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Cited 78 time in webofscience Cited 76 time in scopus
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dc.contributor.authorSung Hee Ko-
dc.contributor.authorSung Jae Kim-
dc.contributor.authorLih Feng Cheow-
dc.contributor.authorLeon D. Li-
dc.contributor.authorKang, KH-
dc.contributor.authorJongyoon Han-
dc.date.accessioned2015-06-25T02:37:58Z-
dc.date.available2015-06-25T02:37:58Z-
dc.date.created2011-04-18-
dc.date.issued2011-01-
dc.identifier.issn1473-0197-
dc.identifier.other2015-OAK-0000022816en_US
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/11336-
dc.description.abstractA massively parallel nanofluidic concentration device array for multiplexed and high-throughput biomolecule detection is demonstrated. By optimizing the microchannel/nanojunction design and channel conductivity, an array of up to 128 nanofluidic concentration devices were fabricated. Operation of the entire array requires only one inlet and one outlet reservoir, with the application of a single operational voltage bias across them. Concentration efficiencies of the devices were found to be uniform within the array, within 5% error. Alternatively, concentration speed in each channel can be individually tuned by controlling the length of the inlet microchannel and thus controlling the flow rate based on change of the tangential electric field. This allows immuno-binding reactions at different concentration ranges to be performed in parallel. Using multiplexed, successive-concentration enhanced detection in the device, we have shown that the dynamic range and reliability of the immunoassay can be significantly increased.-
dc.description.statementofresponsibilityopenen_US
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.relation.isPartOfLAB ON A CHIP-
dc.rightsBY_NC_NDen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.0/kren_US
dc.titleMassively parallel concentration device for multiplexed immunoassays-
dc.typeArticle-
dc.contributor.college기계공학과en_US
dc.identifier.doi10.1039/C0LC00349B-
dc.author.googleKo, SHen_US
dc.author.googleKim, SJen_US
dc.author.googleHan, Jen_US
dc.author.googleKang, KHen_US
dc.author.googleLi, LDen_US
dc.author.googleCheow, LFen_US
dc.relation.volume11en_US
dc.relation.issue7en_US
dc.relation.startpage1351en_US
dc.relation.lastpage1358en_US
dc.contributor.id10107580en_US
dc.relation.journalLAB ON A CHIPen_US
dc.relation.indexSCI급, SCOPUS 등재논문en_US
dc.relation.sciSCIen_US
dc.collections.nameJournal Papersen_US
dc.type.rimsART-
dc.identifier.bibliographicCitationLAB ON A CHIP, v.11, no.7, pp.1351 - 1358-
dc.identifier.wosid000288455100023-
dc.date.tcdate2019-01-01-
dc.citation.endPage1358-
dc.citation.number7-
dc.citation.startPage1351-
dc.citation.titleLAB ON A CHIP-
dc.citation.volume11-
dc.contributor.affiliatedAuthorKang, KH-
dc.identifier.scopusid2-s2.0-79952664169-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc56-
dc.description.scptc54*
dc.date.scptcdate2018-10-274*
dc.type.docTypeArticle-
dc.subject.keywordPlusPROTEOME ANALYSIS-
dc.subject.keywordPlusMICROFLUIDIC CHIP-
dc.subject.keywordPlusNANOFLUIDIC PRECONCENTRATOR-
dc.subject.keywordPlusCONCENTRATION POLARIZATION-
dc.subject.keywordPlusCAPILLARY-ELECTROPHORESIS-
dc.subject.keywordPlusSAMPLE PRECONCENTRATION-
dc.subject.keywordPlusGEL-ELECTROPHORESIS-
dc.subject.keywordPlusMASS-SPECTROMETRY-
dc.subject.keywordPlusHUMAN PLASMA-
dc.subject.keywordPlusSTACKING-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryInstruments & Instrumentation-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaInstruments & Instrumentation-

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