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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1982-8-26
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pubmed:abstractText |
The construction of a plasmid vector which facilitates the cloning and recovery of blunt-ended DNA fragments is described. This plasmid, called pHP34, differs from pBR322 by a 10-bp insertion which introduces a unique SmaI site immediately flanked by two EcoRI sites. Blunt-ended DNA fragments cloned in the SmaI site can be recovered by digestion with EcoRI. Small cloned fragments can be chemically sequenced using a strategy which does not require their purification. The use of a plasmid related to pHP34 for in vitro mutagenesis by the insertion of a DNA linker fragment conferring an antibiotic resistance is also discussed.
|
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
0378-1119
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
17
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
189-96
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:6282713-Base Sequence,
pubmed-meshheading:6282713-Cloning, Molecular,
pubmed-meshheading:6282713-DNA, Bacterial,
pubmed-meshheading:6282713-Escherichia coli,
pubmed-meshheading:6282713-Genetic Vectors,
pubmed-meshheading:6282713-Mutation,
pubmed-meshheading:6282713-Phenotype,
pubmed-meshheading:6282713-Plasmids,
pubmed-meshheading:6282713-Recombination, Genetic
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pubmed:year |
1982
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pubmed:articleTitle |
A modified pBR322 vector with improved properties for the cloning, recovery, and sequencing of blunt-ended DNA fragments.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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