Please use this identifier to cite or link to this item:
http://nopr.niscair.res.in/handle/123456789/11302
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Gupta, A K | - |
dc.contributor.author | Ahlawat, Anita | - |
dc.contributor.author | Bhatia, Vandanajay | - |
dc.date.accessioned | 2011-03-22T06:17:28Z | - |
dc.date.available | 2011-03-22T06:17:28Z | - |
dc.date.issued | 2003-04 | - |
dc.identifier.issn | 0975-0967 (Online); 0972-5849 (Print) | - |
dc.identifier.uri | http://hdl.handle.net/123456789/11302 | - |
dc.description | 214-219 | en_US |
dc.description.abstract | Reverse transcriptase-polymerase chain reaction (RT-PCR) and RNA : DNA hybridization based diagnostic techniques were standardized and used for rapid and specific detection of equine influenza virus. RT -PCR technique based on amplification of both Non-structural-l (NS1) and Neuraminidase (NA) genes was standardized. Beside this, RNA-DNA hybridization technique using both non-structural and neuraminidase gene segments specific hot probes was also developed to directly detect this virus with out involving viral RNA isolation. Both RT-PCR and RNA-DNA hybridization techniques were successfully used for detection of influenza virus in samples within 24 to 48 hrs. These techniques can now be used as a routine tests in the laboratory for detection of influenza virus from field samples. | en_US |
dc.language.iso | en_US | en_US |
dc.publisher | NISCAIR-CSIR, India | en_US |
dc.rights | ![]() | en_US |
dc.source | IJBT Vol.02(2) [April 2003] | en_US |
dc.subject | Equine influenza | en_US |
dc.subject | RT-PCR | en_US |
dc.subject | Nucleic acid hybridization | en_US |
dc.title | Detection of Equine Influenza Viral Genome by RT-PCR and RNA-DNA Hybridization | en_US |
dc.type | Article | en_US |
Appears in Collections: | IJBT Vol.02(2) [April 2003] |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
IJBT 2(2) 214-219.pdf | 1.3 MB | Adobe PDF | View/Open |
Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.