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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1991-4-23
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pubmed:abstractText |
We report an efficient procedure to synthesize either single- or double-stranded probes labeled with biotin-11-dUTP, biotin-21-dUTP or digoxigenin-11-dUTP. To produce the single-stranded probe, only a single primer is utilized in a Taq polymerase amplification of 55 cycles. A cytomegalovirus probe is presented. This procedure allows easy production of nonradioactively labeled pure single-stranded probes of any desired length and specificity.
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pubmed:grant | |
pubmed:commentsCorrections | |
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 |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
35-6, 38-9
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:2003918-Base Sequence,
pubmed-meshheading:2003918-DNA, Single-Stranded,
pubmed-meshheading:2003918-DNA Probes,
pubmed-meshheading:2003918-DNA-Directed DNA Polymerase,
pubmed-meshheading:2003918-Molecular Sequence Data,
pubmed-meshheading:2003918-Polymerase Chain Reaction,
pubmed-meshheading:2003918-Taq Polymerase
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pubmed:year |
1991
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pubmed:articleTitle |
Producing single-stranded DNA probes with the Taq DNA polymerase: a high yield protocol.
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pubmed:affiliation |
Fred Hutchinson Cancer Research Center, Seattle, WA 98104.
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pubmed:publicationType |
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't,
Technical Report
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