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Related Concept Videos

Mouse Models of Cancer Study02:43

Mouse Models of Cancer Study

Mice have long served as models for studying human biology and pathology because of their phylogenetic and physiological similarity with humans. They are also easy to maintain and breed in the laboratory, and hence, many inbred strains are now available for research. Studies on mice have contributed immeasurably to our understanding of cancer biology.
The development of transgenic, knockout, and knock-in mice has led to an exponential increase in their use as model organisms in research,...
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In-vitro Mutagenesis

To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.

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Related Experiment Video

Updated: Jun 12, 2026

Murine Distal Colostomy, A Novel Model of Diversion Colitis in C57BL/6 Mice
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Published on: July 12, 2018

Genetic polymorphisms among C57BL/6 mouse inbred strains.

Esther Zurita1, Mónica Chagoyen, Marta Cantero

  • 1Department of Molecular and Cellular Biology, Centro Nacional de Biotecnología (CNB-CSIC), Campus de Cantoblanco, Darwin 3, 28049, Madrid, Spain.

Transgenic Research
|May 28, 2010
PubMed
Summary

Genetic differences exist among C57BL/6 mouse substrains, impacting their use in research. Identifying these genetic variations is crucial for accurate animal model development and colony management.

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Area of Science:

  • Genetics
  • Animal Models
  • Biotechnology

Background:

  • C57BL/6 mice are widely used for transgenic and knockout models.
  • Existing C57BL/6 substrains exhibit genetic and phenotypic variations.
  • Long-term separation of breeding stocks can lead to accumulated genetic differences.

Purpose of the Study:

  • To characterize the genetic differences among various C57BL/6 substrains.
  • To identify informative genetic markers for distinguishing C57BL/6 substrains.

Main Methods:

  • Utilized the Illumina Mouse Medium Density Linkage Mapping panel.
  • Analyzed 1,449 single nucleotide polymorphisms (SNPs) across ten C57BL/6-related strains.
  • Identified twelve informative SNPs for substrain discrimination.

Main Results:

  • C57BL/6J substrains from different sources were genetically indistinguishable.
  • All C57BL/6N substrains showed identical genotypes.
  • Other C57BL/6 substrains displayed intermediate genetic profiles with unique polymorphisms.

Conclusions:

  • Genetic monitoring of C57BL/6 substrains is essential.
  • Understanding substrain-specific genetic variations is critical for accurate mouse colony handling.
  • These findings support the appropriate use of distinct C57BL/6 substrains in research.