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Apcmin

Manufactured by Jackson ImmunoResearch
Sourced in France

ApcMin/+ is a laboratory mouse model that carries a mutation in the Apc (adenomatous polyposis coli) gene. This mutation leads to the spontaneous development of multiple intestinal adenomas, which are a type of benign tumor.

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23 protocols using apcmin

1

Circadian Knockout Impacts Intestinal Tumorigenesis

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Mice were housed on a 12-hour light/12-hour dark cycle with ad libitum food in a barrier facility. Apcmin mice (#002020; Jackson Labs, Bar Harbor, ME) were crossed with Bmal1+/- null mutant mice (#009100; Jackson Labs). Progeny were back-crossed for 7 generations to generate a genetically pure strain before experiments began. Bmal1flox/flox mice (#007668; Jackson Labs) were crossed with VillinCre/+ mice (#021504; Jackson Labs), or Apcmin mice, then the 2 strains were crossed to obtain the Apcmin/+; Bmal1flox/flox and Apcmin/+; VilCre/+; Bmal1flox/flox for the cKO experiments. Genotyping was performed according to protocols available at Jackson Labs (www.jax.org). All animals were tested for tumor initiation at 1 or 3 months of age. Mice maintained under constant light (LL) were housed in these conditions from 21 days of age to 3 months of age. Light levels were approximately 700 Lux, measured at the back of each cage, and all objects were removed so that light fully penetrated throughout each cage. Mice were maintained under Canadian Council for Animal Care guidelines (University of Windsor: AUPP 17-21).
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2

Genetic Manipulation of Mouse Models

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Housing of mice and in vivo experiments were performed in compliance with the European Communities Council Directive of 24 November 1986 (86/609/EEC) and national and institutional guidelines. Animal care and experimental procedures were approved by the Animal Care Committee of the Institute of Molecular Genetics (no. 71/2014). ApccKO/cKO mice were obtained from the Mouse Repository (National Cancer Institute, Frederick, MD, US); Villin-CreERT2 and Villin-Cre mice14 (link) were kindly provided by S. Robine (Institut Curie, Centre de Recherche, Paris, France); Apc+/Min, Lgr5-EGFP-IRES-CreERT2, Msx1cKO/cKO, and immonodeficient NSG™ mice were purchased from the Jackson Laboratory (Bar Harbor, ME, US). Animals were housed in specific pathogen-free conditions.
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3

Genetic Mouse Models for Colorectal Cancer

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WT C57BL/6J (Cat # 000664), APCmin/+ (Cat # 002020), Lgr5-EGFP-IRES-creERT2 (Cat # 008875) and APCflox mice (Cat # 009045) were purchased from Jackson Laboratory. FXRflox mice were kindly provided by Dr. Pierre Chambon (University of Strasbourg, France) and maintained in the Evan’s laboratory. All animal experiments were performed in the specific pathogen-free facilities at the Salk Institute following the Institutional Animal Care and Use Committee’s guidelines.
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4

Breeding and Maintenance of C57BL/6J and ApcMin/+ Mice

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C57BL/6J and ApcMin/+ mice were originally purchased from Jackson Laboratory and bred inhouse for the experiments. Mice were maintained in IVC cages and kept in a 12-h/12-h dark-light cycle at 20–22 °C and 40–60% humidity with free access to food and water. All the mice were fed with PicoLab®Rodent Diet 20-5053 (LabDiet, USA).
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5

Inducible Genetic Manipulation in Mice

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Housing of mice and in vivo experiments were performed in compliance with the European Communities Council Directive of 24, November 1986 (86/609/EEC) and national and institutional guidelines. Animal care and experimental procedures were approved by the Animal Care Committee of the Institute of Molecular Genetics (ref. 58/2017). ApccKO/cKO mice [41 (link)] were obtained from the Mouse Repository (National Cancer Institute, Frederick, MD, USA); Villin-CreERT2 mice [42 (link)] were kindly provided by Sylvie Robine (Institut Curie, Centre de Recherche, Paris, France); Apc+/Min (C57BL/6J-ApcMin/J) [43 (link)], Ki67-RFP (Mki67tm1.1Cle/J) [44 (link)], Lgr5-EGFP-IRES-CreERT2 (B6.129P2-Lgr5tm1(cre/ERT2)Cle/J) [45 (link)], and Rosa26-tdTomato (B6;129S6-Gt(ROSA)26Sortm14(CAG-tdTomato)Hze/J) [46 (link)] mice were purchased from the Jackson Laboratory (Bar Harbor, ME, USA). The animals were kept under specific pathogen-free conditions. To induce Cre-mediated gene recombination, mice were gavaged with 1 mg tamoxifen (Merck). tamoxifen was dissolved in ethanol (100 mg/mL) and combined (1:9) with mineral oil (Merck) before administration. Mice were sacrificed by cervical dislocation at various time points after administration of a single dose (100 µL) of the tamoxifen/oil solution.
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6

