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Please use this identifier to cite or link to this item: http://142.54.178.187:9060/xmlui/handle/123456789/16663
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dc.contributor.authorS. Hussain-
dc.contributor.authorTsukiboshi, Takao-
dc.contributor.authorUematsu, T.-
dc.date.accessioned2023-01-24T03:47:50Z-
dc.date.available2023-01-24T03:47:50Z-
dc.date.issued2000-06-06-
dc.identifier.citationHussain, S. H. A. U. K. A. T., Tsukiboshi, T. A. K. A. O., & Uematsu, T. S. U. T. O. M. U. (2000). Quick detection of Ascochyta lentis from lentil seeds using polymerase chain reaction (PCR) based techniques. Pakistan Journal of Botany, 32(1), 45-56.en_US
dc.identifier.issn2070-3368-
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/16663-
dc.description.abstractTwo Polymerase Chain Reaction (PCR) specific primers, ASCO1 and ASCO2 were developed for the detection of Ascochyta lentis from infected lentil seeds. PCR amplification with primers ASCO1 and ASCO2 resulted in amplification of an approximately 400bp product with A. lentis and A. rabiei isolates but not with A. fabae and other lentil pathogens viz., Sclerotinia sclerotiorum, Stemphylium botryosum and Colletotrichum lindemuthianum. The specific primers were amplified with the whole DNA of the A. lentis infected seeds but not with healthy seeds suggesting that the specific primers will provide a valuable tool for accurate and quick detection of A. lentis in lentil seeds.en_US
dc.language.isoenen_US
dc.publisherKarachi: Pakistan Botanical Societyen_US
dc.titleQuick detection of Ascochyta lentis from lentil seeds using Polymerase Chain Reaction (PCR) based techniquesen_US
dc.typeArticleen_US
Appears in Collections:Issue No. 1

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