Hi
I am trying to use AMPure XP beads to size select miRNA libraries. I am following the NEB protocol and the recommended cut off is 1.3x and 3.7x for smaller and larger respectively. I was wondering if anyone has tried this before and if so how stringent is the selection? The figure from NEB protocol shows a peak only at 147 removing all other fragments. Does this mean that the protocol needs to be tweaked every time we expect small RNAs other than miRNA?
Thank you.
I am trying to use AMPure XP beads to size select miRNA libraries. I am following the NEB protocol and the recommended cut off is 1.3x and 3.7x for smaller and larger respectively. I was wondering if anyone has tried this before and if so how stringent is the selection? The figure from NEB protocol shows a peak only at 147 removing all other fragments. Does this mean that the protocol needs to be tweaked every time we expect small RNAs other than miRNA?
Thank you.