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Thread | Thread Starter | Forum | Replies | Last Post |
Size selection for TruSeq DNA libraries | anna_m | Sample Prep / Library Generation | 0 | 06-17-2013 06:54 AM |
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#1 |
Member
Location: France Join Date: May 2013
Posts: 24
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Dear all,
My samples quantities was 246, 184, 112, 133 and 232 ng. I pooled them all and run them in a gel for site selection. Afterward I did purified them using columns. Surprisingly and after ,measuring them with Qubit their quantity became 10.7 ng. First, I would like to know why they have such a low concentration? second, if the beads are the reason, then how can I avoid this? Third, will these samples still work to proceed with? for Ion one touch? |
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