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dc.contributor.authorBlackledge, George
dc.contributor.authorVose, Brent M
dc.contributor.authorMorris, Andrew J
dc.contributor.authorCrowther, Derek
dc.contributor.authorGallagher, John T
dc.date.accessioned2011-03-22T16:56:34Z
dc.date.available2011-03-22T16:56:34Z
dc.date.issued1982-10-15
dc.identifier.citationFlow cytometric analysis of lectin binding to human peripheral blood lymphocytes. 1982, 208 (1):69-75 Biochem Jen
dc.identifier.issn0264-6021
dc.identifier.pmid6818949
dc.identifier.urihttp://hdl.handle.net/10541/125354
dc.description.abstractThe binding of fluorescein-conjugated lentil lectin and concanavalin A to the surface membrane of human peripheral blood lymphocytes was studied by flow cytometry. The lymphocytes bound 3-fold more lentil lectin molecules compared with concanavalin A molecules and lentil lectin binding approached saturation at a much lower concentration than did that of concanavalin A. Lentil lectin identified two groups of lymphocytes: a low-binding T-cell fraction and a high-binding B-cell-enriched fraction. Concanavalin A did not discriminate between these populations in unseparated lymphocytes. Competition studies indicated that lentil lectin and concanavalin A were bound to different sites on the lymphocyte surface, although about 50% of lentil lectin sites were in close proximity to concanavalin A sites.
dc.language.isoenen
dc.subject.meshAdult
dc.subject.meshCell Membrane
dc.subject.meshCell Separation
dc.subject.meshConcanavalin A
dc.subject.meshFlow Cytometry
dc.subject.meshFluorescein-5-isothiocyanate
dc.subject.meshFluoresceins
dc.subject.meshFluorescent Dyes
dc.subject.meshHumans
dc.subject.meshLectins
dc.subject.meshLymphocytes
dc.subject.meshReceptors, Mitogen
dc.subject.meshRosette Formation
dc.subject.meshThiocyanates
dc.titleFlow cytometric analysis of lectin binding to human peripheral blood lymphocytes.en
dc.typeArticleen
dc.contributor.departmentCancer Research Campaign, Department of Medical Oncology, Christie Hospital and Holt Radium Institute, UK.en
dc.identifier.journalThe Biochemical Journalen
html.description.abstractThe binding of fluorescein-conjugated lentil lectin and concanavalin A to the surface membrane of human peripheral blood lymphocytes was studied by flow cytometry. The lymphocytes bound 3-fold more lentil lectin molecules compared with concanavalin A molecules and lentil lectin binding approached saturation at a much lower concentration than did that of concanavalin A. Lentil lectin identified two groups of lymphocytes: a low-binding T-cell fraction and a high-binding B-cell-enriched fraction. Concanavalin A did not discriminate between these populations in unseparated lymphocytes. Competition studies indicated that lentil lectin and concanavalin A were bound to different sites on the lymphocyte surface, although about 50% of lentil lectin sites were in close proximity to concanavalin A sites.


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