Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
|
pubmed:dateCreated |
1997-4-17
|
pubmed:abstractText |
A pair of oligomers of 20 and 23 bp were designed for amplifying a 381 bp sequence from glycoprotein IV gene of bovine herpesvirus 1. The primer pairs were used for amplifying genomic DNA of BHV-1 directly from cell culture fluids under different experimental conditions such as, untreated cell culture fluid, thermal denaturation and proteinase K treatment in presence of detergent. The results reveal that direct thermal denaturation of cell culture fluid is sufficient to detect the virus by polymerase chain reaction.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
0019-5189
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
34
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1169-71
|
pubmed:dateRevised |
2004-2-9
|
pubmed:meshHeading |
pubmed-meshheading:9055637-Animals,
pubmed-meshheading:9055637-Base Sequence,
pubmed-meshheading:9055637-Cattle,
pubmed-meshheading:9055637-Cattle Diseases,
pubmed-meshheading:9055637-DNA, Viral,
pubmed-meshheading:9055637-DNA Primers,
pubmed-meshheading:9055637-Herpesviridae Infections,
pubmed-meshheading:9055637-Herpesvirus 1, Bovine,
pubmed-meshheading:9055637-Polymerase Chain Reaction,
pubmed-meshheading:9055637-Viral Proteins
|
pubmed:year |
1996
|
pubmed:articleTitle |
Direct detection of bovine herpes virus-1 DNA from cell culture fluids using polymerase chain reaction.
|
pubmed:affiliation |
Indian Veterinary Research Institute, Bangalore, India.
|
pubmed:publicationType |
Journal Article
|