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B6 cg cav1tm1mls j

Manufactured by Jackson ImmunoResearch
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B6.Cg-Cav1tm1Mls/J is a genetically engineered mouse strain. It contains a targeted mutation in the Cav1 gene, which encodes the caveolin-1 protein. This strain is useful for research applications that require the study of the caveolin-1 protein and its functional role.

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6 protocols using b6 cg cav1tm1mls j

1

Pathogen-free Murine Experimentation

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Animals were housed in pathogen-free animal facilities, and all experimental protocols were reviewed and approved per the Institutional Animal Care and Use Committee at the University of Nebraska Medical Center/University of Nebraska at Omaha (IACUC# 13-056-08-EP). C57Bl/6J and B6.Cg-Cav1tm1Mls/J mice were purchased from the Jack-son Laboratory (Bar Harbor, ME, USA). Post-natal day 54 (±5 days) mice were used for all experiments.
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2

Cav1-Null and BTBR Acallosal Mouse Models

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All animal procedures were performed in accordance with the Harvard University animal care committee’s regulations. Cav1-null mice on a congenic C57/Bl6 background (B6.Cg-Cav1tm1Mls/J) were obtained from The Jackson Laboratory, strain number 007083 (RRID:IMSR_JAX:007083). The original targeted null mutation was generated by Michael Lisanti at The Albert Einstein College of Medicine. A 2.2-kb region of the gene including exons 1 and 2 and a portion of the promoter region was replaced with a neomycin resistance cassette via homologous recombination (Razani et al., 2001 (link)).
BTBR acallosal mice on a congenic background (BTBR T+tf/J) were obtained from The Jackson Laboratory, strain number 002282 (RRID:IMSR_JAX:002282; Wahlsten et al., 2003 (link)). LP/J mice have been shown to be an appropriate callosal control population for BTBR mice. LP/J mice (LP/J) were obtained from The Jackson Laboratory, strain number 000676 (RRID:IMSR_JAX:000676).
C57/Bl6 wild-type (WT) mice were obtained from The Jackson Laboratory (RRID:IMSR_JAX:000664), and were used to breed with Cav1-null mice, and for birthdating and electroporation experiments. FEZF2 mutants were generated by Hirata et al. (2004 (link); GenBank accession number: AB042399).
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3

Caveolin-1 Knockout Mouse Model

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Experimentation was performed on mouse strains C57BL/6J (WT) from Harlan Blackthorn, UK and B6.Cg-Cav1tm1Mls/J (Cav1 KO) from Jackson Laboratories, Maine, USA. WT mice were backcrossed with Cav1 KO mice. Mice were aged between 10 and 24 weeks. All procedures were completed in compliance with Animals (Scientific Procedures) Act of 1986, and approved by the University of Manchester ethical committee. Mice had free access to food and water and were housed in a 12-hour light/dark cycle. All experiments were performed on mixed sex cohorts.
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4

Fetal Brain Development in Inbred Mice

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The inbred mice strains C57BL/6J (strain # 000664), AKR/J (strain # 00064), and B6.Cg-Cav1tm1Mls/J (strain # 007083) used in this study were purchased from the Jackson Laboratory (Bar Harbor, ME, USA). Approximately 8-week-old mice of these strains were used to establish timed pregnancies separately, as described previously [6 (link)]. The vaginal plug was observed to keep a record of the start of pregnancy (day 1). On days (d) 12, 15, and 17, the pregnant mice were euthanized, the fetuses were collected [15 (link)] and washed in sterile PBS, and the whole brain was dissected from each fetus [27 (link)].
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5

Genetically Modified Mouse Models

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Female C57BL/6J, B6.MRL-Faslpr/J (MRL/lpr, Fas-deficient), and B6.Cg-Cav1TM 1Mls/J (Cav-1 knockout) mice were purchased from the Jackson Laboratory (Bar Harbor, ME, United States) and Laboratory Animal Center of Sun Yat-sen University. Age-matched 8–10-week female mice from the same background were used in all experiments. All the animals were fed under specific pathogen-free conditions with an ambient temperature of 24°C, 55–65% relative humidity, and a 12:12 h light:dark cycle. Animal experiments were performed under protocols institutionally approved by Animal Care and Use Committee of Sun Yat-sen University (SYSU-IACUC-2021-000118).
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6

Dietary Fat and Caveolin-1 Impact

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The animal protocol was reviewed and approved by the Animal Care and Use Committee of the Iowa City Veterans Affairs Health Care System and complied with the Guiding Principles for Research Involving Animals and Human Beings. Beginning at 9 weeks of age, male C57BL/6J mice (wild type, WT) and mice deficient in caveolin‐1 (B6.Cg‐Cav1tm1Mls/J, Jackson Laboratories, stock #007083, cav‐1 KO) were randomly fed either normal mouse diet (low fat, LF, 13% kcal fat, 7001; Teklad, Harlan Labs, Madison, WI) or high saturated fat diet (HF, 60% kcal fat from lard, Research Diets, New Brunswick, NJ, D12492) for 12 weeks. To determine if a change in dietary fatty acids could reverse the effects of a high saturated fat diet, at the end of 12 weeks in a random group of mice on high‐fat diet, half of the kcal from lard was replaced with menhaden oil (MO, Research Diets, New Brunswick, NJ, D10122003) and the mice were maintained for an additional 6–10 weeks. Prior to terminal studies, body composition (nuclear magnetic resonance Bruker LF90II) was measured. For terminal study, mice were euthanized with ketamine/xylazine (100/10 mg/kg, ip), weighed, and tissues and serum obtained for measurement of vascular function, protein expression, glucose and lipid analysis.
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