Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/59340
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dc.contributor.authorYaowapa Khamtaen_US
dc.contributor.authorMookda Pattarawarapanen_US
dc.contributor.authorSawitree Nangolaen_US
dc.contributor.authorChatchai Tayapiwatanaen_US
dc.date.accessioned2018-09-10T03:14:02Z-
dc.date.available2018-09-10T03:14:02Z-
dc.date.issued2009-10-01en_US
dc.identifier.issn15324230en_US
dc.identifier.issn15321819en_US
dc.identifier.other2-s2.0-70449730062en_US
dc.identifier.other10.1080/15321810903188284en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=70449730062&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/59340-
dc.description.abstractSalbutamol, one of the β-agonists, is misused as a growth promoter in meat producing animals. In-house synthesized colloidal gold was conjugated with the polyclonal anti-salbutamol antibodies. A rapid immunochromatographic assay was developed in a competitive format. The salbutamol-BSA conjugate and goat anti-rabbit IgG were immobilized on a nitrocellulose membrane as test and control lines, respectively. The color intensity of a purple test line was inversely proportional to the amount of salbutamol presenting in the samples. The sensitivity was estimated to be about 80ng/mL of salbutamol in PBS. The method can be useful as an on-site screening procedure for detection of salbutamol.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectHealth Professionsen_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleDevelopment of immunochromatographic assay for the on-site detection of salbutamolen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Immunoassay and Immunochemistryen_US
article.volume30en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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