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Partial characterization of Ia antigens from murine lymphoid cells

dc.contributor.authorVitetta, Ellen S.en_US
dc.contributor.authorKlein, Janen_US
dc.contributor.authorUhr, Jonathan W.en_US
dc.date.accessioned2006-09-11T18:07:58Z
dc.date.available2006-09-11T18:07:58Z
dc.date.issued1974-12en_US
dc.identifier.citationVitetta, Ellen S.; Klein, Jan; Uhr, Jonathan W.; (1974). "Partial characterization of Ia antigens from murine lymphoid cells." Immunogenetics 1(1): 82-90. <http://hdl.handle.net/2027.42/46728>en_US
dc.identifier.issn1432-1211en_US
dc.identifier.issn0093-7711en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/46728
dc.description.abstractCongenic anti-Ia antisera were used to bind radiolabelled Ia antigens from cells of various strains of mice of known H-2 haplotype. The results indicate that Ia antigens are proteins of molecular weight 30,000 to 35,000 daltons. The Ia antigens are distinct from known H-2 antigens as judged by independent immunoprecipitation as well as by molecular weight. Ia antigens are synthesized by, and are present on the surface of lymphoid cells as evidenced by incorporation studies using 3 H-leucine and enzymatic radioiodination of cells, respectively. Tissue distribution of cell surface Ia suggests that Ia antigens are on B cells. Ia antigens were detected in the incubation media of 3 H-leucine labeled splenocytes suggesting that antigens may be secreted.en_US
dc.format.extent438952 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlag; Springer-Verlag New York Inc.en_US
dc.subject.otherCell Biologyen_US
dc.subject.otherBiomedicineen_US
dc.subject.otherImmunologyen_US
dc.subject.otherAllergologyen_US
dc.titlePartial characterization of Ia antigens from murine lymphoid cellsen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Microbiology, University of Texas, Southwestern Medical School, 75235, Dallas, Texas; Irvington House Institute and Department of Microbiology, N.Y.U. School of Medicine, 10016, New York, N.Y.; Departments of Human Genetics and Oral Biology, Schools of Dentistry and Medicine, University of Michigan, 48104, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Microbiology, University of Texas, Southwestern Medical School, 75235, Dallas, Texas; Irvington House Institute and Department of Microbiology, N.Y.U. School of Medicine, 10016, New York, N.Y.; Departments of Human Genetics and Oral Biology, Schools of Dentistry and Medicine, University of Michigan, 48104, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Microbiology, University of Texas, Southwestern Medical School, 75235, Dallas, Texas; Irvington House Institute and Department of Microbiology, N.Y.U. School of Medicine, 10016, New York, N.Y.; Departments of Human Genetics and Oral Biology, Schools of Dentistry and Medicine, University of Michigan, 48104, Ann Arbor, Michiganen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/46728/1/251_2005_Article_BF01564048.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF01564048en_US
dc.identifier.sourceImmunogeneticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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