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Method Article

Comet Assay for DNA Damage Detection in Cells

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July 8th, 2025

In This Article

Abstract

Source: Ji, Y., et al. A High-Throughput Comet Assay Approach for Assessing Cellular DNA Damage. J. Vis. Exp. (2022).

The video demonstrates the comet assay for detecting DNA damage following exposure to harmful agents. Under alkaline conditions, the DNA unwinds and denatures, and upon electrophoresis, the undamaged and damaged DNA migrate differently in the agarose gel, forming a comet-shaped structure. The slowly migrating undamaged DNA forms the circular comet head, while the rapidly migrating damaged DNA fragments form the elongated comet tail.

Protocol

1. Preparation of materials for the comet assay

  1. Preparation of the microscope slides
    1. Pour 1% (w/v) normal melting point agarose [dissolved in double-distilled water (ddH2O)] in a 50 mL tube and microwave to dissolve the agarose in the ddH2O. Store at 37 °C to prevent solidification prior to coating slides. Should solidification occur, discard and prepare fresh.
    2. Pre-coat microscope slides by dipping the slides into the 50 mL tube containing 1% (w/v) normal melting point agarose.
    3. Wipe the back of the slides quickly after dipping the slides.
      NOTE: Failure to wipe the back of....

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Results

Chromatography diagram and setup for protein separation using glass plates in electrophoresis.
Figure 1: Representative images of a comet assay slide and HTP rack (microscope slide carrier). (A) For correct orientation, the pre-coated face of the microscope slide is recognized by a black dot in the right-hand corner of a microscope slide. (B) The image.......

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Disclosures

No conflicts of interest declared.

Materials

List of materials used in this article
NameCompanyCatalog NumberComments
22 x 22 mm glass coverslipsFisher Scientific, Hampton, NH, USA631-0124
Fluorescence microscope equipped<br/> &nbsp;with a cameraZeiss, Jena, Germany
HTP Comet Assay systemCleaver ScientificCOMPAC- 50
Human Keratinocyte (HaCaTs)American Type Culture Collection<br/> &nbsp;(ATCC), Manassas, VA, USADiscontinuedCan be purchased from another<br/> &nbsp;company<br/> &nbsp;ADDEXBIO TECHNOLOGIES<br/> &nbsp;Cat# T0020001
Hydrogen peroxide (H2O2)<br/> &nbsp;30% in waterFisher Scientific, Hampton, NH, USABP2633-500
Image and Data Analysis softwarePerceptive Instrument,<br/> &nbsp;Bury St Edmunds, England,<br/> &nbsp;UK125525Free image analysis softwared is<br/> &nbsp;available e.g., ImageJ
Low melting point AgaroseInvitrogen<br/> &nbsp;Waltham, MA, USAP4864
Na2 EDTA (disodium<br/> &nbsp;ethylenediaminetetraacetic acid)Sigma Aldrich,<br/> &nbsp;St. Louis, MO,<br/> &nbsp;USAE5134
NaCl (Sodium chloride)Sigma Aldrich,<br/> &nbsp;St. Louis, MO,<br/> &nbsp;USAS7653
Nanopure Infinity Ultrapure Water<br/> &nbsp;System (Barnstead Nanopure)Thermo Scientific,<br/> &nbsp;Waltham, MA,<br/> &nbsp;USAD11901Ultrapure water (16 M&Omega; cm^{-1} )
NaOH (sodium Hydroxide)Sigma Aldrich,<br/> &nbsp;St. Louis, MO, USAE5134
Normal melting point AgaroseFisher Scientific,<br/> &nbsp;Hampton, NH, USA16520100For pre-coating slides
Propidium Iodide<br/> &nbsp;(1.0 mg/mL in water)Sigma Aldrich,<br/> &nbsp;St. Louis, MO,<br/> &nbsp;USA12-541BP486410ML
Single-frosted glass microscope<br/> &nbsp;slidesFisher Scientific,<br/> &nbsp;Hampton, NH, USA12-541B
Slide boxFisher Scientific,<br/> &nbsp;Hampton, NH, USA03-448-2Light proof, to protect cells from<br/> &nbsp;the formation adventitious damage<br/> &nbsp;(according to the widely held view)<br/> &nbsp;and prevent fading of the fluorescent<br/> &nbsp;dye
Slide Chilling plateCleaver Scientific,<br/> &nbsp;Rugby, England,<br/> &nbsp;UKCSL-CHILLPLATE
Treatment dishCleaver Scientific,<br/> &nbsp;Rugby, England,<br/> &nbsp;UKSTAINDISH4X
Tris-baseSigma Aldrich,<br/> &nbsp;St. Louis, MO,<br/> &nbsp;USA93362
Triton X-100Fisher Scientific,<br/> &nbsp;Hampton, NH, USABP151-500
Trypsin EDTA (0.5%)Invitrogen<br/> &nbsp;Gibco,<br/> &nbsp;Waltham, MA, USA15400054
Vertical Slide CarrierCleaver Scientific,<br/> &nbsp;Rugby, England,<br/> &nbsp;UKCOMPAC-25

Tags

Alkaline ElectrophoresisLow Melting Point AgaroseFluorescence MicroscopyPropidium Iodide StainingNucleoid Body FormationSingle Cell SuspensionLysis Buffer TreatmentNeutralization Buffer Incubation