A single-tube assembly of DNA using the transfer-PCR (TPCR) platform

Ariel Erijman, Julia M. Shifman, Yoav Peleg

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

19 Scopus citations

Abstract

DNA cloning is a basic methodology employed for multiple applications in all life-science disciplines. In order to facilitate DNA cloning we developed Transfer-PCR (TPCR), a novel approach that integrates in a single tube, PCR amplification of the target DNA from an origin vector and its subsequent integration into the destination vector. TPCR can be applied for incorporation of DNA fragments into any desired position within a circular plasmid without the need for purification of the intermediate PCR product and without the use of any commercial kit. TPCR reaction is most efficient within a narrow range of primer concentrations. Adaptation of the TPCR should facilitate, simplify, and significantly reduce time and costs for DNA assembly, as well as protein engineering studies. In the current publication we describe a detailed protocol for implementation of the TPCR method for DNA assembly.

Original languageAmerican English
Title of host publicationDNA Cloning and Assembly Methods
PublisherHumana Press Inc.
Pages89-101
Number of pages13
ISBN (Print)9781627037631
DOIs
StatePublished - 2014

Publication series

NameMethods in Molecular Biology
Volume1116
ISSN (Print)1064-3745

Keywords

  • DNA cloning
  • Ligation-Independent Cloning (LIC)
  • Restriction-Free (RF) cloning
  • Transfer-PCR (TPCR)

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