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dc.creatorTsakogiannis, D.en
dc.creatorPapacharalampous, M.en
dc.creatorToska, E.en
dc.creatorKyriakopoulou, Z.en
dc.creatorDimitriou, T. G.en
dc.creatorRuether, I. G. A.en
dc.creatorKomiotis, D.en
dc.creatorMarkoulatos, P.en
dc.date.accessioned2015-11-23T10:50:38Z
dc.date.available2015-11-23T10:50:38Z
dc.date.issued2015
dc.identifier10.1016/j.mcp.2014.09.003
dc.identifier.issn0890-8508
dc.identifier.urihttp://hdl.handle.net/11615/33761
dc.description.abstractLong-term infection with high-risk HPV genotypes is the leading cause of cervical cancer. In the present study a Duplex Real-time PCR assay was developed in order to identify HPV types 16, 18, 31, 35, 51 and 66 in three reactions, through SYBR green I melting curve analysis. The method utilizes type-specific primer sets that allowed the amplification of highly conserved regions of L1 gene. Reconstitution experiments were conducted by using HPV DNA plasmids in order to determine the sensitivity of the assay. The newly designed assay has a limit of detection of 10 copies per reaction. The most prevalent HPV genotype in single and in multiple HPV infections was HPV16 followed by HPV18, HPV51, HPV31, HPV35 and HPV66. The proposed method is a simple, specific, sensitive and cost-effective assay that can be easily incorporated in small and medium size laboratories for the rapid identification of the most clinically important HPV genotypes. (C) 2014 Elsevier Ltd. All rights reserved.en
dc.sourceMolecular and Cellular Probesen
dc.source.uri<Go to ISI>://WOS:000350532300003
dc.subjectHPV genotypingen
dc.subjectDuplex Real-time PCRen
dc.subjectMelting curve analysisen
dc.subjectL1 geneen
dc.subjectHUMAN-PAPILLOMAVIRUS INFECTIONen
dc.subjectCERVICAL CYTOLOGYen
dc.subjectMULTIPLE TYPESen
dc.subjectCANCERen
dc.subjectRISKen
dc.subjectDNAen
dc.subjectCLASSIFICATIONen
dc.subjectWOMENen
dc.subjectBiochemical Research Methodsen
dc.subjectBiochemistry & Molecular Biologyen
dc.subjectBiotechnology & Applied Microbiologyen
dc.subjectCell Biologyen
dc.titleDuplex Real-time PCR assay and SYBR green I melting curve analysis for molecular identification of HPV genotypes 16, 18, 31, 35, 51 and 66en
dc.typejournalArticleen


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