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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
|
| pubmed:dateCreated |
1985-9-19
|
| pubmed:abstractText |
We have used a plasmid which contains a cloned fragment of T7 DNA to study the properties of general recombination of phage T7 in vitro. It was shown that T7-infected cell extracts promote recombination by the exchange of double strands of DNA. While both products of these double-strand exchanges were detected, we were unable to show that they were formed during a single recombination event.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Apr
|
| pubmed:issn |
0714-7511
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
63
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
243-8
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:2990644-Cloning, Molecular,
pubmed-meshheading:2990644-DNA, Recombinant,
pubmed-meshheading:2990644-DNA, Viral,
pubmed-meshheading:2990644-DNA Restriction Enzymes,
pubmed-meshheading:2990644-Escherichia coli,
pubmed-meshheading:2990644-Plasmids,
pubmed-meshheading:2990644-Recombination, Genetic,
pubmed-meshheading:2990644-T-Phages
|
| pubmed:year |
1985
|
| pubmed:articleTitle |
In vitro recombination of bacteriophage T7 DNA: further characterization of the reaction using plasmid DNA.
|
| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|