| Literature DB >> 10769760 |
Abstract
The isolation of a single DNA molecule for cloning is technically difficult, and the subsequent screening of colonies for recombinant DNA clones is time consuming. Ion pair-reversed phase HPLC (IP-RP-HPLC) analysis of nucleic acids improves the resolution and isolation of PCR products to be cloned. We demonstrate that PCR products analyzed and collected using the IP-RP-HPLC approach (WAVE DNA Fragment Analysis System) can be cloned directly into a plasmid vector. In addition, we demonstrate that when IP-RP-HPLC analysis is extended to the colony screening process, the time required for these procedures is reduced.Entities:
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Year: 2000 PMID: 10769760 DOI: 10.2144/00284pf02
Source DB: PubMed Journal: Biotechniques ISSN: 0736-6205 Impact factor: 1.993