Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/14016
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dc.contributor.authorVidhya, S Shree-
dc.contributor.authorGowda, P H Ramanjini-
dc.contributor.authorYogendra, K N-
dc.contributor.authorNingaraju, T M-
dc.contributor.authorSalome, T-
dc.date.accessioned2012-05-02T04:13:28Z-
dc.date.available2012-05-02T04:13:28Z-
dc.date.issued2012-04-
dc.identifier.issn0975-0967 (Online); 0972-5849 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/14016-
dc.description176-181en_US
dc.description.abstractDetection of genetically modified (GM) crops and products are necessary to comply with international labeling regulations and to avoid spurious and unapproved GM planting. DNA based analytical tools involving PCR and real-time PCR were used to detect GM cotton seeds. Four pairs of primers specific for CaMV 35S, Nos, nptII and cry1Ac genes were used for the DNA detection of GM crop. The limit of detection in real-time PCR was found to be 0.1%. Evidently, these two PCR techniques were successful in detecting transgenes in the DNA of GM cotton seeds.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJBT Vol.11(2) [April 2012]en_US
dc.subjectDetection methoden_US
dc.subjectGM cotton seedsen_US
dc.subjectLabeling regulationsen_US
dc.subjectPCRen_US
dc.subjectReal-time PCRen_US
dc.titleDetection of genetically modified cotton seeds using PCR and real-time PCRen_US
dc.typeArticleen_US
Appears in Collections:IJBT Vol.11(2) [April 2012]

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