Genetic Mouse Models for Intestinal Research

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Animal experiments were approved by the National Animal Experiment Board of Finland. Mice were housed and monitored according to the Federation of European Laboratory Animal Science Associations guidelines and recommendations. The mice were weighed and their health was closely monitored during the experiment. The mouse lines Lef1fl/fl (25 (link)), Apcfl/fl (76 (link)), Lgr5-EGFP-IRES-CreERT2 (4 (link)), Rosa26LSL-TdTomato (Jackson Laboratory, stock no. 021875), ApcMin/+ (Jackson Laboratory, stock no. 002020), Villin-CreERT2 (Jackson Laboratory, stock no. 020282), and Villin-Cre (Jackson Laboratory, stock no. 021504) have been described previously. Lef1fl/fl mice with mixed C57BL/6 and 129SV background were used after backcrossing to the C57BL/6 strain for >6 generations. All experiments were performed three times with independent cohorts. Approximately equal numbers of male and female mice of same age were used for all the experiments.
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7

Comparative Study of C57BL/6J and ApcMin/+ Mice

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C57BL/6J and ApcMin/+ mice were purchased from The Jackson Laboratory. Stat6−/− mice on C57BL/6J background were kindly provided by Dr. Joe Craft (Yale University). Both male and female mice at 15 weeks were used in all experiments. WT littermates were used as controls. All mouse protocols were approved by the Yale University Institutional Animal Care and Use Committee.
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8

Murine Models for Cancer Research

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Wild-type C57BL/6J mice (Stock no. 000664), Vav-icre mice (Stock no. 008610), R26-CreErt2 mice (Stock no. 008463), Il22ra1-floxed (Stock no. 031003), CD45.1 C57BL/6J mice (Stock no. 002014), Trp53−/− (Stock no. 002101), Cd4-cre (Stock no. 022071), and ApcMin (Stock no. 002020) mice were purchased from The Jackson Laboratory. Il22−/− mice were provided by R. Caspi (National Institutes of Health, Bethesda, MD) with permission from Genentech (San Francisco, CA). Epor-cre53 mice were a gift from U. Klingmüller (Deutsches Krebsforschungszentrum (DFKZ), Germany). Il22-tdtomato (Catch-22)54 mice were a gift from R. Locksley (University of California at San Francisco, CA). Rps14-floxed mice55 were a gift from B. Ebert (Dana-Farber Cancer Institute, Boston, MA). Mice were housed in the Animal Research Facility (ARF) at DFCI under ambient temperature and humidity with 12 h light/12 h dark cycle. Animal procedures and treatments were in compliance with the guidelines set forth by the Institutional Animal Care and Use Committee (IACUC) at DFCI. Age- and gender- matched mice were used within experiments.
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9

Genetically Modified Mouse Models

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C57BL/6J, Rag1−/−, CCR6−/−, OT-II and APCMin/+ mice on C57BL/6 background were obtained from Jackson Laboratories. Myd88−/− mice on C57BL/6 background were kindly provided by S. Akira (Osaka Univ., Osaka, Japan), and were crossed to APCMin/+ mice. All animal procedures were approved by the University of Louisville Institutional Animal Care and Use Committee.
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10

Genetic Regulation of Intestinal Homeostasis

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C57BL/6J (WT) and APCmin/+ mice were purchased from The Jackson Laboratory. Nlrp12–/– mice were generated by Millennium Pharmaceuticals. Nlrp12fl/fl mice were generated by our laboratory with the help of the UT Southwestern Mouse Transgenic Core facility. The background of all mice used in this study is C57BL/6J. Unless otherwise stated, mice of different genetic backgrounds were housed in separate cages, maintained in the same animal room, and used for in vivo and in vitro experiments. All mice were bred and maintained in a specific pathogen–free (SPF) facility at the UT Southwestern Medical Center. For cohousing experiments, 4-week-old WT mice were cohoused with Nlrp12–/– mice for 30 days. All animal studies were conducted with age- and sex-matched mice.
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