6 results in 0.0030 seconds.
-
Ampure (Kapa pure) beads at -20
We mistakenly stored our Kapa pure beads at -20 for about 9 days. They were not frozen when we checked. Would they still be usable? Has anyone done this... -
Bead removal of <1000 bp from LARGE fragments
Hi,
Trying to prep some very large fragment libraries (>50 kbp), and I've isolated the gDNA using a BluePippin, but when I use beads... -
Getting rid of primer dimer for RNA-Seq libraries
Hey all, I just found several of my RNA-Seq libraries have primer dimers, I was wondering what is the ratio of my final product that is now diluted in... -
Illumina Sample Purification Beads vs AMPure XP Beads
I have left over SPB from my Illumina kits, would they be OK to use as a substitute for AMPure XP beads? Provided they're still in date -
127bp adaptor dimer
Hi all,
I ran Bioanalyser on the PCR products of my RNA-Seq library prep, and there are adaptor dimers contamination in all my samples.... -
evaluation of various size-selection procedures
Hi everybody
We are currently optimizing our DNA library prep workflow for downstream SOLiD sequencing and I am comparing the various possibilities...Last edited by DirkS; 03-29-2013, 03:20 AM.
