Carbon nanotube-assisted enhancement of surface plasmon resonance signal

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dc.contributor.authorEun Gyo Lee-
dc.contributor.authorKyung Mi Park-
dc.contributor.authorJin Young Jeong-
dc.contributor.authorS H Lee-
dc.contributor.authorJ E Baek-
dc.contributor.authorHong-Weon Lee-
dc.contributor.authorJoon Ki Jung-
dc.contributor.authorBong Hyun Chung-
dc.date.accessioned2020-09-23T13:15:19Z-
dc.date.available2020-09-23T13:15:19Z-
dc.date.issued2011-
dc.identifier.issn0003-2697-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/22566-
dc.description.abstractWe describe a method of amplifying the biosensing signal in surface plasmon resonance (SPR)-based immunoassays using an antibody-carbon nanotube (CNT) conjugate. As a model system, human erythropoietin (EPO) and human granulocyte macrophage colony-stimulating factor (GM-CSF) were detected by sandwich-type immunoassays using an SPR biosensor. For the amplification of the SPR signal, the CNT was conjugated with a polyclonal antibody, and then the conjugates were reacted with antibodies coupled with the target proteins. This amplification strategy increases the dynamic range of the immunoassays and enhances the detection sensitivity. The SPR immunoassays, combined with the CNT-assisted signal amplification method, provided a wide dynamic range over four orders of magnitude for both EPO and GM-CSF (0.1-1000. ng/ml). The CNT amplification method is expected to realize the detection of picogram levels and a wide dynamic detection range of multiple proteins, enabling it to offer a robust analysis tool for the development of biopharmaceutical production.-
dc.publisherElsevier-
dc.titleCarbon nanotube-assisted enhancement of surface plasmon resonance signal-
dc.title.alternativeCarbon nanotube-assisted enhancement of surface plasmon resonance signal-
dc.typeArticle-
dc.citation.titleAnalytical Biochemistry-
dc.citation.number2-
dc.citation.endPage211-
dc.citation.startPage206-
dc.citation.volume408-
dc.contributor.affiliatedAuthorEun Gyo Lee-
dc.contributor.affiliatedAuthorKyung Mi Park-
dc.contributor.affiliatedAuthorJin Young Jeong-
dc.contributor.affiliatedAuthorHong-Weon Lee-
dc.contributor.affiliatedAuthorJoon Ki Jung-
dc.contributor.affiliatedAuthorBong Hyun Chung-
dc.contributor.alternativeName이은교-
dc.contributor.alternativeName박경미-
dc.contributor.alternativeName정진영-
dc.contributor.alternativeName이승희-
dc.contributor.alternativeName백정은-
dc.contributor.alternativeName이홍원-
dc.contributor.alternativeName정준기-
dc.contributor.alternativeName정봉현-
dc.identifier.bibliographicCitationAnalytical Biochemistry, vol. 408, no. 2, pp. 206-211-
dc.identifier.doi10.1016/j.ab.2010.09.026-
dc.subject.keywordCarbon nanotube-
dc.subject.keywordErythropoietin-
dc.subject.keywordGranulocyte macrophage colony-stimulating factor-
dc.subject.keywordSurface plasmon resonance-
dc.subject.localCarbon nanotube-
dc.subject.localcarbon nanotubes-
dc.subject.localCarbon nanotubes-
dc.subject.localErythropoietin-
dc.subject.localerythropoietin-
dc.subject.localGranulocyte macrophage colony-stimulating factor-
dc.subject.localSurface Plasmon Resonance-
dc.subject.localSurfaceplasmonresonance-
dc.subject.localSurface plasmon resonance (SPR)-
dc.subject.localsurface plasmon resonance-
dc.subject.localSurface plasmon resonance-
dc.subject.localsurface plasmon resonance (SPR)-
dc.description.journalClassY-
Appears in Collections:
Division of Bio Technology Innovation > BioProcess Engineering Center > 1. Journal Articles
Division of Research on National Challenges > Environmental diseases research center > 1. Journal Articles
Division of Bio Technology Innovation > 1. Journal Articles
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