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dc.creatorPark,Daniel J
dc.date2005-08-01
dc.date.accessioned2019-05-03T12:44:13Z
dc.date.available2019-05-03T12:44:13Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0717-34582005000200012
dc.identifier.urihttp://revistaschilenas.uchile.cl/handle/2250/84827
dc.descriptionThe determination of genomic DNA sequence flanking a known region is often problematic. Existing technologies depend on multiple, efficient enzyme-catalysed preparative processing steps and/or rely on relatively inefficient one-sided' PCR mechanisms. I demonstrate the application of a simple two-sided' PCR-based approach, lariat-dependent nested PCR for rapid amplification of genomic DNA ends (LaNe RAGE), applied to the mouse GAPDH and PGK1 gene flanking sequences. This demonstration offers great promise in applications such as genome walking, transposon mutagenesis mapping and DNA fingerprinting
dc.formattext/html
dc.languageen
dc.publisherPontificia Universidad Católica de Valparaíso
dc.relation10.4067/S0717-34582005000200012
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceElectronic Journal of Biotechnology v.8 n.2 2005
dc.subjectcloning
dc.subjectDNA fingerprinting
dc.subjectgenomic DNA walking
dc.subjectPCR
dc.subjectsequencing
dc.subjecttransposon mutagenesis
dc.titleLaNe RAGE: a new tool for genomic DNA flanking sequence determination


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