Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/55149
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dc.contributor.authorWitida Laopajonen_US
dc.contributor.authorNuchjira Takheawen_US
dc.contributor.authorWatchara Kasinrerken_US
dc.contributor.authorSupansa Pataen_US
dc.date.accessioned2018-09-05T02:52:26Z-
dc.date.available2018-09-05T02:52:26Z-
dc.date.issued2016-09-02en_US
dc.identifier.issn15324230en_US
dc.identifier.issn15321819en_US
dc.identifier.other2-s2.0-84975512237en_US
dc.identifier.other10.1080/15321819.2016.1171780en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84975512237&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/55149-
dc.description.abstract© 2016 Taylor & Francis. The current available assays cannot differentiate the stages of phagocytosis. We, therefore, established methods for concurrent detection of antigen attachment and engulfment by phagocyte using latex beads coated with lipopolysaccharide, rabbit IgG, and carboxyfluorescein diacetate succinimidyl ester. The generated beads were incubated with whole blood at 37°C for 1 hr and stained with PE-Cy5.5 anti-rabbit IgG antibody. By flow cytometry, attachment and phagocytic processes could be detected, simultaneously. The established method is a valuable tool for diagnosis of phagocytic disorder and study of molecules involved in phagocytosis.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectHealth Professionsen_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleSimultaneous flow cytometric measurement of antigen attachment to phagocytes and phagocytosisen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Immunoassay and Immunochemistryen_US
article.volume37en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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