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Fast enzyme-linked electrochemical sensing of DNA hybridization at pencil graphite electrodes. Application to detect gene deletion in a human cell culture

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68081707%3A_____%2F20%3A00524530" target="_blank" >RIV/68081707:_____/20:00524530 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216224:14740/20:00118310

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S157266572030134X?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S157266572030134X?via%3Dihub</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jelechem.2020.113951" target="_blank" >10.1016/j.jelechem.2020.113951</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Fast enzyme-linked electrochemical sensing of DNA hybridization at pencil graphite electrodes. Application to detect gene deletion in a human cell culture

  • Original language description

    In this paper we present a rapid electrochemical enzyme-linked DNA hybridization assay using disposable pencil graphite electrodes (PeGE) to detect target DNA (tDNA) sequences in DNA fragments amplified by polymerase chain reaction. The procedure consists of several short (1-2 min) incubation steps, including adsorption of the tDNA at unpretreated PeGE from denaturing medium, surface blocking with milk proteins, hybridization with a biotinylated oligonucleotide probe and binding of streptavidin-alkaline phosphatase conjugate to the biotin tags. Then the PeGE is transferred into background electrolyte solution containing 1-naphthyl phosphate, which is enzymatically dephosphorylated to give electrochemically oxidizable indicator 1-naphthol. The assay, which can be performed within 7-8 min, offers a perfect discrimination between specific and nonspecific DNA amplicons and easy detection of about similar to 40 femtomoles of tDNA in large excesses of non-complementary DNA. An application on the detection of p53 gene deletion in a human cell culture, featuring a real biologicalmodel, is presented. The designed setup has a potential to be applied as one of simple, fast, robust ultralow cost do-it-yourself instruments recently introduced as diagnostic tools for third world countries. (c) 2020 Elsevier B.V. All rights reserved.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10405 - Electrochemistry (dry cells, batteries, fuel cells, corrosion metals, electrolysis)

Result continuities

  • Project

    <a href="/en/project/GAP206%2F11%2F1638" target="_blank" >GAP206/11/1638: Novel electrochemical sensors and sensing techniques for the analysis of nucleic acids structure and interactions</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2020

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Electroanalytical Chemistry

  • ISSN

    1572-6657

  • e-ISSN

  • Volume of the periodical

    862

  • Issue of the periodical within the volume

    APR 1 2020

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    7

  • Pages from-to

    113951

  • UT code for WoS article

    000525903900004

  • EID of the result in the Scopus database

    2-s2.0-85080093599