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Lox stop lox rosa diphtheria toxin mice

Manufactured by Jackson ImmunoResearch
Sourced in United States

The Lox‐stop‐lox‐Rosa diphtheria toxin mice are a lab animal model that expresses the diphtheria toxin in a conditional manner. The expression of the toxin is controlled by the Lox‐stop‐lox system, allowing for targeted and regulated cell death in specific cell populations.

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2 protocols using lox stop lox rosa diphtheria toxin mice

1

Adipose-Deficient Mice Physiology

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Experiments were performed on male fat‐free (FF) and wild‐type (WT) littermate control mice on a C57BL/6J background. FF mice were generated by crossing adiponectin‐Cre mice (The Jackson Laboratory, Bar Harbor, ME, USA: 028020) with lox‐stop‐lox‐Rosa diphtheria toxin mice (The Jackson Laboratory: 010527) (Collins et al., 2020 ; Wu et al., 2018 ). The resulting FF mice constitutively have a complete absence of adipose tissue from birth. These mice and DTA/+ littermate WT control were maintained at thermoneutrality (30°C) on a chow diet (10% fat) with free cage activity. Exact animal numbers used in each experiments are listed in the figure legends. Complement factor D constitutive knockout mice were used to determine the role of adipsin in the FF muscle physiology phenotype (a generous gift from Drs Atkinson and Wu; Wu et al., 2018 ).
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2

Adipose-Deficient Mouse Model for Muscle Physiology

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Experiments were performed on male fat-free (FF) and wildtype (WT) littermate control mice on a C57BL/6J background. FF mice were generated by crossing adiponectin-Cre mice (Jackson Labs: 028020) with lox-stop-lox-Rosa diphtheria toxin mice (Jackson labs: 010527) (Wu et al., 2018 (link); Collins et al., 2020 ). The resulting FF mice constitutively have a complete absence of adipose tissue from birth. These mice and DTA/+ littermate WT control were maintained at thermoneutrality (30°C) on a chow diet (10% fat) with free cage activity. Exact animal numbers used in each experiment is listed in the figure legend. Complement factor D constitutive knockout mice were used to determine the role of adipsin in the FF muscle physiology phenotype (generous gift from Drs. Atkinson and Wu (Wu et al., 2018 (link))).
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