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Generation of a novel monoclonal antibody against inflammatory biomarker S100A8 using hybridoma technology

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dc.contributor.authorKim, J.-P.-
dc.contributor.authorYun, H.-
dc.contributor.authorKim, E.-J.-
dc.contributor.authorKim, Y.-G.-
dc.contributor.authorLee, C.-S.-
dc.contributor.authorKo, B.J.-
dc.contributor.authorKim, B.-G.-
dc.contributor.authorJeong, H.-J.-
dc.date.accessioned2023-05-30T06:40:07Z-
dc.date.available2023-05-30T06:40:07Z-
dc.date.created2023-04-11-
dc.date.issued2023-06-
dc.identifier.issn0141-5492-
dc.identifier.urihttps://scholarworks.bwise.kr/ssu/handle/2018.sw.ssu/43915-
dc.description.abstractObjectives: S100A8 is highly expressed in several inflammatory and oncological conditions. To address the current lack of a reliable and sensitive detection method for S100A8, we generated a monoclonal antibody with a high binding affinity to human S100A8 to enable early disease diagnosis. Results: A soluble recombinant S100A8 protein with a high yield and purity was produced using Escherichia coli. Next, mice were immunized with recombinant S100A8 to obtain anti-human S100A8 monoclonal antibodies using hybridoma technology. Lastly, the high binding activity of the antibody was confirmed and its sequence was identified. Conclusions: This method, including the production of antigens and antibodies, will be useful for the generation of hybridoma cell lines that produce anti-S100A8 monoclonal antibodies. Moreover, the sequence information of the antibody can be used to develop a recombinant antibody for use in various research and clinical applications. © 2023, The Author(s), under exclusive licence to Springer Nature B.V.-
dc.language영어-
dc.language.isoen-
dc.publisherSpringer Science and Business Media B.V.-
dc.relation.isPartOfBiotechnology Letters-
dc.titleGeneration of a novel monoclonal antibody against inflammatory biomarker S100A8 using hybridoma technology-
dc.typeArticle-
dc.identifier.doi10.1007/s10529-023-03364-0-
dc.type.rimsART-
dc.identifier.bibliographicCitationBiotechnology Letters, v.45, no.5-6, pp.589 - 600-
dc.description.journalClass1-
dc.identifier.wosid000956847000001-
dc.identifier.scopusid2-s2.0-85151074110-
dc.citation.endPage600-
dc.citation.number5-6-
dc.citation.startPage589-
dc.citation.titleBiotechnology Letters-
dc.citation.volume45-
dc.contributor.affiliatedAuthorKim, Y.-G.-
dc.type.docTypeArticle in Press-
dc.description.isOpenAccessN-
dc.subject.keywordAuthorHybridoma technology-
dc.subject.keywordAuthorInflammation-
dc.subject.keywordAuthorMonoclonal antibody-
dc.subject.keywordAuthorMRP8-
dc.subject.keywordAuthorS100A8-
dc.subject.keywordPlusGINGIVAL CREVICULAR FLUID-
dc.subject.keywordPlusCALCIUM-BINDING PROTEINS-
dc.subject.keywordPlusMRP14-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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