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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1992-3-12
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pubmed:abstractText |
This report presents data demonstrating a simple method that can potentially be extended to a wide range of cloning strategies to increase the yield of insert-containing recombinants. The method requires that the ligation of an insert to a vector does not regenerate the original restriction enzyme recognition sequence. In the example presented, PCR products were blunt-end ligated to a SmaI-cut vector, in the presence of SmaI endonuclease. The addition of the restriction enzyme to the ligation reaction dramatically favored the ligation of insert to vector rather than vector self-ligation.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0736-6205
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
12
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
28, 30
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pubmed:dateRevised |
2008-8-29
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pubmed:meshHeading |
pubmed-meshheading:1734919-Cloning, Molecular,
pubmed-meshheading:1734919-DNA,
pubmed-meshheading:1734919-Deoxyribonucleases, Type II Site-Specific,
pubmed-meshheading:1734919-Escherichia coli,
pubmed-meshheading:1734919-Genetic Vectors,
pubmed-meshheading:1734919-Plasmids,
pubmed-meshheading:1734919-Polymerase Chain Reaction,
pubmed-meshheading:1734919-Transformation, Bacterial
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pubmed:year |
1992
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pubmed:articleTitle |
An efficient method for blunt-end ligation of PCR products.
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pubmed:affiliation |
Molecular and Cellular Biology Program, Morrill Science Center, University of Massachusetts, Amherst 01003.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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