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dc.contributor.authorChangotra, Harish-
dc.contributor.authorSehajpal, Prabodh K.-
dc.date.accessioned2022-07-25T04:17:54Z-
dc.date.available2022-07-25T04:17:54Z-
dc.date.issued2013-
dc.identifier.urihttp://ir.juit.ac.in:8080/jspui//xmlui/handle/123456789/5118-
dc.descriptionIndian J. Virol. DOI 10.1007/s13337-013-0155-yen_US
dc.description.abstractStudies show that hepatitis B virus (HBV) DNA isolation methods vary in their efficiency to extract DNA from serum samples. The purpose of the present study was to develop an improved method for isolation of HBV DNA and compare it with commonly used HBV DNA isolation protocols. In order to develop HBV DNA isolation protocol, serum samples were collected from patients and screened for the presence of hepatitis B surface antigen, hepatitis B e antigen and HBV DNA. Highly viremic samples were pooled and used to compare commonly used HBV DNA isolation methods; namely alkaline lysis, microwave treatment, organic, inorganic with modified inorganic method. DNA isolated by these methods was detected qualitatively by polymerase chain reaction and quantitatively with competitive polymerase chain reaction (cPCR). The modified inorganic method gave maximum yield of HBV DNA followed by inorganic, organic, microwave treatment and alkaline lysis method.en_US
dc.language.isoenen_US
dc.publisherJaypee University of Information Technology, Solan, H.P.en_US
dc.subjectHBV DNAen_US
dc.subjectIsolationen_US
dc.subjectQuantificationen_US
dc.subjectAntiviral treatmenten_US
dc.titleAn Improved Method for the Isolation of Hepatitis B Virus DNA from Human Serumen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles

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