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Related Concept Videos

Mutation, Gene Flow, and Genetic Drift01:09

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In a population that is not at Hardy-Weinberg equilibrium, the frequency of alleles changes over time. Therefore, any deviations from the five conditions of Hardy-Weinberg equilibrium can alter the genetic variation of a given population. Conditions that change the genetic variability of a population include mutations, natural selection, non-random mating, gene flow, and genetic drift (small population size).
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Related Experiment Video

Updated: Jan 20, 2026

Annexin V Binding Assay: A Fluorescence-Based Technique to Identify Apoptotic Erythrocytes via Phosphatidylserine Labeling
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Erythrocyte-Based Pig-a Gene Mutation Assay.

Jeffrey C Bemis1, Nikki E Hall1, Stephen D Dertinger2

  • 1Litron Laboratories, Rochester, NY, USA.

Methods in Molecular Biology (Clifton, N.J.)
|September 2, 2019
PubMed
Summary
This summary is machine-generated.

The Pig-a gene mutation assay detects genotoxicity by identifying red blood cells with a specific cell surface defect. This flow cytometry method is crucial for preclinical safety testing.

Keywords:
Endogenous mutationErythrocytesFlow cytometryGenotoxicityGlycosylphosphatidylinositol (GPI) anchorHigh throughputImmunomagnetic separationPig-aReticulocytes

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Area of Science:

  • Toxicology
  • Genetics
  • Biomedical Science

Background:

  • Genotoxicity testing is vital in preclinical safety evaluations.
  • Assessing gene mutations complements chromosomal damage analysis.
  • The Pig-a gene assay offers a sensitive method for detecting mutations.

Purpose of the Study:

  • To describe a standardized procedure for the Pig-a gene mutation assay.
  • To detail the use of MutaFlow® kits for sample processing.
  • To outline flow cytometric analysis of red blood cells for genotoxicity.

Main Methods:

  • Utilizes the Pig-a gene mutation assay based on loss of gene function.
  • Assesses the lack of cell surface protein expression due to GPI anchor defects.
  • Employs flow cytometry for analyzing red blood cell phenotypes.

Main Results:

  • The described procedure enables reliable detection of Pig-a gene mutations.
  • Flow cytometry effectively identifies cells with the specific cell surface phenotype.
  • MutaFlow® kits facilitate consistent sample processing.

Conclusions:

  • The Pig-a gene mutation assay is a valuable tool in genotoxicity testing.
  • Standardized procedures enhance the reliability of preclinical safety assessments.
  • Flow cytometry provides an efficient method for evaluating red blood cell mutations.