Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/55129
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dc.contributor.authorKanet Pakdeepaken_US
dc.contributor.authorSupansa Pataen_US
dc.contributor.authorSawitree Chiampanichayakulen_US
dc.contributor.authorWatchara Kasinrerken_US
dc.contributor.authorThanusak Tatuen_US
dc.date.accessioned2018-09-05T02:52:06Z-
dc.date.available2018-09-05T02:52:06Z-
dc.date.issued2016-11-01en_US
dc.identifier.issn15324230en_US
dc.identifier.issn15321819en_US
dc.identifier.other2-s2.0-84987958839en_US
dc.identifier.other10.1080/15321819.2016.1174135en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84987958839&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/55129-
dc.description.abstract© 2016 Taylor & Francis. Monoclonal antibodies against α-globin containing human Hbs, named AMS-Alpha1 and AMS-Alpha 2, were produced by the hybridoma technique using spleen cells enriched by the newly developed B lymphocyte enrichment protocol. These two monoclonal antibodies were of IgM class, reacting to only intact form of human Hbs A, A2, E, and F, which contain α-globin chain. By the indirect ELISA, the AMS-Alpha1 and AMS-Alpha 2 quantified less amount of α-globin chain containing hemoglobins in HbH disease than the SEA-α thalassemia 1 carriers and normal individuals. It was thus anticipated that these monoclonal antibodies can be used for detecting Hb Bart’s hydrops fetalis in which no α-globin chain is produced.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectHealth Professionsen_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleProduction and characterization of monoclonal antibodies against α-globin chain-containing human hemoglobins for detecting α-thalassemia diseaseen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Immunoassay and Immunochemistryen_US
article.volume37en_US
article.stream.affiliationsChiang Mai Universityen_US
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