Optimization of DNA Isolation and RAPD Technique in Arecanut (Areca catechu L.)

dc.contributor.authorRajesh, M.K.
dc.contributor.authorBharathi, M.
dc.contributor.authorNagarajan, P.
dc.date.accessioned2014-10-16T05:08:14Z
dc.date.available2014-10-16T05:08:14Z
dc.date.issued2007
dc.description.abstractA simple and efficient protocol for extracting high quality DNA from arecanut (Areca catechu L.) leaves is presented. DNA yield and purity were monitored by gel electrophoresis and by determining absorbance at UV (A260/A280). The ratio was between 1.7 to 1.9 indicating that the presence of contaminating metabolites was minimal. The quantities of DNA obtained were 100- 400 ig/g starting material. The isolated DNA proved amenable to PCR amplification and restriction digestion. DNA was completely digested with the three restriction enzymes (EcoR I, EcoR V and Hind III) confirming the purity of the extracted DNA. Using the isolated DNA, the parameters for randomly amplified polymorphic DNA (RAPD) protocol was standardized.en_US
dc.identifier.citationAgrotrópica 19: 31 - 34. 2007.en_US
dc.identifier.urihttp://hdl.handle.net/123456789/6019
dc.language.isoenen_US
dc.subjectArecanut palmen_US
dc.subjectgel electrophoresisen_US
dc.subjectenzimesen_US
dc.subjectEcoR Ien_US
dc.subjectEcoR Ven_US
dc.subjectHind IIIen_US
dc.titleOptimization of DNA Isolation and RAPD Technique in Arecanut (Areca catechu L.)en_US
dc.typeArticleen_US

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