A single-tube assembly of DNA using the transfer-PCR (TPCR) platform
Methods in Molecular Biology, ISSN: 1064-3745, Vol: 1116, Page: 89-101
2014
- 22Citations
- 40Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations22
- Citation Indexes22
- 22
- CrossRef16
- Captures40
- Readers40
- 40
Book Chapter Description
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. © Springer Science+Business Media New York 2014.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84903363802&origin=inward; http://dx.doi.org/10.1007/978-1-62703-764-8_7; http://www.ncbi.nlm.nih.gov/pubmed/24395359; https://link.springer.com/10.1007/978-1-62703-764-8_7; https://dx.doi.org/10.1007/978-1-62703-764-8_7; https://link.springer.com/protocol/10.1007/978-1-62703-764-8_7
Springer Science and Business Media LLC
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