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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1995-1-17
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pubmed:abstractText |
We have developed a simple PCR based approach for synthesizing high-molecular-weight DNA multimers of short oligonucleotide elements in yields sufficient for preparing DNA affinity columns or for using as probes to detect sequence-specific DNA binding proteins. The technique is rapid, efficient and produces multimers consisting of 30-100 repeating units.
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pubmed:grant | |
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 |
Nov
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pubmed:issn |
0006-291X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
30
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pubmed:volume |
205
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
475-81
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:7999067-Base Sequence,
pubmed-meshheading:7999067-Biopolymers,
pubmed-meshheading:7999067-Chromatography, Affinity,
pubmed-meshheading:7999067-DNA,
pubmed-meshheading:7999067-Electrophoresis, Agar Gel,
pubmed-meshheading:7999067-Molecular Sequence Data,
pubmed-meshheading:7999067-Molecular Weight,
pubmed-meshheading:7999067-Polymerase Chain Reaction
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pubmed:year |
1994
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pubmed:articleTitle |
A rapid and efficient PCR-based method for synthesizing high-molecular-weight multimers of oligonucleotides.
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pubmed:affiliation |
Laboratory of Structural Biology and Molecular Medicine, UCLA School of Medicine 90024.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.
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