Evaluation of a probe hybridisation serotyping method for group A rotavirus

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dc.contributor.authorAli, Ayub-
dc.contributor.authorBingnan, Fu-
dc.contributor.authorUnicomb, Leanne E.-
dc.contributor.authorRahim, Zeaur-
dc.contributor.authorHossain, Ashfaque-
dc.contributor.authorTzipori, Saul-
dc.date.accessioned2007-11-04T02:38:36Z-
dc.date.available2007-11-04T02:38:36Z-
dc.date.issued1993-
dc.identifier.citationJ Diarrhoeal Dis Res 1993 Sep;11(3):153-6-
dc.identifier.issn0253-8768-
dc.identifier.urihttp://hdl.handle.net/123456789/275-
dc.description.abstractSerotype-specificity and sensitivity of oligonucleotide probes to serotype human rotavinises was assessed. Probes could detect as little as 63 ng of homologous RNA and none reacted with as much as 100 ng of hcterologous RNA. Northern-blot analysis revealed that probes reacted with one of genomic segments 7, 8 or 9 of corresponding serotypesen
dc.format.extent173988 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isoenen
dc.subjectRotavirusen
dc.subjectOligonucleotide probesen
dc.subjectElectrophoresisen
dc.subjectSerotypingsen
dc.titleEvaluation of a probe hybridisation serotyping method for group A rotavirusen
dc.typeArticleen
Appears in Collections:Laboratory sciences research papers

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