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Enzyme-linked immuno-strip biosensor to detect Escherichia coli O157 : H7

Authors
Park, SojungKim, HajinPaek, Se-HwanHong, Jong WookKim, Young-Kee
Issue Date
9월-2008
Publisher
ELSEVIER SCIENCE BV
Keywords
biosensor; ELISA; Escherichia coli O157 : H7; scanning electron microscope
Citation
ULTRAMICROSCOPY, v.108, no.10, pp.1348 - 1351
Indexed
SCIE
SCOPUS
Journal Title
ULTRAMICROSCOPY
Volume
108
Number
10
Start Page
1348
End Page
1351
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/122778
DOI
10.1016/j.ultramic.2008.04.063
ISSN
0304-3991
Abstract
A strip-based biosensor using the enzyme-linked immunosorbent assay technique was fabricated to detect Escherichia coli O157:H7. Two types of antibody specified to E. coli O15T:H7 were used to form sandwich-binding complexes. To fabricate an immuno-strip, capture antibody (monoclonal antibody) was immobilized onto signal generation pad and polyclonal antibody conjugated with horseradish peroxidase (HRP) was utilized as detection antibody. Four different functional membranes have been used to fabricate immuno-chromatographic assay strip. A sample application pad was a glass fiber membrane pre-treated with polyvinyl alcohol. A conjugate release pad was fabricated using a glass membrane. A signal generation pad was made on nitrocellulose membrane. Finally, a cellulose membrane was used as an absorption pad. Under optimal conditions of analysis, a color signal in proportion to the E. coli O157:H7 concentration was measured using a detector. The measurement range was 1.8 x 10(3)-1.8 x 10(8) CFU/mL. (C) 2008 Elsevier B.V. All rights reserved.
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