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Thread | Thread Starter | Forum | Replies | Last Post |
Help with denaturing low concentration Illumina PE Library | TonyBrooks | Sample Prep / Library Generation | 3 | 09-27-2010 09:30 AM |
Better to risk low concentration library or further amplification? | krobison | Sample Prep / Library Generation | 3 | 08-12-2010 02:40 PM |
Low concentration GA library | Melanie | Sample Prep / Library Generation | 4 | 08-04-2010 02:34 PM |
low cDNA concentration after the RAPID protocol | dina | 454 Pyrosequencing | 0 | 07-11-2010 12:48 PM |
Anyone use low concentration for ChIP-seq prep? | Audry888 | Sample Prep / Library Generation | 4 | 05-28-2010 12:37 PM |
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#1 |
Member
Location: New York Join Date: Mar 2011
Posts: 26
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Hi Friends
I am using TruSeq whole RNA sequencing kit. I used 50 ng input of earlier purified mRNA and gave a 15 cycle. At the end, the libraries were dissolved in 30 microliter of RSB buffer. Out of 4 libraries, one of the library is 1/10 of others in terms of concentration of dsDNA. Should I be worried? I have not yet done any bioanalyzer analysis. Biochembug |
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