Title |
pPCV, a versatile vector for cloning PCR products
|
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Published in |
SpringerPlus, September 2013
|
DOI | 10.1186/2193-1801-2-441 |
Pubmed ID | |
Authors |
Christiane R Janner, Ana Lívia P Brito, Lidia Maria P Moraes, Viviane CB Reis, Fernando AG Torres |
Abstract |
The efficiency of PCR product cloning depends on the nature of the DNA polymerase employed because amplicons may have blunt-ends or 3' adenosines overhangs. Therefore, for amplicon cloning, available commercial vectors are either blunt-ended or have a single 3' overhanging thymidine. The aim of this work was to offer in a single vector the ability to clone both types of PCR products. For that purpose, a minimal polylinker was designed to include restriction sites for EcoRV and XcmI which enable direct cloning of amplicons bearing blunt-ends or A-overhangs, respectively, still offering blue/white selection. When tested, the resulting vector, pPCV, presented high efficiency cloning of both types of amplicons. |
Mendeley readers
Geographical breakdown
Country | Count | As % |
---|---|---|
Unknown | 14 | 100% |
Demographic breakdown
Readers by professional status | Count | As % |
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Student > Master | 6 | 43% |
Student > Ph. D. Student | 2 | 14% |
Researcher | 2 | 14% |
Student > Bachelor | 1 | 7% |
Professor > Associate Professor | 1 | 7% |
Other | 0 | 0% |
Unknown | 2 | 14% |
Readers by discipline | Count | As % |
---|---|---|
Agricultural and Biological Sciences | 7 | 50% |
Biochemistry, Genetics and Molecular Biology | 4 | 29% |
Immunology and Microbiology | 1 | 7% |
Unknown | 2 | 14% |