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Cited 18 time in webofscience Cited 20 time in scopus
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dc.contributor.authorJung, YJ-
dc.contributor.authorAlbrecht, JA-
dc.contributor.authorKwak, JW-
dc.contributor.authorPark, JW-
dc.date.accessioned2015-06-25T02:54:06Z-
dc.date.available2015-06-25T02:54:06Z-
dc.date.created2013-05-31-
dc.date.issued2012-12-
dc.identifier.issn0305-1048-
dc.identifier.other2015-OAK-0000027621en_US
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/11845-
dc.description.abstractForce-based atomic force microscopy (AFM) was used to detect HCV (hepatitis C virus) RNA directly and to quantitatively analyse it without the need for reverse transcription or amplification. Capture and detection DNA probes were designed. The former was spotted onto a substrate with a conventional microarrayer, and the latter was immobilized on an AFM probe. To control the spacing between the immobilized DNAs on the surface, dendron self-assembly was employed. Force-distance curves showed that the mean force of the specific unbinding events was 32 +/- 5 pN, and the hydrodynamic distance of the captured RNA was 30-60 nm. Adhesion force maps were generated with criteria including the mean force value, probability of obtaining the specific curves and hydrodynamic distance. The maps for the samples whose concentrations ranged from 0.76 fM to 6.0 fM showed that cluster number has a linear relationship with RNA concentration, while the difference between the observed number and the calculated one increased at low concentrations. Because the detection limit is expected to be enhanced by a factor of 10 000 when a spot of 1 micron diameter is employed, it is believed that HCV RNA of a few copy numbers can be detected by the use of AFM.-
dc.description.statementofresponsibilityopenen_US
dc.languageEnglish-
dc.publisherOXFORD UNIV PRESS-
dc.relation.isPartOfNUCLEIC ACIDS RESEARCH-
dc.rightsBY_NC_NDen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.0/kren_US
dc.titleDirect quantitative analysis of HCV RNA by atomic force microscopy without labeling or amplification-
dc.typeArticle-
dc.contributor.college화학과en_US
dc.identifier.doi10.1093/NAR/GKS953-
dc.author.googleJung, YJen_US
dc.author.googleAlbrecht, JAen_US
dc.author.googlePark, JWen_US
dc.author.googleKwak, JWen_US
dc.relation.volume40en_US
dc.relation.issue22en_US
dc.relation.startpage11728en_US
dc.relation.lastpage11736en_US
dc.contributor.id10053210en_US
dc.relation.journalNUCLEIC ACIDS RESEARCHen_US
dc.relation.indexSCI급, SCOPUS 등재논문en_US
dc.relation.sciSCIen_US
dc.collections.nameJournal Papersen_US
dc.type.rimsART-
dc.identifier.bibliographicCitationNUCLEIC ACIDS RESEARCH, v.40, no.22, pp.11728 - 11736-
dc.identifier.wosid000313414800054-
dc.date.tcdate2019-01-01-
dc.citation.endPage11736-
dc.citation.number22-
dc.citation.startPage11728-
dc.citation.titleNUCLEIC ACIDS RESEARCH-
dc.citation.volume40-
dc.contributor.affiliatedAuthorPark, JW-
dc.identifier.scopusid2-s2.0-84871219195-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc15-
dc.description.scptc14*
dc.date.scptcdate2018-10-274*
dc.type.docTypeArticle-
dc.subject.keywordPlusHEPATITIS-C-
dc.subject.keywordPlusCLINICAL UTILITY-
dc.subject.keywordPlusDNA MICROARRAYS-
dc.subject.keywordPlusPCR-
dc.subject.keywordPlusQUANTIFICATION-
dc.subject.keywordPlusTECHNOLOGIES-
dc.subject.keywordPlusSPECTROSCOPY-
dc.subject.keywordPlusEFFICIENCY-
dc.subject.keywordPlusMOLECULES-
dc.subject.keywordPlusBLOOD-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-

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