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ASTM E 2186 REV A Document Information:
Title
Standard Guide for Determining DNA Single-Strand Damage in Eukaryotic Cells Using the Comet Assay
ASTM International
Publication Date:
Apr 10, 2002
Scope:
This guide covers the recommended criteria for performing a
single-cell gel electrophoresis assay
(SCG) or Comet assay for the measurement of DNA single-strand breaks
in eukaryotic cells. The Comet
assay is a very sensitive method for detecting strand breaks in the
DNA of individual cells. The
majority of studies utilizing the Comet assay have focused on medical
applications and have
therefore examined DNA damage in mammalian cells in vitro and in vivo
(1-4). There is increasing
interest in applying this assay to DNA damage in freshwater and marine
organisms to explore the
environmental implications of DNA damage.
The Comet assay has been used to screen the genotoxicity of a variety
of compounds on cells in
vitro and in vivo (5-7), as well as to evaluate the dose-dependent
anti-oxidant (protective)
properties of various compounds (3, 8-11). Using this method,
significantly elevated levels of DNA
damage have been reported in cells collected from organisms at
polluted sites compared to reference
sites (12-15). Studies have also found that increases in cellular DNA
damage correspond with higher
order effects such as decreased growth, survival, and development, and
correlate with significant
increases in contaminant body burdens (13, 16).
This guide presents protocols that facilitate the expression of DNA
alkaline labile single-strand
breaks and the determination of their abundance relative to control or
reference cells. The guide
is a general one meant to familiarize lab personnel with the basic
requirements and considerations
necessary to perform the Comet assay. It does not contain procedures
for available variants of this
assay, which allow the determination of non-alkaline labile
single-strand breaks or double-stranded
DNA strand breaks (8), distinction between different cell types (13),
identification of cells
undergoing apoptosis (programmed cell death, (1, 17)), measurement of
cellular DNA repair rates
(10), detection of the presence of photoactive DNA damaging compounds
(14), or detection of
specific DNA lesions (3, 18).
This standard does not purport to address all of the safety concerns,
if any, associated with its
use. It is the responsibility of the user of this standard to
establish appropriate safety and
health practices and determine the applicability of regulatory
requirements prior to use.
This guide is arranged as follows:
Keywords:
- biomarker
- cellular
- Comet assay
- DNA damage
- DNA strand breaks
- stress effects
- toxic
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