Cloning and expression of partial japanese flounder(Paralichthys olivaceus) IgD

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dc.contributor.authorD H Choi-
dc.contributor.authorH N Jang-
dc.contributor.authorD M Ha-
dc.contributor.authorJae Wha Kim-
dc.contributor.authorC H Oh-
dc.contributor.authorS H Choi-
dc.date.accessioned2017-04-19T09:07:43Z-
dc.date.available2017-04-19T09:07:43Z-
dc.date.issued2007-
dc.identifier.issn12258687-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/7991-
dc.description.abstractThe cDNA sequence of the Japanese flounder (Paralychthys olivaceus) IgD has been previously reported (GenBank accession no. AB052658) and this was followed by the detection of IgD mRNA expression in some flounder organ tissues. However, it has not been determined whether the flounder IgD gene is virtually expressed into IgD protein. To characterize the flounder immunoglobulins utilized in elucidating the mechanism, evolution and diversity of the flounder immune system, antibodies specific to IgD and IgM were necessary. In the present study, partial flounder recombinant IgD (rIgD), IgM (rIgM) and the conserved regions of IgD and IgM (rCIg) were produced by cloning the cDNA sequence using isotype specific primers which were designed to produce unique fragments of IgD and IgM specific amino acid sequences. The production of recombinant Igs was ascertained by SDS-gel electrophoresis and immunoblot analysis using anti-T7 · Taq antibody. The produced recombinant Igs were purified using affinity columns, and used as immunogens. Antibodies specific to the isotype of flounder Igs were generated by immunizing rabbits with rfIgs and the antibodies produced were identified by enzyme-linked immunosorbent assay (ELISA) and immunoblotting. Specificities of the generated antibodies were evaluated by testing cross-reactivity between recombinant IgM and IgD. By ELISA, rabbit antibodies against the rfIgD fragment (anti-rfIgD) failed to recognize any kind of flounder serum Igs, whereas respective antibodies against rfCIg (anti-rfCIg) and rfIgM fragments (anti-rfIgM) reacted with serum Igs. Likewise, in immunoblot assays, though anti-rfIgD did not, both anti-rfCIg and anti-rfIgM bound with the ∼85 kd flounder IgM heavy chain. By flow cytometry analysis, anti-rfCIg, anti-rfIgD and anti-rfIgM reacted with 6%, 3% and 6.5% of cells, respectively, suggesting that flounder IgD is not secreted in serum but expressed on flounder B-like cell surfaces as in mammals. Antibodies produced against recombinant flounder Igs could be used to develop sandwich assay systems for detecting flounder Igs and for further investigating the flounder immune system.-
dc.publisherSouth Korea-
dc.titleCloning and expression of partial japanese flounder(Paralichthys olivaceus) IgD-
dc.title.alternativeCloning and expression of partial japanese flounder(Paralichthys olivaceus) IgD-
dc.typeArticle-
dc.citation.titleBMB Reports-
dc.citation.number4-
dc.citation.endPage466-
dc.citation.startPage459-
dc.citation.volume40-
dc.contributor.affiliatedAuthorJae Wha Kim-
dc.contributor.alternativeName최대한-
dc.contributor.alternativeName장한나-
dc.contributor.alternativeName하대망-
dc.contributor.alternativeName김재화-
dc.contributor.alternativeName오찬호-
dc.contributor.alternativeName최상훈-
dc.identifier.bibliographicCitationBMB Reports, vol. 40, no. 4, pp. 459-466-
dc.subject.keywordcDNA-
dc.subject.keywordELISA-
dc.subject.keywordflounder-
dc.subject.keywordIgD-
dc.subject.keywordrecombinant protein-
dc.subject.keywordmolecular cloning-
dc.subject.keywordcloning, molecular-
dc.subject.localcDNA-
dc.subject.localELISA-
dc.subject.localflounder-
dc.subject.localFlounder-
dc.subject.localIgD-
dc.subject.localrecombinant protein-
dc.subject.localRecombinant protein-
dc.subject.localmolecular cloning-
dc.subject.localMolecular cloning-
dc.subject.localcloning, molecular-
dc.description.journalClassY-
Appears in Collections:
Division of Biomaterials Research > Cell Factory Research Center > 1. Journal Articles
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