Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/18979
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dc.contributor.authorPrasad, G-
dc.contributor.authorMinakshi-
dc.date.accessioned2013-06-12T08:44:50Z-
dc.date.available2013-06-12T08:44:50Z-
dc.date.issued1999-02-
dc.identifier.issn0975-1009 (Online); 0019-5189 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/18979-
dc.description157-160en_US
dc.description.abstractBluetongue virus serotype 1 (Avikanagar isolate) was grown in BHK-21 cell line and titrated. The titre of the virus in BHK-21 cell line was 106 TCID50/ml . RNA-polyacrylamide gel electrophoresis (RNA-PAGE) and dot immunobinding assay (DIA) were performed on to-fold serial dilutions of the sonicated cell culture material. The results indicated that the minimum limit of detection of the virus by RNA- PAGE and DIA was 105 TCID50/ml.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJEB Vol.37(02) [February 1999]en_US
dc.titleComparative evaluation of sensitivity of RNA-polyacrylamide gel electrophoresis and dot immunobinding assay for detection of bluetongue virus in cell cultureen_US
dc.typeArticleen_US
Appears in Collections:IJEB Vol.37(02) [February 1999]

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