Presentation 1999/6/25
Development of DNA sensor for the detection of Escherichia coli O157
Kazunori Ikebukuro, Eriko Kai, Kazuyoshi Yano, Isao Karube,
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Abstract(in Japanese) (See Japanese page)
Abstract(in English) Polymerase chain reaction (PCR) products were detected using a flow injection type sensor based on surface plasmon resonance (SPR). Asymmetric PCR was used to amplify the target DNA sequence and two products with different length were produced. The novelty of our DNA detection system was that our target DNA was double stranded but the probe binding site, located in the 3-terminus, was single stranded. This avoids the formation of intra-and intermolecular complexes. This novel design permitted us not only to detect PCR product with high-sensitivity, but also to develop a rapid detection system for the detection of the verotoxin 2 gene of Escherichia coli O157:H7.
Keyword(in Japanese) (See Japanese page)
Keyword(in English) Escherichia coli O157:H7 / DNA detection / verotoxin / Surface plasmon resonance
Paper # OME99-34
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Committee OME
Conference Date 1999/6/25(1days)
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Paper Information
Registration To Organic Material Electronics (OME)
Language JPN
Title (in Japanese) (See Japanese page)
Sub Title (in Japanese) (See Japanese page)
Title (in English) Development of DNA sensor for the detection of Escherichia coli O157
Sub Title (in English)
Keyword(1) Escherichia coli O157:H7
Keyword(2) DNA detection
Keyword(3) verotoxin
Keyword(4) Surface plasmon resonance
1st Author's Name Kazunori Ikebukuro
1st Author's Affiliation Research Center for Advanced Science and Technology, University of Tokyo()
2nd Author's Name Eriko Kai
2nd Author's Affiliation Research Center for Advanced Science and Technology, University of Tokyo
3rd Author's Name Kazuyoshi Yano
3rd Author's Affiliation Research Center for Advanced Science and Technology, University of Tokyo
4th Author's Name Isao Karube
4th Author's Affiliation Research Center for Advanced Science and Technology, University of Tokyo
Date 1999/6/25
Paper # OME99-34
Volume (vol) vol.99
Number (no) 159
Page pp.pp.-
#Pages 5
Date of Issue