Number of the records: 1  

Redox labelling of nucleic acids for analyzing nucleotide sequences and monitoring DNA-protein interactions

  1. 1.
    SYSNO ASEP0361621
    Document TypeC - Proceedings Paper (int. conf.)
    R&D Document TypeThe record was not marked in the RIV
    TitleRedox labelling of nucleic acids for analyzing nucleotide sequences and monitoring DNA-protein interactions
    Author(s) Fojta, Miroslav (BFU-R) RID, ORCID
    Havran, Luděk (BFU-R) RID, ORCID
    Horáková Brázdilová, Petra (BFU-R)
    Pivoňková, Hana (BFU-R) ORCID
    Kostečka, Pavel (BFU-R)
    Macíčková-Cahová, Hana (UOCHB-X) RID, ORCID
    Raindlová, Veronika (UOCHB-X) RID
    Vrábel, Milan (UOCHB-X) RID, ORCID
    Hocek, Michal (UOCHB-X) RID, ORCID
    Number of authors9
    Source TitleChemistry of Nucleic Acid Components. 15th Symposium. - Praha : Institute of Organic Chemistry and Biochemistry AS CR, v. v. i., 2011 / Hocek M. - ISBN 978-80-86241-37-1
    Pagess. 155-158
    Number of pages4 s.
    ActionChemistry of Nucleic Acid Components /15./
    Event date05.06.2011-10.06.2011
    VEvent locationČeský Krumlov
    CountryCZ - Czech Republic
    Event typeEUR
    Languageeng - English
    CountryCZ - Czech Republic
    KeywordsDNA ; electrochemistry ; redox labeling
    Subject RIVCC - Organic Chemistry
    R&D ProjectsLC512 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    LC06035 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    IAA400040901 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    IAA400040903 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    GA203/09/0317 GA ČR - Czech Science Foundation (CSF)
    GPP206/11/P739 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    CEZAV0Z40550506 - UOCHB-X (2005-2011)
    AV0Z50040507 - BFU-R (2005-2011)
    AV0Z50040702 - BFU-R (2007-2013)
    AnnotationNucleobase labelling of DNA for electrochemical sensing was attained through chemical modification of thymine bases with osmium tetroxide in the presence of nitrogenous ligands, or via enzymatic incorporation of nucleotide conjugates with redox-active moieties using labelled deoxynucleoside triphosphates. DNA hybridization, primer extension and PCR techniques were used for sequence-specific DNA assays. Tail-labelled DNA substrates were applied to monitor DNA binding by tumour suppressor p53 protein.
    WorkplaceInstitute of Organic Chemistry and Biochemistry
    Contactasep@uochb.cas.cz ; Kateřina Šperková, Tel.: 232 002 584 ; Jana Procházková, Tel.: 220 183 418
    Year of Publishing2012
Number of the records: 1  

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