Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
|
pubmed:dateCreated |
1992-12-10
|
pubmed:abstractText |
A procedure utilizing immobilized DNase I that allows the efficient amplification of cDNA by PCR from a single cell in the absence of contaminating genomic DNA is described. DNase I treated, total RNA derived from single cells was reverse transcribed into cDNA followed by PCR using beta-actin and c-fos specific primers that recognize different exons of the respective genes. Amplification products corresponding to cDNA, but not to genomic sequences, were detected after treatment with immobilized DNase I in samples previously shown to be contaminated with genomic DNA. This method allows the efficient removal of DNA contaminating total RNA derived from a single cell.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
0736-6205
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
13
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
726-9
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:1418973-Artifacts,
pubmed-meshheading:1418973-Base Sequence,
pubmed-meshheading:1418973-DNA,
pubmed-meshheading:1418973-Deoxyribonuclease I,
pubmed-meshheading:1418973-Enzymes, Immobilized,
pubmed-meshheading:1418973-Molecular Sequence Data,
pubmed-meshheading:1418973-Polymerase Chain Reaction,
pubmed-meshheading:1418973-RNA, Messenger
|
pubmed:year |
1992
|
pubmed:articleTitle |
Single-cell cDNA-PCR: removal of contaminating genomic DNA from total RNA using immobilized DNase I.
|
pubmed:affiliation |
Dept. of Clinical Physiology & Occupational Medicine, University of Ulm, FRG.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|