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dc.contributor.authorShakil, T.
dc.contributor.authorRichardson, M. K.
dc.contributor.authorWaldron, E.E.
dc.contributor.authorConde, Gillian
dc.contributor.authorWood, S.
dc.contributor.authorBland, Y.
dc.contributor.authorReynolds, Gary
dc.contributor.authorMurray, Paul G.
dc.contributor.authorNelson, Paul N.
dc.date.accessioned2008-06-20T10:39:53Z
dc.date.available2008-06-20T10:39:53Z
dc.date.issued2001
dc.identifier.citationHybridoma, 20(3): 199-203
dc.identifier.issn0272-457X
dc.identifier.pmid11461669
dc.identifier.doi10.1089/027245701750293538
dc.identifier.urihttp://hdl.handle.net/2436/30255
dc.description.abstractThe generation of monoclonal antibodies (MAbs) specific for quail neural crest may provide valuable tools for studying the differentiation of embryonic precursor cells. Unfortunately, relatively few antibodies are available because of the difficulty in obtaining sufficient cells for in vivo immunization strategies. We have overcome this problem by using intrasplenic immunization with formaldehyde-fixed cells harvested from neural crest cultures. In addition, booster injections of cultured whole-embryo cells were administered intraperitoneally. Following two fusions, a total of 18 hybridomas were generated with antibody reactivity to the cytoplasm of neural crest cells. Furthermore, 32 were reactive against both somite (a noncrest mesodermal control) and crest cultures, whilst 15 were not reactive. Out of those hybridomas reactive with neural crest, six designated 160D, 164D, OE, 12E, 120E and 124E were further characterized. Interestingly MAb supernatants OE, 12E, 120E, and 124E exhibited reactivity against some but not all neural crest cells suggesting that they might recognise subpopulations. Immunoglobulin isotyping of supernatants revealed that 4 (160D, 164D, OE, and 120E) were IgM and 2 (12E and 124E) were IgG(2b). On assessing their reactivity against human tissue sections, all six hybridoma supernatants cross-reacted with neuroendocrine cells within appendix, colon and rectum. These MAbs could provide novel reagents for the understanding of neural crest development.
dc.language.isoen
dc.publisherNew Rochelle (NY): Mary Ann Liebert, Inc.
dc.relation.urlhttp://direct.bl.uk/bld/PlaceOrder.do?UIN=098727917&ETOC=RN&from=searchenginehttp://www.liebertonline.com/doi/abs/10.1089/027245701750293538?journalCode=hyb.1
dc.subjectMonoclonal antibodies
dc.subjectHybridomas
dc.subjectOncology
dc.subjectMolecular Biology
dc.subject.meshAnimals
dc.subject.meshAntibodies, Monoclonal
dc.subject.meshAntibody Specificity
dc.subject.meshHumans
dc.subject.meshMice
dc.subject.meshNeural Crest
dc.titleGeneration and characterization of monoclonal antibodies to the neural crest.
dc.typeJournal article
dc.identifier.journalHybridoma
html.description.abstractThe generation of monoclonal antibodies (MAbs) specific for quail neural crest may provide valuable tools for studying the differentiation of embryonic precursor cells. Unfortunately, relatively few antibodies are available because of the difficulty in obtaining sufficient cells for in vivo immunization strategies. We have overcome this problem by using intrasplenic immunization with formaldehyde-fixed cells harvested from neural crest cultures. In addition, booster injections of cultured whole-embryo cells were administered intraperitoneally. Following two fusions, a total of 18 hybridomas were generated with antibody reactivity to the cytoplasm of neural crest cells. Furthermore, 32 were reactive against both somite (a noncrest mesodermal control) and crest cultures, whilst 15 were not reactive. Out of those hybridomas reactive with neural crest, six designated 160D, 164D, OE, 12E, 120E and 124E were further characterized. Interestingly MAb supernatants OE, 12E, 120E, and 124E exhibited reactivity against some but not all neural crest cells suggesting that they might recognise subpopulations. Immunoglobulin isotyping of supernatants revealed that 4 (160D, 164D, OE, and 120E) were IgM and 2 (12E and 124E) were IgG(2b). On assessing their reactivity against human tissue sections, all six hybridoma supernatants cross-reacted with neuroendocrine cells within appendix, colon and rectum. These MAbs could provide novel reagents for the understanding of neural crest development.


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