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Presence of matrix-specific antibodies in affinity-purified polyclonal antibodies

dc.contributor.authorSweet, Stuart C.en_US
dc.contributor.authorGnegy, Margaret E.en_US
dc.contributor.authorWelsh, Michael J.en_US
dc.date.accessioned2006-04-10T14:50:02Z
dc.date.available2006-04-10T14:50:02Z
dc.date.issued1991-01-24en_US
dc.identifier.citationSweet, Stuart C., Gnegy, Margaret E., Welsh, Michael J. (1991/01/24)."Presence of matrix-specific antibodies in affinity-purified polyclonal antibodies." Journal of Immunological Methods 136(1): 31-36. <http://hdl.handle.net/2027.42/29497>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T2Y-476MXTR-15N/2/93c0a157b2015ddb62b82a8972e74db3en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/29497
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1995710&dopt=citationen_US
dc.description.abstractIn general, antigen affinity columns made with commercially prepared activated affinity supports bind antibody specific for the coupled antigen. Nonetheless, in some cases affinity purification may yield antibodies to molecules other than the molecule of interest. In this report, we demonstrate such an occurrence: an antibody which adsorbs to an Affi-Prep 10 affinity matrix was found in the serum of sheep immunized against calmodulin. The contaminating antibody bound to cell nuclei and condensed chromosomes; the composition of the Affi-Prep 10 matrix suggests that the antibody may cross-react to the sugar-phosphate backbone of DNA. We were able to remove the contaminating antibody from the anti-calmodulin by passing the affinity-purified mixture over an antigen-free Affi-Prep 10 column.en_US
dc.format.extent483304 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titlePresence of matrix-specific antibodies in affinity-purified polyclonal antibodiesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_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 Anatomy and Cell Biology, University of Michigan Medical School, Ann Arbor, MI 48109-0616, U.S.A.en_US
dc.contributor.affiliationumDepartment of Pharmacology, University of Michigan Medical School, Ann Arbor, MI 48109-0626, U.S.A.en_US
dc.contributor.affiliationumDepartment of Anatomy and Cell Biology, University of Michigan Medical School, Ann Arbor, MI 48109-0616, U.S.A.en_US
dc.identifier.pmid1995710en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/29497/1/0000583.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0022-1759(91)90246-Cen_US
dc.identifier.sourceJournal of Immunological Methodsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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