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dc.contributor.authorGaspar, J. O.-
dc.contributor.authorBelintani, P.-
dc.contributor.authorAlmeida, A. M. R.-
dc.contributor.authorKitajima, E. W.-
dc.date.accessioned2014-05-20T14:03:45Z-
dc.date.accessioned2016-10-25T17:09:49Z-
dc.date.available2014-05-20T14:03:45Z-
dc.date.available2016-10-25T17:09:49Z-
dc.date.issued2008-03-01-
dc.identifierhttp://dx.doi.org/10.1016/j.jviromet.2007.11.005-
dc.identifier.citationJournal of Virological Methods. Amsterdam: Elsevier B.V., v. 148, n. 1-2, p. 283-285, 2008.-
dc.identifier.issn0166-0934-
dc.identifier.urihttp://hdl.handle.net/11449/22420-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/22420-
dc.description.abstractSequences of the coat protein amino acids of definitive and tentative species of carlaviruses deposited in GenBank were aligned and a region of seven amino acids (GLGVPTE) was found to be conserved. The corresponding nucleotides were aligned, allowing the design of a degenerate primer that together with an oligo dT anti-sense primer, was effective for the detection of three distinct carlavirus species, two transmitted by aphids and one by whitefly. These primers have the advantage that about 940 nt from the 3'-terminus, comprising part of the CP gene (about 60%), the 11 K gene, and the terminal untranslated region can be amplified for sequencing. The fact that this amino acid sequence is conserved in almost all of the sequenced carlaviruses, allows the prediction that this primer pair will be useful as a diagnostic tool for carlavirus species. (C) 2007 Elsevier B.V. All rights reserved.en
dc.format.extent283-285-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectcarlavirus identificationen
dc.subjectdiagnosisen
dc.subjectFlexiviridaeen
dc.subjectRT-PCRen
dc.titleA degenerate primer allows amplification of part of the 3 '-terminus of three distinct carlavirus speciesen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionEmpresa Brasileira de Pesquisa Agropecuária (EMBRAPA)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.description.affiliationUNESP Univ Estadual Paulista, Dept Bot & Zool, BR-15054000 Sao Jose do Rio Preto, SP, Brazil-
dc.description.affiliationEmpresa Brasileira de Pesquisa Agropecuária (EMBRAPA) Soja, BR-86001970 Londrina, PR, Brazil-
dc.description.affiliationESALQ, BR-13418900 Piracicaba, SP, Brazil-
dc.description.affiliationUnespUNESP Univ Estadual Paulista, Dept Bot & Zool, BR-15054000 Sao Jose do Rio Preto, SP, Brazil-
dc.identifier.doi10.1016/j.jviromet.2007.11.005-
dc.identifier.wosWOS:000254720500038-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Virological Methods-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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