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Cited 69 time in webofscience Cited 71 time in scopus
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dc.contributor.authorHong, BJ-
dc.contributor.authorSunkara, V-
dc.contributor.authorPark, JW-
dc.date.accessioned2015-06-25T02:53:46Z-
dc.date.available2015-06-25T02:53:46Z-
dc.date.created2009-03-16-
dc.date.issued2005-01-
dc.identifier.issn0305-1048-
dc.identifier.other2015-OAK-0000005296en_US
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/11835-
dc.description.abstractWe have developed new surface to ensure a proper spacing between immobilized biomolecules. While DNA microarray on this surface provided each probe DNA with ample space for hybridization with incoming target DNAs, the microarray showed enhanced discrimination efficiency for various types of single nucleotide polymorphism. The high discrimination efficiency holds for all tested cases (100:< 1 for internal mismatched cases; 100:< 28 for terminal mismatched ones). In addition, by investigating influence of hybridization temperature and washing condition on the fluorescence intensity and the discrimination efficiency with and without controlled mesospacing, it was observed that the nanoscale-controlled surface showed good discrimination efficiency in a wide range of temperature (37-50 degrees C), and hybridization behavior on the surface was in agreement with the solution one. Intriguingly, it was found that washing process after the hybridization was critical for the high discrimination efficiency. For the particular case, washing process was so efficient that only 30 s washing was sufficient to reach the optimal discrimination ratio.-
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.titleDNA microarrays on nanoscale-controlled surface-
dc.typeArticle-
dc.contributor.college화학과en_US
dc.identifier.doi10.1093/NAR/GNI109-
dc.author.googleHong, BJen_US
dc.author.googleSunkara, Ven_US
dc.author.googlePark, JWen_US
dc.relation.volume33en_US
dc.relation.issue12en_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.33, no.12-
dc.identifier.wosid000230725400004-
dc.date.tcdate2019-01-01-
dc.citation.number12-
dc.citation.titleNUCLEIC ACIDS RESEARCH-
dc.citation.volume33-
dc.contributor.affiliatedAuthorPark, JW-
dc.identifier.scopusid2-s2.0-26444500193-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc57-
dc.description.scptc37*
dc.date.scptcdate2018-10-274*
dc.type.docTypeArticle-
dc.subject.keywordPlusSELF-ASSEMBLED MONOLAYERS-
dc.subject.keywordPlusPROTEIN ADSORPTION-
dc.subject.keywordPlusMODEL SYSTEM-
dc.subject.keywordPlusHYBRIDIZATION-
dc.subject.keywordPlusDENDRIMERS-
dc.subject.keywordPlusLIGANDS-
dc.subject.keywordPlusBINDING-
dc.subject.keywordPlusRESIST-
dc.subject.keywordPlusSAMS-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-

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