Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/111042
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dc.titleNovel immunoblot assay using four recombinant antigens for diagnosis of Epstein-Barr virus primary infection and reactivation
dc.contributor.authorBuisson, M.
dc.contributor.authorFleurent, B.
dc.contributor.authorMak, M.
dc.contributor.authorMorand, P.
dc.contributor.authorChan, L.
dc.contributor.authorNg, A.
dc.contributor.authorGuan, M.
dc.contributor.authorChin, D.
dc.contributor.authorSeigneurin, J.M.
dc.date.accessioned2014-11-27T07:42:54Z
dc.date.available2014-11-27T07:42:54Z
dc.date.issued1999
dc.identifier.citationBuisson, M.,Fleurent, B.,Mak, M.,Morand, P.,Chan, L.,Ng, A.,Guan, M.,Chin, D.,Seigneurin, J.M. (1999). Novel immunoblot assay using four recombinant antigens for diagnosis of Epstein-Barr virus primary infection and reactivation. Journal of Clinical Microbiology 37 (8) : 2709-2714. ScholarBank@NUS Repository.
dc.identifier.issn00951137
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/111042
dc.description.abstractA new immunoblot assay, composed of four Epstein-Barr virus (EBV)- encoded recombinant proteins (virus capsid antigen [VCA] p23, early antigen [EA] p138, EA p54, and EBNA-1 p72), was compared with an immunofluorescence assay on a total of 291 sera. The test was accurate in 94.5% of cases of primary EBV infection, while an immunoglobulin G anti-VCA p23 band with strong intensity correlated with reactivation.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentBIOPROCESSING TECHNOLOGY CENTRE
dc.description.sourcetitleJournal of Clinical Microbiology
dc.description.volume37
dc.description.issue8
dc.description.page2709-2714
dc.description.codenJCMID
dc.identifier.isiutNOT_IN_WOS
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