C57BL/6J mice are resistant to audiogenic seizures, have a relatively low bone density, and develop age related hearing loss. They are also susceptible to diet-induced obesity, type 2 diabetes, and atherosclerosis.

Apr 3, 2013 · If you need to know whether your mouse has a C57BL/6J (B6J, 000664), C57BL/6N (B6N, 005304), or mixed B6J;B6N background, The Jackson Laboratory’s (JAX’s) new C57BL/6 Substrain Characterization Panel may be just the tool you need.

For over a century, the Jackson Laboratory has raised and distributed countless C57BL/6J mice. But has anyone wondered why this particular mouse, first bred in 1921 by Jackson Laboratory founder C.C. Little, has been so popular or acquired its name?

Aged C57BL/6J mice have research applications that include immunology, cancer, longevity interventions, and biomarker studies. C57BL/6J is the most widely used inbred mouse strain and the first to have its genome sequenced.

C57BL is probably the most widely used of all inbred strains, (substrain C57BL/6 alone accounts for over 14% of occasions on which an inbred strain is used) though in many ways it seems to be atypical of inbred strains of laboratory mice.

Jun 22, 2016 · A mutation that causes spotty retinal degeneration, known asCrb1rd8was discovered to be homozygous in all C57BL/6N related substrains, but is not present in the C57BL/6J substrain. Additionally, data collected from the International Knockout Mouse Consortium ( IKMC ) phenotyping centers has found numerous phenotypic differences between the ...

Dec 10, 2024 · View mouse strain C57BL/6J : mutations, QTL, phenotypes, diseases, and references.

005304 C57BL/6NJ This is an NIH subline of C57BL/6. It was separated from C57BL/6J in 1951. Five SNP differences have been identified that distinguish C57BL/6J from C57BL/6ByJ and C57BL/6NJ.

View mouse strain C57BL/6NTac : mutations, QTL, phenotypes, diseases, and references.

C57BL/10J mice are a valuable immunological research tool. They have a high lymphocyte phytohaemagglutinin response, a good immune response to ovalbumin, a poor response to DNP-keyhole limpet haemocyanin and are resistant to induction of passive cutaneous anaphylaxis (IgG1- and IgE- mediated).