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Trp53fl fl mice

Manufactured by Jackson ImmunoResearch

Trp53fl/fl mice are genetically engineered mice that have the p53 gene (Trp53) flanked by loxP sites, allowing for conditional deletion of the gene. The p53 gene is a tumor suppressor gene that plays a crucial role in regulating cell growth and division. These mice can be used to study the functional impact of p53 in various biological processes and disease models.

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3 protocols using trp53fl fl mice

1

Genetically Modified Mouse Models

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Gen1−/− mice were generated at the Memorial Sloan Kettering Cancer Center Mouse Genetics Core Facility. Mus81fl/fl mice were generated using ES cell clone purchased from EUCOMM (Skarnes et al., 2011 (link)). Mb1 (Cd79a)-Cre mice were purchased from The Jackson Laboratory (strain #:020505) (Hobeika et al., 2006 (link)). Cd23-Cre (Kwon et al., 2008 (link)) and Aicda−/− (Muramatsu et al., 2000 (link)) mice were gifted by Meinrad Busslinger (Research Institute of Molecular Pathology, Austria) and Tasuku Honjo (University of Kyoto, Japan), respectively. Trp53fl/fl mice were purchased from The Jackson Laboratory (strain #:008462) (Marino et al., 2000 (link)). Experiments were performed using mice between 8- and 16-week-old. When littermate controls were unavailable, age-matched controls were employed in experiments. All mice were housed and maintained in groups of five under specific pathogen-free conditions, and euthanized at the time of analyses in accordance with guidelines for animal care established by Memorial Sloan Kettering Cancer Center Research Animal Resource Center and the Institutional Animal Care and Use Committee (IACUC).
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2

Transgenic Mouse Models for Tumor Studies

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C57BL/6, Ms4a3-tdTom reporter and CD169-DTR (ref. 33 (link)) male and female mice of 8–12 weeks old were used for tumour experiments (each experiment was sex-controlled). Mice were maintained at specific-pathogen free (SPF) health status in individually ventilated cages at 21–22 °C and 39–50% humidity, under 12-h light–dark cycles. KP mice15 (link) were generated by crossing LSL-K-rasG12D mice (Jackson Laboratories, Jax ID: 008179) with Trp53fl/fl mice (purchased from Jackson Laboratories, Jax ID: 008462). CD169cre/+ mice34 (link) were donated by P. Frenette and backcrossed to R26-LSL-tdTomato (Jackson Laboratories, Jax ID: 007914). Ethical approval for mouse experiments was obtained by the Internal Animal Care and Use Committee at Mount Sinai Hospital.
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Genetic Mouse Models for Cancer Research

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Rosa26-YFP mice42 (link), Lgr5-creER mice43 (link), KrasLSLG12D mice44 (link) and Trp53fl/fl mice45 (link) were imported from the NCI mouse repository and Jackson Laboratories. NOD/SCID/Il2Rγ null mice were purchased from Charles River. All mouse groups used in this study were composed of males and females with mixed genetic background. No randomization and no blinding were performed in this study. The Rosa26LSL-NTN1 transgenic mice (for LKPR-NTN1 gain of function) were imported from Mehlen Laboratory-Apoptosis, Cancer and Development, Centre de Recherche en Cancérologie, Lyon, France46 (link).
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