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Related Concept Videos

Flow Cytometry01:23

Flow Cytometry

The development of flow cytometry techniques began in 1934 with initial attempts by Andrew Moldavan, a bacteriologist who counted the cells in a flowing capillary system. Moldavan pumped cells through a capillary tube focused under a microscope for visualization. The invention of photometry allowed the measurement of differentially-stained cells, and Louis Kamentsky developed the first multiparameter flow cytometer in 1965 to identify and count the cancer cells in cervical tissue specimens.
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Related Experiment Video

Updated: May 9, 2026

An Automated Method to Perform The In Vitro Micronucleus Assay using Multispectral Imaging Flow Cytometry
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Flow cytometric determination of micronucleus frequency.

Azeddine Elhajouji1, Magdalena Lukamowicz-Rajska

  • 1Genetic Toxicology and Safety Pharmacology, Preclinical Safety, Novartis Institutes for Biomedical Research, Basel, Switzerland.

Methods in Molecular Biology (Clifton, N.J.)
|July 31, 2013
PubMed
Summary

The micronucleus (MN) test is a valuable biomarker for chromosomal damage, widely used in genotoxicity screening. Its versatility and automation potential, especially with flow cytometry, solidify its role in toxicological research and regulatory settings.

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Area of Science:

  • Toxicology
  • Genetics
  • Cell Biology

Background:

  • The micronucleus (MN) test is a widely adopted method for assessing genotoxicity.
  • Micronuclei serve as biomarkers for chromosomal damage and mitotic abnormalities.
  • The assay's versatility stems from its simplicity, accuracy, and adaptability to various cell types and experimental settings.

Purpose of the Study:

  • To provide an overview of the micronucleus test protocol designs and experimental steps.
  • To detail the accurate analysis of micronuclei using flow cytometry.
  • To highlight the MN test's significance in genotoxicity screening and toxicological investigations.

Main Methods:

  • Utilizing the micronucleus (MN) test as a genotoxicity screening tool.
  • Applying image analysis or flow cytometry for automated scoring.
  • Implementing established OECD guidelines for both in vitro (487) and in vivo (474) MN tests.

Main Results:

  • The MN test has been extensively used for over two decades in genotoxicity screening.
  • The assay's ease of use, accuracy, and automation have significantly advanced understanding of genotoxins.
  • Recent guideline acceptances (OECD 487 and 474) reinforce the MN test's critical role in research and regulatory toxicology.

Conclusions:

  • The micronucleus test is a versatile and crucial tool for evaluating genotoxicity.
  • Flow cytometry offers an accurate and efficient method for MN analysis.
  • The MN test is indispensable for both exploratory research and regulatory genotoxicity assessment.