Source:http://linkedlifedata.com/resource/pubmed/id/19678569
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2009-8-14
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pubmed:abstractText |
A rapid detection of foot-and-mouth disease virus (FMDV) was established by using reverse transcription loop-mediated isothermal amplification (RT-LAMP) method, meanwhile its specificity and sensitivity were assessed. The results showed that the FMDV RNA could be amplified by incubation at 65degrees C for only 1h using six primers designed based on FMDV polyprotein gene and the amplification products could be detected easily by naked-eye. There is no cross reaction with other virus such as SVDV, SFV and PPV by detecting their RNA samples. The detection limit of this method was found to be 10(-5) dilution of RNA sample which was 100-fold higher than that of PCR and 10-fold higher than real-time PCR.
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pubmed:language |
chi
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1000-8721
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
25
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
137-42
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pubmed:meshHeading |
pubmed-meshheading:19678569-Animals,
pubmed-meshheading:19678569-DNA Primers,
pubmed-meshheading:19678569-Foot-and-Mouth Disease,
pubmed-meshheading:19678569-Foot-and-Mouth Disease Virus,
pubmed-meshheading:19678569-Genome, Viral,
pubmed-meshheading:19678569-Nucleic Acid Amplification Techniques,
pubmed-meshheading:19678569-RNA, Viral,
pubmed-meshheading:19678569-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:19678569-Sensitivity and Specificity,
pubmed-meshheading:19678569-Swine Vesicular Disease
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pubmed:year |
2009
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pubmed:articleTitle |
[Establishment of RT- LAMP for rapid detection of foot-and-mouth disease virus].
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pubmed:affiliation |
Shanghai Entry-Exit Inspection and Quarantine Bureau, Shanghai, China. lijiancq@yahoo.com.cn
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pubmed:publicationType |
Journal Article,
English Abstract
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