| Literature DB >> 18265117 |
P R Mueller1, B Wold, P A Garrity.
Abstract
This unit describes how PCR can be used to exponentially amplify segments of DNA located between two specified primer hybridization sites. A single-sided PCR method is used that initially requires specification of only one primer hybridization site; the second is defined by the ligation-based addition of a unique DNA linker. This linker, together with the flanking gene-specific primer, allows exponential amplification of any fragment of DNA. Because a defined, discrete-length sequence is added to every fragment, complex populations of DNA such as sequence ladders can be amplified intact with retention of single-base resolution. The ligation-based protocol was specifically designed for genomic footprinting and direct sequencing reactions, and is described in this context; it can, however, be used for other applications.Mesh:
Substances:
Year: 2001 PMID: 18265117 DOI: 10.1002/0471142727.mb1503s56
Source DB: PubMed Journal: Curr Protoc Mol Biol ISSN: 1934-3647