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Isolation and characterization of IgG molecules expressing latent group b allotypes from pedigreed b4b4 rabbits

Latent group b markers were detected in sera, in IgG preparations, and on isolated L chains from rabbits bred for homozygosity at the b locus. Serologic analysis of sera from an extended family of homozygous b4 rabbits revealed the presence of latent b allotypes in 5 of 37 sera tested. Latent b5 and...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1978
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2184954/
https://www.ncbi.nlm.nih.gov/pubmed/702048
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collection PubMed
description Latent group b markers were detected in sera, in IgG preparations, and on isolated L chains from rabbits bred for homozygosity at the b locus. Serologic analysis of sera from an extended family of homozygous b4 rabbits revealed the presence of latent b allotypes in 5 of 37 sera tested. Latent b5 and b9 markers were identified; none of the sera tested contained latent b6. In two instances, the level of latent b9 allotypes was sufficiently high to permit isolation and detailed serologic characterization of the immunoglobulin population bearing this allotype. The fact that latent allotypes were detected in pedigreed homozygous rabbits minimizes the possibility that lymphoid cell chimerism is involved in latent allotype expression. Furthermore, characterization of the b9 IgG population indicates that the latent allotypic determinants do not reside on a subset of molecules with dual allotypic reactivity.
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spelling pubmed-21849542008-04-17 Isolation and characterization of IgG molecules expressing latent group b allotypes from pedigreed b4b4 rabbits J Exp Med Articles Latent group b markers were detected in sera, in IgG preparations, and on isolated L chains from rabbits bred for homozygosity at the b locus. Serologic analysis of sera from an extended family of homozygous b4 rabbits revealed the presence of latent b allotypes in 5 of 37 sera tested. Latent b5 and b9 markers were identified; none of the sera tested contained latent b6. In two instances, the level of latent b9 allotypes was sufficiently high to permit isolation and detailed serologic characterization of the immunoglobulin population bearing this allotype. The fact that latent allotypes were detected in pedigreed homozygous rabbits minimizes the possibility that lymphoid cell chimerism is involved in latent allotype expression. Furthermore, characterization of the b9 IgG population indicates that the latent allotypic determinants do not reside on a subset of molecules with dual allotypic reactivity. The Rockefeller University Press 1978-08-01 /pmc/articles/PMC2184954/ /pubmed/702048 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Isolation and characterization of IgG molecules expressing latent group b allotypes from pedigreed b4b4 rabbits
title Isolation and characterization of IgG molecules expressing latent group b allotypes from pedigreed b4b4 rabbits
title_full Isolation and characterization of IgG molecules expressing latent group b allotypes from pedigreed b4b4 rabbits
title_fullStr Isolation and characterization of IgG molecules expressing latent group b allotypes from pedigreed b4b4 rabbits
title_full_unstemmed Isolation and characterization of IgG molecules expressing latent group b allotypes from pedigreed b4b4 rabbits
title_short Isolation and characterization of IgG molecules expressing latent group b allotypes from pedigreed b4b4 rabbits
title_sort isolation and characterization of igg molecules expressing latent group b allotypes from pedigreed b4b4 rabbits
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2184954/
https://www.ncbi.nlm.nih.gov/pubmed/702048