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dc.contributor.author김연상-
dc.date.accessioned2018-05-30T08:14:01Z-
dc.date.available2018-05-30T08:14:01Z-
dc.date.issued2006-
dc.identifier.issn0956-5663-
dc.identifier.otherOAK-3287-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/243480-
dc.description.abstractHerein, we present the fabrication of well-defined micro-reservoirs and a simple strategy to immobilize biomolecules selectively inside the reservoirs. The micro-reservoirs are fabricated using a photocurable prepolymer, which enables the formation of concrete structures with high-fidelity, so that the reservoirs are spatially-segregated from each other by rigid physical barriers. For the directed binding of the protein, two steps are involved. First, poly(ethylene glycol) (PEG) is contact-printed on those areas where the protein binding is not desired, and next, protein binding is promoted where desired via carbodiimide chemistry. Fluorescein-tagged albumin is successfully immobilized inside the micro-reservoirs and microchannel arrays with high sensitivity, regardless of the sizes of the reservoirs and channels. The proposed system can be used for constructing multi-functional biosensors by immobilizing individual bioorganisms specifically in each micro-reservoir or microchannel. © 2005 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.titleSelective patterning and immobilization of biomolecules within precisely-defined micro-reservoirs-
dc.typeArticle-
dc.relation.issue11-
dc.relation.volume21-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage2188-
dc.relation.lastpage2193-
dc.relation.journaltitleBiosensors and Bioelectronics-
dc.identifier.doi10.1016/j.bios.2005.11.003-
dc.identifier.wosidWOS:000236959400023-
dc.identifier.scopusid2-s2.0-33645848751-
dc.author.googleLee N.Y.-
dc.author.googleLim J.R.-
dc.author.googleKim Y.S.-
dc.contributor.scopusid김연상(8938854200)-
dc.date.modifydate20211210152421-
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자연과학대학 > 화학·나노과학전공 > Journal papers
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