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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/35533
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dc.contributor.authorNang Mo Homen_US
dc.contributor.authorChamras Promptmasen_US
dc.contributor.authorKesara Wat-Aksornen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-11-23T09:47:25Z-
dc.date.available2018-11-23T09:47:25Z-
dc.date.issued2015-01-01en_US
dc.identifier.citationAnalytical Letters. Vol.48, No.7 (2015), 1128-1138en_US
dc.identifier.issn1532236Xen_US
dc.identifier.issn00032719en_US
dc.identifier.other2-s2.0-84923310392en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84923310392&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/35533-
dc.description.abstract© 2015, Copyright © Taylor & Francis Group, LLC. A DNA sensor based on an ion sensitive field effect transistor (ISFET) with protein A modification for characterization of DNA hybridization is reported. The surface of the ISFET was modified with protein A via physical adsorption. Protein A binds specifically to the crystallizable fragment of the antibody leading to uniform orientation of the antigen binding site. In order to characterize DNA hybridization, the antibiotin antibody was immobilized to protein A and a single-strand biotinylated DNA probe was added to bind to a specific antibiotin antibody. The voltage shift of the DNA hybridization was observed after the complementary DNA target was added to the immobilized probe. The noncomplementary DNA target was also tested as a negative control. The optimal concentrations were 1 mg/mL for protein A, 1 mg/mL for the anti-biotin antibody, 0.5 µM for the biotinylated probe, and 0.5 µM for the synthetic DNA target. Nevertheless, high concentrations of protein A and antibiotin may prevent the hybridization signal detection; therefore, 0.1 mg/mL of protein A and antibiotin were employed instead of their optimal concentrations. By this strategy, DNA hybridization of the synthetic target was successfully measured with a limit of detection of approximately 0.08 µM. In addition, complementary DNA was differentiated from a noncomplementary DNA target.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84923310392&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectMedicineen_US
dc.titleDetection of DNA Hybridization Using Protein A Modified Ion Sensitive Field Effect Transistoren_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1080/00032719.2014.976871en_US
Appears in Collections:Scopus 2011-2015

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