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
The cells were then grown at 30°C at 250 rpm for 6 h, 5 × 107 cells were harvested and washed, and RNA was extracted with a Qiagen RNeasy minikit (Qiagen, Hilden, Germany). For the analysis of glucose repression, myristic acid and glucose were added at a final concentration of 1% each.
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Papers
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Paper title
Defects in Mitochondrial and Peroxisomal β-Oxidation Influence Virulence in the Maize Pathogen
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