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Poly(dimethyl siloxane)-based protein chip for simultaneous detection of multiple samples: Use of glycidyl methacrylate photopolymer for site-specific protein immobilization

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dc.contributor.authorPark, Kyoung Hwan-
dc.contributor.authorPark, Hyun Gyu-
dc.contributor.authorKim, Joon-Ho-
dc.contributor.authorSeong, Ki Hun-
dc.date.accessioned2021-06-23T21:02:31Z-
dc.date.available2021-06-23T21:02:31Z-
dc.date.issued2006-12-
dc.identifier.issn0956-5663-
dc.identifier.issn1873-4235-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/44421-
dc.description.abstractThis paper describes fabrication of a poly(dimethyl siloxane) (PDMS)-based chip to analyze multiple protein interactions utilizing glycidyl methacrylate (GMA) photopolymer for a site-specific immobilization of capture proteins in a closed system. First, using one direction channels of a PDMS mold having cross-channels, GMA micropads were prepared by photopolymerizing GMA solution by 365 nm light irradiation at predetermined positions. After the first mold was replaced with a second mold having higher height or directly without mold changing, capture proteins were allowed to be covalently immobilized onto the surface of the epoxide-activated GMA pads. Following immobilization, poly(ethylene glycol) diacrylate (PEG-DA) precursor was photopolymerized at specific regions to generate plugs for prevention of mixing between different sample injection channels, diminishing the need of a mold changing for sample injections. Final chip was assembled by connecting separated sample injection channels using a connector mold. The viability of this strategy was successfully demonstrated by simultaneous detection of two different antigen-antibody interactions. (c) 2006 Elsevier B.V. All rights reserved.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER ADVANCED TECHNOLOGY-
dc.titlePoly(dimethyl siloxane)-based protein chip for simultaneous detection of multiple samples: Use of glycidyl methacrylate photopolymer for site-specific protein immobilization-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.bios.2006.01.029-
dc.identifier.scopusid2-s2.0-33750969698-
dc.identifier.wosid000242230800006-
dc.identifier.bibliographicCitationBIOSENSORS & BIOELECTRONICS, v.22, no.5, pp 613 - 620-
dc.citation.titleBIOSENSORS & BIOELECTRONICS-
dc.citation.volume22-
dc.citation.number5-
dc.citation.startPage613-
dc.citation.endPage620-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaElectrochemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.relation.journalWebOfScienceCategoryElectrochemistry-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.subject.keywordPlusMICROFLUIDIC SYSTEMS-
dc.subject.keywordPlusFABRICATION-
dc.subject.keywordPlusDNA-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusHYDROGELS-
dc.subject.keywordPlusPOLYMER-
dc.subject.keywordPlusMICROSTRUCTURES-
dc.subject.keywordPlusMICROARRAY-
dc.subject.keywordPlusMICROCHIP-
dc.subject.keywordPlusARRAYS-
dc.subject.keywordAuthorglycidyl methacrylate-
dc.subject.keywordAuthorpoly(dimethyl siloxane) (PDMS)-
dc.subject.keywordAuthormicrofluidics-
dc.subject.keywordAuthorpoly(ethylene glycol) diacrylate-
dc.subject.keywordAuthorbiomolecular immobilization-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0956566306000509?via%3Dihub-
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ERICA 공학대학 (DEPARTMENT OF BIONANO ENGINEERING)
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