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C57bl 6j b6 h 2b

Manufactured by Charles River Laboratories
Sourced in China

The C57BL/6J (B6; H-2b) is a widely used inbred mouse strain. It is a commonly used laboratory mouse model with a well-characterized genetic background.

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3 protocols using c57bl 6j b6 h 2b

1

Heterotopic Heart Transplantation in Mice

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Eight to ten-week-old male C57BL/6J (B6; H-2b) and BALB/c (H-2d) mice were purchased from Charles River (Beijing, China). All mouse experiments were performed in a specific pathogen-free facility according to the guidelines of the animal care and use committee of Huazhong University of Science and Technology and complied with the National Institutes of Health (NIH) Guidelines for the care and use of laboratory animals. We established a murine heterotopic heart transplantation model as previously described 10 (link), animals were anesthetized using 2% isoflurane and administered via nose cone mask. All animals were euthanized using CO2 asphyxiation, followed by cervical dislocation to obtain tissue samples. In the allograft group, BALB/c hearts were transplanted into fully MHC-mismatched B6 recipients. In the control group, B6 hearts were transplanted into MHC-matched B6 recipients.
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2

Mouse Experiments for Immunology Research

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Mouse experiments were approved by the University of Cambridge Ethical Review Panel and carried out in accordance with Home Office Project Licence PPL 80-2347. C57BL/6J (B6; H-2b) and BALB/c (H-2d) mice were purchased from Charles River UK. D8 mice (H-2Dd expressing C57BL/6J transgenic mice) have been described16 (link). Expression of the additional MHC gene in these mice is comparable to endogenous H-2Dd expression in BALB/c mice. Rag2−/−and Rag2−/−Il2rg−/−mice (both H-2b) have been described28 (link)29 (link). B6.Rag2−/−mice lack functional B and T lymphocytes, and the remaining immature pro-B and pro-T cells cannot rearrange their antigen receptors and thus fail to achieve antigen specificity. Rag2−/−Il2rg−/−mice also lack NK cells due to defective IL-15 signalling. B6 or D8 males were randomly introduced to virgin mice at 7–10 weeks of age, and the timing of conception was determined by detection of a copulation plug representing gd0.5.
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3

Generation and Characterization of Macrophage-specific Map2k1/Map2k2 Knockout Mice

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Male C57BL/6J (B6; H-2b) and BALB/c (H-2d) mice (aged 8–10 wk) were purchased from the Charles River (Beijing, China). Lyz2Cre mice (C57BL/6 background) and B6.C-H-2bm12 (Bm12) mice were purchased from Jackson Laboratory (USA). Map2k1 and Map2k2 flox mice were generated using Shanghai Model Organisms (Shanghai, China) on a C57BL/6 background. Specifically, the Map2k1 flox mice were obtained by transcription activator-like effector nucleases–mediated insertion of loxP sites in the Map2k1 gene, whereas the Map2k2 flox mice were obtained by CRISPR/Cas9-mediated insertion of loxP sites in the Map2k2 gene. Macrophage-specific Map2k1 and Map2k2 double-gene knockout (DKO) mice were generated by crossing Map2k1 and Map2k2 flox mice with Lyz2Cre mice. The genotype primer sequences of these mice are listed in Table S3 (SDC, http://links.lww.com/TP/C952). Animal protocols were reviewed and approved by the Institutional Animal Care and Use Committee of Huazhong University of Science and Technology. All mouse experiments were performed in a special pathogen-free facility according to the Animal Care and Use Committee of Huazhong University of Science and Technology guidelines and in accordance with the National Institutes of Health Guidelines for the Care and Use of Laboratory Animals. CO2 asphyxiation was performed for euthanasia.
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