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A radioimmunoassay for quantifying carbonic anhydrase isozymes in crude lysates

dc.contributor.authorTashian, Richard E.en_US
dc.contributor.authorHeadings, Verle E.en_US
dc.date.accessioned2006-09-11T14:22:51Z
dc.date.available2006-09-11T14:22:51Z
dc.date.issued1970-04en_US
dc.identifier.citationHeadings, Verle E.; Tashian, Richard E.; (1970). "A radioimmunoassay for quantifying carbonic anhydrase isozymes in crude lysates." Biochemical Genetics 4(2): 285-295. <http://hdl.handle.net/2027.42/44165>en_US
dc.identifier.issn0006-2928en_US
dc.identifier.issn1573-4927en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/44165
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=4987444&dopt=citationen_US
dc.description.abstractA radioimmunoassay was developed for quantifying each of the two genetically distinct forms of primate carbonic anhydrase, carbonic anhydrases I and II, in unpurified lysates. Under the given experimental conditions, the assay is capable of detecting a minimum of 0.025 μg of carbonic anhydrase I and 0.005 μg of carbonic anhydrase II. There is approximately 98% reproducibility upon repeated assays of a given hemolysate.en_US
dc.format.extent564921 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.otherMedical Microbiologyen_US
dc.subject.otherBiomedicineen_US
dc.subject.otherHuman Geneticsen_US
dc.subject.otherBiochemistry, Generalen_US
dc.subject.otherZoologyen_US
dc.titleA radioimmunoassay for quantifying carbonic anhydrase isozymes in crude lysatesen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelNatural Resources and Environmenten_US
dc.subject.hlbsecondlevelEcology and Evolutionary Biologyen_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; Medical Genetics Unit, Howard University College of Medicine, Box 101, Washington, D.C.en_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan Medical School, Ann Arbor, Michiganen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid4987444en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/44165/1/10528_2004_Article_BF00485779.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00485779en_US
dc.identifier.sourceBiochemical Geneticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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