An optimized comet-based in vitro DNA repair assay to assess base and nucleotide excision repair activity

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11120%2F20%3A43920783" target="_blank" >RIV/00216208:11120/20:43920783 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/68378041:_____/20:00552828

Výsledek na webu

<a href="https://doi.org/10.1038/s41596-020-0401-x" target="_blank" >https://doi.org/10.1038/s41596-020-0401-x</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1038/s41596-020-0401-x" target="_blank" >10.1038/s41596-020-0401-x</a>

Jazyk výsledku

angličtina

Název v původním jazyce

An optimized comet-based in vitro DNA repair assay to assess base and nucleotide excision repair activity

Popis výsledku v původním jazyce

This optimized protocol (including links to instruction videos) describes a comet-based in vitro DNA repair assay that is relatively simple, versatile, and inexpensive, enabling the detection of base and nucleotide excision repair activity. Protein extracts from samples are incubated with agarose-embedded substrate nucleoids (&apos;naked&apos; supercoiled DNA) containing specifically induced DNA lesions (e.g., resulting from oxidation, UVC radiation or benzo[a]pyrene-diol epoxide treatment). DNA incisions produced during the incubation reaction are quantified as strand breaks after electrophoresis, reflecting the extract&apos;s incision activity. The method has been applied in cell culture model systems, human biomonitoring and clinical investigations, and animal studies, using isolated blood cells and various solid tissues. Once extracts and substrates are prepared, the assay can be completed within 2 d.

Název v anglickém jazyce

An optimized comet-based in vitro DNA repair assay to assess base and nucleotide excision repair activity

Popis výsledku anglicky

This optimized protocol (including links to instruction videos) describes a comet-based in vitro DNA repair assay that is relatively simple, versatile, and inexpensive, enabling the detection of base and nucleotide excision repair activity. Protein extracts from samples are incubated with agarose-embedded substrate nucleoids (&apos;naked&apos; supercoiled DNA) containing specifically induced DNA lesions (e.g., resulting from oxidation, UVC radiation or benzo[a]pyrene-diol epoxide treatment). DNA incisions produced during the incubation reaction are quantified as strand breaks after electrophoresis, reflecting the extract&apos;s incision activity. The method has been applied in cell culture model systems, human biomonitoring and clinical investigations, and animal studies, using isolated blood cells and various solid tissues. Once extracts and substrates are prepared, the assay can be completed within 2 d.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10603 - Genetics and heredity (medical genetics to be 3)

Projekt

<a href="/cs/project/GA19-10543S" target="_blank" >GA19-10543S: Změny DNA reparačního systému související s odpovědí na léčbu ovariálního karcinomu.</a><br>

Návaznosti

V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Rok uplatnění

2020

Kód důvěrnosti údajů

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

Název periodika

Nature Protocols

ISSN

1754-2189

e-ISSN

—

Svazek periodika

15

Číslo periodika v rámci svazku

12

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

35

Strana od-do

3844-3878

Kód UT WoS článku

000590016600002

EID výsledku v databázi Scopus

2-s2.0-85096054339