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An overview of apoptosis assays detecting DNA fragmentation

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F18%3A39913187" target="_blank" >RIV/00216275:25310/18:39913187 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1007/s11033-018-4258-9" target="_blank" >http://dx.doi.org/10.1007/s11033-018-4258-9</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s11033-018-4258-9" target="_blank" >10.1007/s11033-018-4258-9</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    An overview of apoptosis assays detecting DNA fragmentation

  • Original language description

    Apoptosis has been recognized as a type of programmed cell death connected with characteristic morphological and biochemical changes in cells. This programmed cell death plays an important role in the genesis of a number of physiological and pathological processes. Thus, it can be very important to detect the signs of apoptosis in a study of cellular metabolism. The present paper provides an overview of methods often being used for detecting DNA fragmentation as one of the most specific findings in apoptosis. To date, three routine assays have been developed for detecting DNA fragmentation: DNA ladder assay, TUNEL assay, and comet assay. All these methods differ in their principles for detecting DNA fragmentation. DNA ladder assay detects the characteristic &quot;DNA ladder&quot; pattern formed during internucleosomal cleavage of DNA. Terminal deoxynUcleotidyl transferase Nick-End Labeling (TUNEL) assay detects DNA strand breaks using terminal deoxynucleotidyl transferase catalyzing attachment of modified deoxynucleotides on the DNA strand breaks. Comet assay can be used for detecting nucleus breakdown producing single/double-strand DNA breaks. The aim of this review is to describe the present knowledge on these three methods, including optimized approaches, techniques, and limitations.

  • 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

    10609 - Biochemical research methods

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2018

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Molecular Biology Reports

  • ISSN

    0301-4851

  • e-ISSN

  • Volume of the periodical

    45

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    10

  • Pages from-to

    1469-1478

  • UT code for WoS article

    000444752900076

  • EID of the result in the Scopus database

    2-s2.0-85050181397