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Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/834
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dc.contributor.authorKumar, A-
dc.contributor.authorANANDARAJ, M-
dc.date.accessioned2017-11-15T10:14:11Z-
dc.date.available2017-11-15T10:14:11Z-
dc.date.issued2006-
dc.identifier.citationIndian Phytopath., Vol.59 (2), (2006), pp.154-160en_US
dc.identifier.urihttp://hdl.handle.net/123456789/834-
dc.description.abstractAn efficient DNA isolation protocol and PCR based detection of bacterial pathogen in soil are described here. The use of this DNA isolation protocol and PCR based method using universal Ralstonia solanacearum specific primer offer a rapid method for unambiguous detection of this pathogen in soil which can be employed for monitoring soil. The PCR based assay could detect the pathogen at a concentration of 103-104cells per gram of soil.en_US
dc.subjectPCRen_US
dc.subjectspecific primersen_US
dc.subjectRalstonia solanacearumen_US
dc.subjectgingeren_US
dc.titleMethod for isolation of soil DNA and PCR based detection of ginger wilt pathogen, Ralstonia solanacearumen_US
dc.typeArticleen_US
Appears in Collections:CROP PROTECTION

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