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dc.contributor.author박성수-
dc.date.accessioned2016-08-28T11:08:43Z-
dc.date.available2016-08-28T11:08:43Z-
dc.date.issued2004-
dc.identifier.issn0022-1147-
dc.identifier.otherOAK-2320-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/219463-
dc.description.abstractWe report the development of automated flourometric immunoassay for the detection of Escherichia coli O157:H7, using antibody-directed liposomes (immunoliposomes) encapsulating fluorophore as an analytical reagent. Thiolated antibodies (anti-E. coli O157:H7) were coupled to malemide-tagged liposomes encapsulating dye. To automate the assay, a fluorescence plate reader was included in the assay system to detect fluorophore released from lysed liposomes in a microplate. The detection limit of the current assay with pure cultures of the serotype was about 104 colony-forming units (CFU)/mL. The assay can detect E. coli O157 in ground beef samples inoculated with as few as 0.8 CFU/mL after a 12-h enrichment. These results demonstrate the feasibility of using fluorophore-encapsulated immunoliposomes in a microtiter plate for the rapid and automated detection of molecules with multivalent antigenic sites.-
dc.languageEnglish-
dc.titleImmunoliposomes sandwich fluorometric assay (ILSF) for detection of Escherichia coli O157:H7-
dc.typeArticle-
dc.relation.issue6-
dc.relation.volume69-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpageM151-
dc.relation.lastpageM156-
dc.relation.journaltitleJournal of Food Science-
dc.identifier.wosidWOS:000223489600021-
dc.identifier.scopusid2-s2.0-4143114591-
dc.author.googlePark S.-
dc.author.googleOh S.-
dc.author.googleDurst R.A.-
dc.contributor.scopusid박성수(9275920900;41262153700)-
dc.date.modifydate20230627101106-
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자연과학대학 > 화학·나노과학전공 > Journal papers
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