Protocol tips
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" |
Publication protocol
Samples taken in the exponential growth phase were employed for RNA isolation using the RNeasy Mini Kit (Qiagen, Hilden, Germany), with both an on- and off-column gDNA digestion step. RNA quantity and the absence of gDNA and other contaminants was assayed with the DropSense16 system (Trinean, Ghent, Belgium).
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Paper title
Non-canonical integration events in encountered during standard transformation analysed with genome sequencing
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