An enzyme-linked immunoassay for the levansucrase of Zymomonas mobilis using specific antibodies produced against the cloned enzyme

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dc.contributor.authorJu Won Kwak-
dc.contributor.authorYoung Gyo Seo-
dc.contributor.authorKi Bang Song-
dc.contributor.authorSang Ki Rhee-
dc.date.accessioned2017-04-19T08:45:20Z-
dc.date.available2017-04-19T08:45:20Z-
dc.date.issued1996-
dc.identifier.issn0951-208X-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/3706-
dc.description.abstractLevansucrase gene (levU) of Z. mobilis had been cloned and overexpressed in Escherichia coli (Song, K.-B. and Rhee, S.-K. (1994) Biotechnol. Lett. 16, 1305-1310). The levansucrase was purified and specific antibodies against it were raised in rabbits. Specificity of the antibodies was demonstrated by Western analysis. By using the antibodies, an efficient, enzyme-linked immunosorbent assay (ELISA) amenable to immunochemical analysis of the levansucrase has been developed. The working range of levansucrase concentration in the developed ELISA was between 75 and 300 ng/ml. The assay was very sensitive to detect the levansucrase as little as 37 ng/ml.-
dc.publisherUnknown-
dc.titleAn enzyme-linked immunoassay for the levansucrase of Zymomonas mobilis using specific antibodies produced against the cloned enzyme-
dc.title.alternativeAn enzyme-linked immunoassay for the levansucrase of Zymomonas mobilis using specific antibodies produced against the cloned enzyme-
dc.typeArticle-
dc.citation.titleBiotechnology Techniques-
dc.citation.number2-
dc.citation.endPage132-
dc.citation.startPage127-
dc.citation.volume10-
dc.contributor.affiliatedAuthorJu Won Kwak-
dc.contributor.affiliatedAuthorYoung Gyo Seo-
dc.contributor.affiliatedAuthorKi Bang Song-
dc.contributor.affiliatedAuthorSang Ki Rhee-
dc.contributor.alternativeName곽주원-
dc.contributor.alternativeName서영교-
dc.contributor.alternativeName송기방-
dc.contributor.alternativeName이상기-
dc.identifier.bibliographicCitationBiotechnology Techniques, vol. 10, no. 2, pp. 127-132-
dc.identifier.doi10.1007/BF00765195-
dc.description.journalClassN-
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