Number of the records: 1  

Application of Fӧrster resonance energy transfer (FRET) for a detection of DNA mutations

  1. 1.
    SYSNO ASEP0437861
    Document TypeA - Abstract
    R&D Document TypeThe record was not marked in the RIV
    R&D Document TypeNení vybrán druh dokumentu
    TitleApplication of Fӧrster resonance energy transfer (FRET) for a detection of DNA mutations
    Author(s) Datinská, Vladimíra (UIACH-O)
    Klepárník, Karel (UIACH-O) RID, ORCID
    Belšánová, Barbora (UIACH-O)
    Minárik, M. (CZ)
    Foret, František (UIACH-O) RID, ORCID
    Number of authors5
    Source TitleITP & LACE 2014. Book of Abstracts. - : Grupo VLS Print Solution, 2014 / Guzman N. A. ; Taveres M. F. M.
    S. 93-93
    Number of pages1 s.
    Publication formOnline - E
    ActionInternational Symposium on Electro- and Liquid Phase-Separation Techniques /21./ and Latin-American Symposium on Biotechnology, Biomedical, Biopharmaceutical, and Industrial Applications of Capillary Electrophoresis and Microchip Technology /21./
    Event date04.10.2014-08.10.2014
    VEvent locationNatal
    CountryBR - Brazil
    Event typeWRD
    Languageeng - English
    CountryBR - Brazil
    Keywordsquantum dots ; Förster resonance energy transfer ; CE-LIF
    Subject RIVCB - Analytical Chemistry, Separation
    R&D ProjectsGA14-28254S GA ČR - Czech Science Foundation (CSF)
    TA02010672 GA TA ČR - Technology Agency of the Czech Republic (TA ČR)
    Institutional supportUIACH-O - RVO:68081715
    AnnotationWe have synthesized a probe consisting of CdTe QDs conjugated with oligonucleotide to be used as a donor. Conjugation reaction between carboxylated QDs and aminated oligonucleotides has been performed via zero-length cross-linkers. Sample consisting of clinically-relevant PCR amplicons labelled with ROX (6-carboxyrhodamine) served as acceptor. Upon mutation-specific sample-probe hybridization an increase in fluorescence intensity at 610 nm (the emission spectra maximum of ROX) confirmed a proper function of FRET at a presence of detected mutation. The limit of detection evaluated for PCR amplified fragments of the sample is 4x10-9 M.
    WorkplaceInstitute of Analytical Chemistry
    ContactIveta Drobníková, drobnikova@iach.cz, Tel.: 532 290 234
    Year of Publishing2015
Number of the records: 1  

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