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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1988-5-24
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pubmed:abstractText |
We describe the construction and utilization of a new mobilizable cosmid vector. Using this vector, mobilizable libraries of bacterial DNA can be efficiently made without a need for size fractionation of target DNA. The low stability of this vector in Pseudomonas fluorescens makes it useful in a rapid strategy, which is not dependent on plasmid incompatibility, for recombining transposon-induced mutations into the bacterial chromosome.
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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:issn |
0378-1119
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
61
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
299-306
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pubmed:dateRevised |
2006-5-1
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pubmed:meshHeading |
pubmed-meshheading:2833429-Cosmids,
pubmed-meshheading:2833429-DNA,
pubmed-meshheading:2833429-DNA, Recombinant,
pubmed-meshheading:2833429-DNA Transposable Elements,
pubmed-meshheading:2833429-Genetic Markers,
pubmed-meshheading:2833429-Immunochemistry,
pubmed-meshheading:2833429-Mutation,
pubmed-meshheading:2833429-Plasmids,
pubmed-meshheading:2833429-Pseudomonas fluorescens
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pubmed:year |
1987
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pubmed:articleTitle |
An efficient mobilizable cosmid vector, pRK7813, and its use in a rapid method for marker exchange in Pseudomonas fluorescens strain HV37a.
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pubmed:affiliation |
Advanced Genetic Sciences Inc., Oakland, CA 94608.
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pubmed:publicationType |
Journal Article
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