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Nod caj mice

Manufactured by Jackson ImmunoResearch

NOD/Caj mice are a strain of laboratory mice developed for research purposes. They are commonly used as a model for type 1 diabetes. These mice have a genetic predisposition to develop autoimmune diabetes, which can be useful for studying the underlying mechanisms of the disease.

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3 protocols using nod caj mice

1

Diabetes Development in NOD Mouse Models

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NOD/LtJ mice purchased from the Jackson Laboratory were used for studying diabetes development. NOD/Caj mice were originally obtained from the Jackson Laboratory (NOD/LtJ) and have been maintained at Yale University for over 25 years. MyD88−/−NOD mice were generated as described previously [20 (link)] and have been maintained at Yale University for over 7 years. MyD88−/−B6 mice were kindly provided by Dr. Akira [21 (link)] and have been maintained at Yale University for over 10 years. B6g7 breeders were kindly provided by Drs. Mathis and Benoist (Harvard University) and have been bred at Yale University for over 10 years. MyD88−/−B6g7 mice were generated by breeding B6g7 with MyD88−/−B6 mice. C57BL/6J (B6) mice were originally obtained form the Jackson Laboratory and have been maintained at Yale University for over 5 years. All mice used in this study were kept in the same room, in specific pathogen–free conditions, in a 12-hour dark/light cycle and housed in individually-ventilated filter cages with autoclaved food at the Yale University animal facility. The use of the animals in this study was approved by the Yale University Institutional Animal Care and Use Committee.
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2

NOD Mouse Model for Autoimmune Diabetes

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All the mice used in this study were kept in specific pathogen-free conditions with a 12-h dark/light cycle at the Yale University animal facility. NOD/Caj mice were originally obtained from the Jackson Laboratory and have been maintained at Yale University. Tlr7−/− C57BL/6 breeders, which were kindly provided by Prof. Richard Flavell (Yale University),22 (link) were backcrossed to the NOD/Caj genetic background for 12 generations. The purity of the NOD genetic background was examined by mouse genome scan using an Illumina SNP chip (DartMouse). BDC 2.5 CD4+ TCR transgenic NOD mice, NY8.3 CD8+ TCR transgenic mice and Rag-deficient (Rag−/−) NOD mice were originally obtained from the Jackson Laboratory and have been maintained at Yale University. The use of the animals in this study was approved by the Institutional Animal Care and Use Committee of Yale University.
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3

Transgenic NOD Mouse Models for T1D

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NOD/Caj mice were originally obtained from the Jackson Laboratory and have been maintained at Yale University for over 30 yrs. 2H6TCRαβ NOD mice (designated 2H6; expressing the TCRα chain Vα6/Jα45/Cα and the TCRβ chain Vβ14/Dβ1.1/Jβ2.3/Cβ2) were generated, as previously described (8 (link), 19 (link)), and maintained at Yale University. VH125 NOD mice, expressing the heavy chain of the insulin-reactive monoclonal antibody (mAb) 125 were generated by Dr James Thomas (Vanderbilt University) (12 (link)) and obtained from the Jackson Laboratory (Bar Harbor, Maine). Approximately >95% of these VH125 B cells were IgMa, indicating a high level of allelic exclusion (data not shown). 2H6VH125 NOD mice were obtained by breeding 2H6 NOD mice with VH125 NOD mice. Recombinase-activating-gene deficient NOD (Rag-/-NOD) mice were originally obtained from the Jackson Laboratory and maintained at Yale University. All the mice used in this study were kept in specific pathogen–free (SPF) conditions, in a 12-hour dark/light cycle and housed in individually-ventilated filter cages with free access to water and autoclaved food at the animal facility of Yale University. The Yale University Institutional Animal Care and Use Committee approved the usage of animals and the procedures used in this study.
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