ARTÍCULO

The enzyme-modified comet assay: Enzyme incubation step in 2 vs 12-gels/slide systems

Autores: Muruzábal Gambarte, Damián; Langie, S, A, S.; Pourrut, B. ; Azqueta Oscoz, Amaya (Autor de correspondencia)
Título de la revista: MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS
ISSN: 1383-5718
Volumen: 845
Fecha de publicación: 2019
Lugar: WOS
Resumen:
The enzyme-modified comet assay is a commonly used method to detect specific DNA lesions. However, still a lot of errors are made by many users, leading to dubious results and even misinterpretations. This technical note describes some critical points in the use of the enzyme-modified comet assay, such as the enzyme concentration, the time of incubation, the format used and the equipment. To illustrate the importance of these conditions/ parameters, titration experiments of formamidopyrimidine DNA glycosylase (Fpg) were performed using the 2 gels/slide and the 12 minigels/slide formats (plus the 12-Gel Comet Assay Unit (TM)). Incubation times of 15 and 30 min, and 1 h were used. Results showed that the 12 minigels/slide system requires a lower volume and concentration of Fpg. A longer time of incubation has a bigger impact when using such format. Moreover, the paper describes how to perform and interpret a titration experiment when using the enzyme. modified comet assay.