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Immunological studies of the sperm-specific phosphoglycerate kinase-2 of mice

dc.contributor.authorErickson, Robert P.en_US
dc.contributor.authorHarper, Kenneth J.en_US
dc.contributor.authorMenge, Alan C.en_US
dc.contributor.authorLee, Chi-Yu Gregoryen_US
dc.date.accessioned2006-04-07T17:32:18Z
dc.date.available2006-04-07T17:32:18Z
dc.date.issued1979-10en_US
dc.identifier.citationErickson, Robert P., Harper, Kenneth, Menge, Alan, Lee, Chi-yu (1979/10)."Immunological studies of the sperm-specific phosphoglycerate kinase-2 of mice." Journal of Reproductive Immunology 1(3): 185-191. <http://hdl.handle.net/2027.42/23483>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T8W-476M29M-33/2/48423fde1cc1e83a17e04f605d81b42aen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/23483
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=551176&dopt=citationen_US
dc.description.abstractAntiserum was prepared to 500-fold purified PGK-2A from mouse testes. Despite the apparent high purity of the immunizing antigen, double diffusion analyses showed two precipitin lines, one of which can be shown to correspond to PGK-2. An immunoabsorbent column of liver homogenate coupled to cyanogen bromide-activated Sepharose was used to remove the contaminating antibody. Both immuno-inactivation and double diffusion analyses demonstrated that the PGK-2 antigen appeared in testes between days 30 and 34 of postnatal development. The antisera prepared against highly purified PGK-2A did not disclose any immunological differences between PGK-2A, PGK-2B, and PGK-2C either by double diffusion analyses or quantitative immunoprecipitation. Antisera to PGK-2 did not inhibit in vitro fertilization of zona-free hamster ova by mouse spermatozoa.en_US
dc.format.extent558322 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleImmunological studies of the sperm-specific phosphoglycerate kinase-2 of miceen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelObstetrics and Gynecologyen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan School of Medicine, Ann Arbor, MI 48109, USA;Department of Pediatrics, University of Michigan School of Medicine, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan School of Medicine, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumDepartment of Obstetrics and Gynecology, University of Michigan School of Medicine, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationotherLaboratories of Environmental Mutagenesis and Biochemical Genetics, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, U.S.A.en_US
dc.identifier.pmid551176en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/23483/1/0000436.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0165-0378(79)90019-6en_US
dc.identifier.sourceJournal of Reproductive Immunologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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