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Genetic variation in the carbonic anhydrase isozymes of macaque monkeys. I. The radioimmunosorbent assay
dc.contributor.authorTashian, Richard E.en_US
dc.contributor.authorMagid, Eriken_US
dc.contributor.authorDeSimone, Josephen_US
dc.date.accessioned2006-09-11T14:24:09Z
dc.date.available2006-09-11T14:24:09Z
dc.date.issued1973-02en_US
dc.identifier.citationMagid, Erik; DeSimone, Joseph; Tashian, Richard E.; (1973). "Genetic variation in the carbonic anhydrase isozymes of macaque monkeys. I. The radioimmunosorbent assay." Biochemical Genetics 8(2): 157-164. <http://hdl.handle.net/2027.42/44181>en_US
dc.identifier.issn1573-4927en_US
dc.identifier.issn0006-2928en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/44181
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=4632295&dopt=citationen_US
dc.description.abstractA radioimmunosorbent technique is described which is capable of independently detecting both isozymes of carbonic anhydrase, CA I and CA II, in concentrations as low as 1 ng/ml. The technique is used to quantitate the different electrophoretic variants of red cell CA I as well as levels of CA II in the pig-tailed macaque, Macaca nemestrina .en_US
dc.format.extent373987 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers-Plenum Publishers; Plenum Publishing Corporation ; Springer Science+Business Mediaen_US
dc.subject.otherBiochemistry, Generalen_US
dc.subject.otherBiomedicineen_US
dc.subject.otherHuman Geneticsen_US
dc.subject.otherMedical Microbiologyen_US
dc.subject.otherZoologyen_US
dc.titleGenetic variation in the carbonic anhydrase isozymes of macaque monkeys. I. The radioimmunosorbent assayen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelEcology and Evolutionary Biologyen_US
dc.subject.hlbsecondlevelNatural Resources and Environmenten_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan Medical School, Ann Arbor, Michigan; Department of Clinical Chemistry, Bispebjerg Hospital, Bispebjerg Bakke 23, 2400, Copenhagen NV, Denmarken_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan Medical School, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan Medical School, Ann Arbor, Michiganen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid4632295en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/44181/1/10528_2004_Article_BF00485543.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00485543en_US
dc.identifier.sourceBiochemical Geneticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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