DC Field | Value | Language |
---|---|---|
dc.contributor.author | C H Kim | - |
dc.contributor.author | J H Ahn | - |
dc.contributor.author | J Y Kim | - |
dc.contributor.author | J M Choi | - |
dc.contributor.author | K C Lim | - |
dc.contributor.author | T J Park | - |
dc.contributor.author | N S Heo | - |
dc.contributor.author | Hee Gu Lee | - |
dc.contributor.author | J W Kim | - |
dc.contributor.author | Y K Choi | - |
dc.date.accessioned | 2017-04-19T09:35:58Z | - |
dc.date.available | 2017-04-19T09:35:58Z | - |
dc.date.issued | 2013 | - |
dc.identifier.issn | 0956-5663 | - |
dc.identifier.uri | 10.1016/j.bios.2012.08.047 | ko |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/11109 | - |
dc.description.abstract | Most of point-of-care testing (POCT) to improve facilitates in diagnosis, treatment, and monitoring of patients. POCT technique has still remained a quantitatively and accurately detective effect. In this article, we demonstrated that real human C-reactive protein (CRP) in serum was detected for a chip-based point-of-care testing application based on a nanogap-embedded field effect transistor (FET), and the results were compared with those obtained via the enzyme-linked immunosorbent assay (ELISA) method. The limit of detection (LOD), determined from the standard curve, was 0.1. ng/ml, which is comparable to that of commercialized ELISAs. We evaluated that an improved detection range (0.1. ng/ml to 100. ng/ml) was achieved by comparing with commercialized ELISA. Control experiments to determine selectivity and to discern false-positive/false-negative rates were also performed. This report is the first description of the detection of CRP in human serum using a silicon-based biosensor. | - |
dc.publisher | Elsevier | - |
dc.title | CRP detection from serum for chip-based point-of-care testing system | - |
dc.title.alternative | CRP detection from serum for chip-based point-of-care testing system | - |
dc.type | Article | - |
dc.citation.title | Biosensors & Bioelectronics | - |
dc.citation.number | 1 | - |
dc.citation.endPage | 327 | - |
dc.citation.startPage | 322 | - |
dc.citation.volume | 41 | - |
dc.contributor.affiliatedAuthor | Hee Gu Lee | - |
dc.contributor.alternativeName | 김창훈 | - |
dc.contributor.alternativeName | 안재혁 | - |
dc.contributor.alternativeName | 김지연 | - |
dc.contributor.alternativeName | 최지민 | - |
dc.contributor.alternativeName | 임경춘 | - |
dc.contributor.alternativeName | 박태정 | - |
dc.contributor.alternativeName | 허남수 | - |
dc.contributor.alternativeName | 이희구 | - |
dc.contributor.alternativeName | 김종완 | - |
dc.contributor.alternativeName | 최양규 | - |
dc.identifier.bibliographicCitation | Biosensors & Bioelectronics, vol. 41, no. 1, pp. 322-327 | - |
dc.identifier.doi | 10.1016/j.bios.2012.08.047 | - |
dc.subject.keyword | C-reactive protein | - |
dc.subject.keyword | CRP | - |
dc.subject.keyword | FET-based biosensor | - |
dc.subject.keyword | Nanogap-embedded FET | - |
dc.subject.keyword | Point-of-care testing (POCT) | - |
dc.subject.local | C-reactive protein | - |
dc.subject.local | C-reactive protein (CRP) | - |
dc.subject.local | CRP | - |
dc.subject.local | FET-based biosensor | - |
dc.subject.local | Nanogap-embedded FET | - |
dc.subject.local | Point-of-care testing (POCT) | - |
dc.subject.local | point of care testing | - |
dc.subject.local | Point-of-care testing | - |
dc.subject.local | point-of-care-testing | - |
dc.subject.local | Point-of-care test (POCT) | - |
dc.subject.local | POCT | - |
dc.subject.local | PoCT | - |
dc.subject.local | Point of care testing | - |
dc.subject.local | Point-of-care test | - |
dc.subject.local | Point of Care Testing | - |
dc.subject.local | point-of-care testing (POCT) | - |
dc.description.journalClass | Y | - |
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