Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/7758
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dc.contributor.authorGhosh, S B-
dc.contributor.authorBapat, V A-
dc.date.accessioned2010-03-31T06:32:16Z-
dc.date.available2010-03-31T06:32:16Z-
dc.date.issued2006-04-
dc.identifier.issn0975-0967 (Online); 0972-5849 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/7758-
dc.description232-235en_US
dc.description.abstractA reverse transcription polymerase chain reaction (RT-PCR) based protocol with a pair of potato virus Y coat protein gene specific primers was found to be more sensitive method for the PVY detection in infected tobacco leaf and potato tuber tissues than conventional enzyme linked immunosorbent assay (ELISA) or nucleic acid spot hybridization (NASH) based methods. It was found in our studies that by RT-PCR, the presence of the virus could be detected in potato tubers of two field samples, which could not be detected by NASH or ELISA.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt. Cl.8 C12N15/10en_US
dc.sourceIJBT Vol.5(2) [April 2006]en_US
dc.subjectELISAen_US
dc.subjectNASHen_US
dc.subjectpotato virus Y (PVY)en_US
dc.subjectRT-PCRen_US
dc.titleDevelopment of RT-PCR based method for detection of potato virus Y in tobacco and potatoen_US
dc.typeArticleen_US
Appears in Collections:IJBT Vol.05(2) [April 2006]

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