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The cell free synthesis of bovine lutropin [beta] subunit

dc.contributor.authorLandefeld, Thomas D.en_US
dc.contributor.authorKepa, Jadwigaen_US
dc.date.accessioned2006-04-07T17:31:51Z
dc.date.available2006-04-07T17:31:51Z
dc.date.issued1979-10-29en_US
dc.identifier.citationLandefeld, Thomas D., Kepa, Jadwiga (1979/10/29)."The cell free synthesis of bovine lutropin [beta] subunit." Biochemical and Biophysical Research Communications 90(4): 1111-1118. <http://hdl.handle.net/2027.42/23468>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WBK-4DYN48C-FV/2/bd22a9f47756dc321ada4e98fd7e50f7en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/23468
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=518586&dopt=citationen_US
dc.description.abstractRNA prepared from bovine pituitary glands directs the synthesis of trichloroacetic acid-insoluble proteins in the wheat germ cell-free system. Antisera specific to bovine lutropin (LH) beta subunit precipitated a product with a molecular weight of approximately 17,000, suggesting a precursor. Its specificity was demonstrated by the failure of antisera to other pituitary hormones, including LH alpha and thyrotropin (TSH) beta, to successfully precipitate it and also by its competition with unlabeled LH [beta] for the beta antisera. The addition of microsomal membranes resulted in the partial processing of this 17,000 dalton protein to a product of higher molecular weight (Mr~ 19,000), suggesting glycosylation.en_US
dc.format.extent1165552 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleThe cell free synthesis of bovine lutropin [beta] subuniten_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelNatural Resources and Environmenten_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_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 Pathology Reproductive Endocrinology Program University of Michigan, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumDepartment of Pathology Reproductive Endocrinology Program University of Michigan, Ann Arbor, Michigan 48109, USAen_US
dc.identifier.pmid518586en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/23468/1/0000420.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0006-291X(79)91150-1en_US
dc.identifier.sourceBiochemical and Biophysical Research Communicationsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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