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dc.contributor.authorHejazi, MS
dc.contributor.authorPournaghi-Azar, MH
dc.contributor.authorAlipour, E
dc.contributor.authorAbdolahinia, ED
dc.contributor.authorArami, S
dc.contributor.authorNavvah, H
dc.date.accessioned2018-08-26T08:08:52Z
dc.date.available2018-08-26T08:08:52Z
dc.date.issued2011
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/50383
dc.description.abstractIn spite of the extensive attention paid on the development of various DNA detection strategies, very few studies have been reported regarding direct detection of DNA sequence and mutation in dsDNA. Here, we describe the feasibility of detection and discrimination of target DNA sequences and single base mutations (SBM) directly in double-stranded oligonucleotides and PCR products without the need for denaturation of the target dsDNA samples. This goal was achieved by employing a peptide nucleic acid (PNA) chain, self-assembled on the gold electrode as a probe, which binds to dsDNA and forms PNA-dsDNA hybrid.
dc.language.isoEnglish
dc.relation.ispartofELECTROANALYSIS
dc.subjectDNA hybridization biosensors
dc.subjectPeptide nucleic acid
dc.subjectPCR products
dc.subjectPNA-dsDNA hybrid
dc.subjectDNA
dc.titleDevelopment of a Novel Electrochemical Biosensor for Detection and Discrimination of DNA Sequence and Single Base Mutation in dsDNA Samples Based on PNA-dsDNA Hybridization - a new Platform Technology
dc.typeArticle
dc.citation.volume23
dc.citation.issue2
dc.citation.spage503
dc.citation.epage511
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1002/elan.201000413


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