Dna Damage Quantitation by Alkaline Gel Electrophoresis.
From: Biology Department, Brookhaven National Laboratory, Upton, NY, USA.
Methods in molecular biology (Clifton, N.J.)
- Publish Date: 2006
- ISSN: 1064-3745
- Volume: 314
- Issue:
- Pages: 251-73
- Medium: Print
- Language: English
- Citation (JAMA): Sutherland Betsy M, Bennett Paula V, Sutherland John C, et al. Dna Damage Quantitation by Alkaline Gel Electrophoresis.. Methods Mol. Biol. 2006;314:251-73
Abstract
Quantifying DNA lesions provides a powerful way to assess the level of endogenous damage or the damage level induced by radiation, chemical or other agents, as well as the ability of cells to repair such damages. Quantitative gel electrophoresis of experimental DNAs along with DNA length standards, imaging the resulting dispersed DNA and calculating the population average length allows accurate measurement of lesion frequencies. Number average length analysis provides high sensitivity and does not require any specific distribution of lesions within the DNA molecules. These methods are readily applicable to strand breaks and ultraviolet radiation induced pyrimidine dimers, but can also be used-with appropriate modifications-for ionizing radiation-induced lesions such as oxidized bases and abasic sites.
Mesh Headings (Keywords): Animals, Cells, Cultured, Comet Assay, DNA, DNA Damage, Electrophoresis, Agar Gel, Humans, Pyrimidine Dimers, Ultraviolet Rays
Check for Full Text / PubMed Unique Identifier (PMID): 16673887
This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.
Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.
The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.
