Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/6517
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dc.contributor.authorThanseem, I-
dc.contributor.authorThulaseedharan, A-
dc.date.accessioned2009-11-11T05:31:02Z-
dc.date.available2009-11-11T05:31:02Z-
dc.date.issued2006-06-
dc.identifier.issn0975-1009 (Online); 0019-5189 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/6517-
dc.description492-498en_US
dc.description.abstractRQRT-PCR technique was evaluated for its validity as an alternative to Northern blotting for quantification of plant gene expression in diseased tissues of Hevea. Reliable RT-PCR results could be obtained by co-amplification of housekeeping actin gene as the internal control along with the gene of interest. The product of interest was quantified relative to that of the internal control by measuring net intensity of bands. Expression levels of defense-related -1,3-glucanase gene was studied in the pathogen infected tissues of rubber. The -1,3-glucanase gene was found to be induced in infected leaf tissues and reached a peak at 48 h after inoculation. The -1,3-glucanase gene expression during pathogen infection was determined through Northern blot hybridization also, using 18S RNA as the internal control. RQRT-PCR and Northern hybridization showed almost similar results, thereby validating the use of this technique to study the gene expression in rubber.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJEB Vol.44(06) [June 2006]en_US
dc.subjectActinen_US
dc.subject-1,3-Glucanaseen_US
dc.subjectHevea brasiliensisen_US
dc.subjectPhytophthoraen_US
dc.subjectRelative RT-PCRen_US
dc.titleOptimization of RQRT-PCR protocols to measure -1,3-glucanase mRNA levels in infected tissues of rubber tree (Hevea brasiliensis)en_US
dc.typeArticleen_US
Appears in Collections:IJEB Vol.44(06) [June 2006]

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