Vinblastine determination measured by a sensitive ELISA inhibition assay = ELISA inhibition assay에 의한 Vinblastine의 측정

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dc.contributor.authorJae Wha Kim-
dc.contributor.authorMi Young Han-
dc.contributor.authorHee Gu Lee-
dc.contributor.authorEun Young Song-
dc.contributor.authorTai Wha Chung-
dc.contributor.authorKyung Soo Nam-
dc.contributor.authorIn Seong Choe-
dc.date.accessioned2017-04-19T08:45:15Z-
dc.date.available2017-04-19T08:45:15Z-
dc.date.issued1996-
dc.identifier.issnI000-0011-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/3686-
dc.description.abstractSpecific monoclonal antibodies(mAbs) against bis-indole alkaloids related to vinblastine were established to develop a simple and specific immunoassay system for the quantitation of Vinca alkaloids. Vinca alkaloids were extracted from tissue cultured cells of periwinkle plant (Vinca rosea L.). Spleen cells from Balb/c mice immunized with vinblastine-bovine serum albumin(VBL-BSA) conjugate as immunogen were fused with myeloma cells(Sp2/0-Ag.l4) in the presence of polyethylene glycol. In the preliminary experiments, 32 clones which highly reacted with VBL-BSA conjugate were selected by ELISA(Enzyme-linked immunosorbent assay). These clones were further analyzed by inhibition assay of ELISA. The results obtained with two typical monoclonal antibodies, KN-1 and KN-2, were described. KN-1 exhibited considerable reactivities with soluble dimeric bis-indole alkaloids, whereas no cross reacted with monomeric bis-indole alkaloids. However KN-2 showed cross reactivity with mono- and di-meric bis-indole alkaloids. Furthermore, KN-1 was applied to the immunoassay system for determining the VBL amounts of in vitro cultured cell extracts. This assay system could detect dimeric vinca alkaloid as low as 0.05 nM.-
dc.publisherKorea Soc-Assoc-Inst-
dc.titleVinblastine determination measured by a sensitive ELISA inhibition assay = ELISA inhibition assay에 의한 Vinblastine의 측정-
dc.title.alternativeVinblastine determination measured by a sensitive ELISA inhibition assay-
dc.typeArticle-
dc.citation.titleKorean Journal of Experimental & Biomedical Science-
dc.citation.number1-
dc.citation.endPage126-
dc.citation.startPage121-
dc.citation.volume2-
dc.contributor.affiliatedAuthorJae Wha Kim-
dc.contributor.affiliatedAuthorMi Young Han-
dc.contributor.affiliatedAuthorHee Gu Lee-
dc.contributor.affiliatedAuthorEun Young Song-
dc.contributor.affiliatedAuthorTai Wha Chung-
dc.contributor.affiliatedAuthorIn Seong Choe-
dc.contributor.alternativeName김재화-
dc.contributor.alternativeName한미영-
dc.contributor.alternativeName이희구-
dc.contributor.alternativeName송은영-
dc.contributor.alternativeName정태화-
dc.contributor.alternativeName남경수-
dc.contributor.alternativeName최인성-
dc.identifier.bibliographicCitationKorean Journal of Experimental & Biomedical Science, vol. 2, no. 1, pp. 121-126-
dc.subject.keywordVinblastine-
dc.subject.keywordEnzyme-linked immunosorbent assay(ELISA)-
dc.subject.keywordInhibition assay of ELISA.-
dc.subject.localvinblastine-
dc.subject.localVinblastine-
dc.subject.localELISA-
dc.subject.localELISA (enzyme-liked immunosorbent assay)-
dc.subject.localEnzyme-linked immunosorbent assay(ELISA)-
dc.subject.localenzyme-linked immunosorbent assay-
dc.subject.localenzyme-linked immunosorbent assay (ELISA)-
dc.subject.localInhibition assay of ELISA.-
dc.description.journalClassN-
Appears in Collections:
Division of A.I. & Biomedical Research > Immunotherapy Research Center > 1. Journal Articles
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