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Thread | Thread Starter | Forum | Replies | Last Post |
Do we need the bioruptor? | SeqGeorge's | Ion Torrent | 5 | 08-11-2011 02:11 AM |
PCR product normalization | Palecomic | Sample Prep / Library Generation | 0 | 01-20-2011 02:50 AM |
Excess PCR primers in final product | PaulineF | Illumina/Solexa | 19 | 07-27-2010 05:23 AM |
Request for sequencing of PCR product | Damann | Core Facilities | 0 | 11-05-2009 08:34 AM |
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#1 |
Junior Member
Location: North Carolina Join Date: Apr 2012
Posts: 1
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We are pooling multiple PCR products that range in size from 700 to 2000 bp and would like to fragment them to approx. 450-500 bp before tagging them with barcodes.
Has anyone worked with PCR products vs. genomic DNA in a similar manner? We will be using a Bioruptor UCD-200. Thanks for your help! |
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#2 |
Junior Member
Location: Washington, D.C. Join Date: Nov 2013
Posts: 1
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Bernie,
I'm curious to know how your shearing worked for those mixed amplicon sizes. We are trying to develop a shearing protocol as well for amplicon pools of 300bp - 2kb. Thanks! |
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