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pubmed-article:2450130pubmed:abstractTextThe C region of human lambda L chains is specified by multiple C lambda genes of which three--C lambda 1, C lambda 2, and C lambda 3--encode for the isotypes designated Mcg+, Kern- Oz-, and Kern- Oz+, respectively. The Mcg, Kern, and Oz factors have been characterized by sequence differences involving specific C lambda amino acid residues. They have also been recognized serologically by polyclonal antisera but, with rare exception, these reagents are no longer available. We have obtained two murine anti-human lambda-chain mAb, 14G1 and 14D1, that recognize antigenic determinants specific for the C lambda isotypes Mcg and Oz, respectively. These antisera have been used to classify as Mcg+/Mcg- or Oz+/Oz- monoclonal lambda-chains (Bence Jones proteins) and intact Ig lambda proteins. There was complete concordance between the chemical and serologic assignment of lambda-chains as Mcg+/Mcg- or as Oz+/Oz-; no single protein expressed both isotypes. There was no evident association between the C region isotype Mcg or Oz and the V region subgroup of the protein tested. However, our finding that four of seven amyloid-associated lambda VI Bence Jones proteins were Oz+ suggests a predominant expression of the C lambda 3 gene product among proteins of this uncommon V lambda subgroup.lld:pubmed
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pubmed-article:2450130pubmed:pagination1600-4lld:pubmed
pubmed-article:2450130pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:2450130pubmed:articleTitleImmunogenic and antigenic epitopes of Ig. XXV. Monoclonal antibodies that differentiate the Mcg+/Mcg- and Oz+/Oz- C region isotypes of human lambda L chains.lld:pubmed
pubmed-article:2450130pubmed:affiliationDepartment of Immunology, University of Birmingham Medical School, England.lld:pubmed
pubmed-article:2450130pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:2450130pubmed:publicationTypeComparative Studylld:pubmed
pubmed-article:2450130pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:2450130pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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