Advantages of Congenic Strains
Genetically defined rodent strains with stable, identifiable phenotypes are essential to biomedical research. However, complex gene interactions can result in genetic variability in rodent strains, possibly affecting the observed phenotype. Congenic strains minimize genetic variability in experiments and reveal insights into the contribution of background strains on model phenotypes. Developed through selection and backcrossing, these strains require periodic genetic monitoring to maintain purity before research or breeding.
Background strain characterization detects genetic variation which can arise in closed colonies or through misbreeding. Research models are often exchanged among many institutions, making their precise breeding history difficult to track. No matter how well managed colonies are, routine background confirmation is essential. Protect your research and budget by conducting studies with genetically verified models that meet your testing requirements.
Does Your Research Require the Transfer of Genetic Backgrounds?
We can deliver your desired genome through our congenicity testing and identifying individuals containing more of the recipient genome from each generation. Whereas with traditional/random backcrossing methods, it takes 10 generations (~2.5 years) to produce a congenic strain.
Application Highlights for Speed Congenics/MAX-BAX Program | |
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| Single-Round • Verify inbred and outbred backgrounds • Detect genetic contamination • Assess genetic diversity in outbred models • Cell line characterization • Linkage analysis • Mutation mapping • Map transgene insertion • Recombination event detection | Multiple-Round • Desired genotype in fewer than five generations • Custom-designed mouse 384 SNP panel for all donor and recipient strains • Genome-wide microsatellite panels (mice & rats) • All autosomes and X chromosome covered in all panels • Y-chromosome markers tested if necessary • Learn more about our housing and breeding services |
Which SNP-Panel is Appropriate for Your Research?
Mouse 384 SNP Panel (MAX-BAX®) Complete Background Analysis
Mouse B6 128 SNP Panel for Congenic C57BL/6 Mice
Rat 240 SNP Panel Complete Background Analysis
Mouse or Rat 32 SNP QC Panel for Line Contamination
Frequently Asked Questions About Our Genetic Research Services
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How should I prepare to test using the 128 SNP B6 strain panel?
Before using the B6 128 SNP panel, we need to ensure that your mice are congenic for C57BL/6 and have been backcrossed for at least three known generations. Otherwise, they must be run through one round of 384 SNP to make sure they truly are C57.
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How many samples do I need to run for each MAX-BAX panel?
If you are looking to make your line congenic, we recommend n=10 samples per-generation per-line.
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How many samples do I submit for background strain characterization?
To do a background strain characterization you can randomly choose between two and ten samples to ensure a broad picture of the line has been gathered.
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How will I move forward with my results 128 SNP B6 strain panel (or any other strains)?
The mice in the line that show up with a higher congenital percentage will be chosen to continue to breed the colony for further generations.
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Are mouse 384 SNP analysis tests known by any other name?
Yes. Mouse 384 SNP analysis tests are also known as MAX-BAX, Speed Congenics, and Accelerated Backcrossing.
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How often should I do a mouse or rat 32-marker assay for contamination detection?
The quality of your lines genetic background is important for research consistency. If you are doing closed colony breeding, we recommend running a mouse and rat 32-marker assay, we suggest you test annually at minimum.
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What is the definition of congenic?
The Charles River definition of congenic means we are testing to get your line to ~99.95% desired in-bred background strain.
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When do you recommend background strain characterization?
We recommend background strain characterization in the following situations:
- When establishing a closed breeding colony
- When new strains are received from collaborators
- During backcrossing (to check extent and/or for speed congenics)
- If unusual phenotypes appear
- At the commencement of a series of experiments
- Annual monitoring of in-house colonies
Generation Traditional Backcross
Recipient GenomeSpeed Congenics/MAX-BAX
Recipient GenomeF1 50.00% ~50.00% N2 75.00% ~80.00% N3 87.50% ~94.00% N4 93.75% ~99.00% N5 96.88% ~100.00% N6 98.44% N7 99.22% N8 99.61% N9 99.81% N10 99.90%