LaNe RAGE: a new tool for genomic DNA flanking sequence determination
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Keywords

cloning
DNA fingerprinting
genomic DNA walking
PCR
sequencing
transposon mutagenesis

How to Cite

1.
Park DJ. LaNe RAGE: a new tool for genomic DNA flanking sequence determination. Electron. J. Biotechnol. [Internet]. 2005 Aug. 15 [cited 2024 Oct. 13];8(2):0-. Available from: https://www.ejbiotechnology.info/index.php/ejbiotechnology/article/view/v8n2-7

Abstract

The 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.

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