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C57bl 6j male

Manufactured by Janvier Labs
Sourced in France

The C57BL/6J male is a widely used inbred mouse strain. It is a laboratory animal model that serves as a standard reference strain for genetic and biomedical research.

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5 protocols using c57bl 6j male

1

Aging Study on C57BL/6J Mice

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Animal experiments were performed in accordance with the Swiss ordinance on animal experimentation, after approval by Kantonales Veterinäramt Basel-Stadt (Schlachthofstrasse 55, 4056 Basel). Adult C57BL/6J male mice aged 12 and 24 months were purchased from Janvier Laboratories (France) and subsequently maintained in Novartis animal care facilities at 22 °C in a 12-h light–12-h dark cycle with unrestricted access to regular diet and water.
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2

Generation and Characterization of Multiple Knockout Mice

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The generation and characterization of the double (TNF receptor-associated factor 2 (Traf2) and Caspase-8 (Casp8)) and the triple (Traf2, Casp8, and Receptor-interacting serine/threonine-protein kinase 3(Ripk3); and the Traf2, Casp8, and Inhibitor of nuclear factor kappa-B kinase subunit beta (Ikbkb)) KO mice included in this study were published by our group in [27 (link)]. The hydrodynamic tail vein injections (HDTVi) were performed as described in [28 (link)]. In brief, 5-week-old wild-type C57BL/6J male mice were ordered from Janvier Labs (Le Genest, Pays de la Loire, France), and allowed recovery for two weeks before HDTVi. For HDTVi, 7-week-old mice were anesthetized with Isoflurane (Piramal, Andhra Pradesh, India) and vectors (i.e., 25 µg transposon vector (carrying c-Myc and NRAS oncogenes) and 5 µg SB13 transposase vector) were delivered in 10% v/w body weight of physiological solution (0.9% NaCl) in the mouse’s tail vein. Animals were euthanized 6 weeks after the procedure. For fibrosis induction, wild-type mice (C57BL/6J) were injected twice a week in the peritoneum with 50 µL of CCl4 (6 µL CCl4/10 g body weight/Oil up to 50 µL), while control animals were injected with 50 µL of oil.
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3

Zebrafish and Mice Experiments Protocols

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This study was conducted in accordance with the French and European Community guidelines for the use of animals in research (86/609/EEC and 2010/63/EU) and approved by the local Ethics Committee from the CYROI platform for animal experimentation (APAFIS#2018040507397248_v3; APAFIS# 20200908140689_v5).
For zebrafish (Danio rerio), adult (3–6 months-old) male and female wild-type (WT), tg(fli1:EGFP)54 (link), and tg(GFAP::GFP)55 (link) were maintained under standard conditions on a 14/10-h (h) light–dark cycle at 28.5 °C, and were fed daily with commercially available dry food (Gemma 300, Skretting). Fish were from the AB strain: WT, tg(GFAP::GFP), and tg(fli1:EGFP).
For mice (Mus musculus), C57BL/6J male (8 week-old, 25 g) mice were purchased from JANVIER LABS (Le Genest-Saint-Isle, France). They were maintained under standard conditions of light, temperature, and humidity and fed a standard diet ad libitum.
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4

Conditional Deletion of PRKAA1 in Endothelial Cells

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All animals were housed with a 12-h/12-h light/dark cycle, with the dark cycle occurring from 6.00 p.m. to 6.00 a.m. Mice were observed daily with free access to water and standard chow. C57BL/6J males (age 8-12wk) were purchased from the Janvier labs (Le Genest Saint Isle, France). C57BL/6J Cdh5-iCreERT2 mice56 (link) were kindly provided by Ralf Adams, and crossed with mice carrying a floxed allele of PRKAA1 gene (PRKAA1fl/fl, #014141, the Jackson Laboratory). Cdh5-iCreERT2+ /− PRKAA1fl/fl mice were administered Tamoxifen (500 μg, intraperitoneally) for five consecutive days at 8 weeks, and used for experiment three weeks after the last Tamoxifen injection. The animals were maintained under a 12:12-h light–dark cycle with free access to food and water.
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5

CRISPR-Cas9 Mediated Generation of Brme1 Mutant Mice

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Mouse zygotes were collected from superovulated 3–4-week-old C57BL/6J females (Janvier Labs) mated with C57BL/6J males (Janvier Labs) overnight. SpCas9 protein (30 ng/µl; Sigma) and sgRNA (12.5 ng/µl) were mixed to form ribonucleoprotein complexes and injected into zygotes in M2 medium. Injected zygotes were allowed to recover for 2–4 h in KSOM medium in a humidified CO2 incubator at 37°C and then were transferred into pseudopregnant 8–20-week-old SWISS female mice (Janvier Labs). For identification of founders, ear punch biopsies were subjected to DNA-extraction procedures, and the extracted DNA was amplified with primers flanking the sgRNA target site. PCR products from each founder were sequenced, and the mutated founder mice were crossed with C57BL/6J WT mice to avoid potential off-target mutations. The Brme1 allele was genotyped using the following primers: Forward; 5′-TTCAGGGTAGGATAGGATGGGG-3′, Reverse; 5′-CTTGTAATCTGCTGCAGCCT-3′.
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