matching solutions for this experiment
Upstream tips |
Protocol tips |
Downstream tips |
|
To yield high RNA, give the column an extra wash with both RW1 and RPE buffers (3 total washes with each buffer). |
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 |
Protocol tips |
To yield high RNA, give the column an extra wash with both RW1 and RPE buffers (3 total washes with each buffer). |
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 |
|
For low 260/230 readings the best approach is to try washing sample (precipitation) with ethanol to desalt it. |
|
Protocol tips |
For low 260/230 readings the best approach is to try washing sample (precipitation) with ethanol to desalt it. |
TRIzol Reagent + QIAquick PCR Purification Kit
Upstream tips |
Protocol tips |
Downstream tips |
|
For low 260/230 readings the best approach is to try washing sample (precipitation) with ethanol to desalt it. |
|
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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