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71 protocols using c57bl 6j

1

Avertin and 3MIX Effects in Obese Mice

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Male and female C57BL/6J and ICR mice aged six weeks were purchased from Japan SLC
(Hamamatsu, Japan).
All animals in this study were housed in individual cages and were maintained on a
12-hour light/dark cycle with lights on at 7 AM. The mice were fed a HFD (HFD32, CLEA
Japan, Osaka, Japan) or standard diet (CE7, CLEA Japan), which served as the control, for
eight (males) or 12 weeks (females). Thus, 14-week-old male mice and 18-week-old female
mice were used for the experiment, and the effects of avertin were compared.
For comparison of the effects of avertin and 3MIX, female C57BL/6J mice, aged six weeks,
were purchased from Japan SLC and fed HFD for 14 weeks. Thus, 20-week-old female mice were
used for this experiment. All animals in this study were housed in individual cages. All
experimental procedures and animal care were carried out according to the relevant
guidelines and regulations and were approved by the Fukushima Medical University Institute
of Animal Care and Use Committee.
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2

Generation and Characterization of Dcir Knockout Mice

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Dcir–/– mice [11 (link)] were
backcrossed to C57BL/6J (Japan SLC, Japan) over twelve generations. Age- and
gender-matched WT C57BL/6J mice were purchased from Japan SLC. All mice were kept under
specific pathogen–free conditions in environmentally controlled clean rooms at the Center
for Experimental Medicine and Systems Biology, the Institute of Medical Science, the
University of Tokyo, and Research Institute for Biomedical Sciences, Tokyo University of
Science. All animal experiments were approved by the committees for animal experiments of
both universities and conducted according to the institutional ethical guidelines for
animal experiments and the safety guidelines for gene manipulation experiments.
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3

Generation and Utilization of IFNAR2-/- Mice

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C57BL/6J (wild-type, WT) mice were purchased from Japan SLC (Hamamatsu, Japan) and IFNAR2−/−mice (C57BL/6J background) were established as described previously [21 (link)]. All mice were housed in an animal facility under specific pathogen-free conditions and used at 7-8 weeks of age. All animal experimental procedures used in this study were performed in accordance with the institutional guidelines for animal experiments at Osaka University and the National Institute of Biomedical Innovation.
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4

Social Defeat Stress in Mice

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Male C57BL/6J and ICR mice were obtained from Japan SLC, Inc. Juvenile, male C57BL/6J mice (3 weeks old) were used to exposure to social defeat stress. Aggressive, male ICR mice (over 7 weeks old) for social defeat stress were screened based on the duration of attacks on C57BL/6J mice, with more than 1/10 minutes as the inclusion criterion. Unfamiliar target male ICR mice (over 4–6 weeks old) were used for the social interaction test. They were housed in plastic cages in a regulated environment (23°C ±1°C, 50±5% humidity), with a 12-hour-light/-dark cycle (lights on at 9:00 am). Food (CE2; Clea Japan Inc.) and tap water were available ad libitum. All experiments were conducted in accordance with the Guidelines for Animal Experiments of the Nagoya University Graduate School of Medicine. Procedures involving animals and their care were conformed to the international guidelines set out in the National Institutes of Health’s Guide for the Care and Use of Laboratory Animals (NIH Publications No. 8023, revised 1978).
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5

Mechanical Overload Experiments in Mice

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The C57BL/6J and CD2F1 mice were purchased from the Japan SLC and Charles River Laboratories Japan, respectively. Mice were housed in cages with a constant temperature (24 °C) and a 12-h light:12-h dark cycle and were provided with water and food ad libitum, except during the fasting experiments. Animal experiments were conducted under protocols approved by the Institutional Animal Care and Use Committee of Fujita Health University, Japan (#AP16055, approved on June 24th, 2016). Mechanical overload experiments were approved by the Animal Care and Use Committee of the National Cerebral and Cardiovascular Center in Japan (#16035, approved on March 28th 2016) and were conducted under institutional and national guidelines. All animal experiments were performed in accordance with the ethical standards laid down in the 1964 declaration of Helsinki and its later amendments.
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6

Mouse Embryo Implantation Protocols

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ICR and C57BL/6J mice were purchased from Japan SLC (Hamamatsu, Japan). They were bred under the controlled condition (temperature 22 ± 2°C, humidity 50 ± 10%, and 12–12 hr light-dark
cycle) with water and food ad libitum. After 1-week acclimation, eight to ten-week-old virgin mice were paired in syngeneic in the evening. On the next morning, the mice
confirmed vaginal plugs were designated as day 0.5 of pregnancy (D0.5).
ICR mice were euthanized by cervical dislocation after deep anesthesia by isoflurane. More than three pregnant mice were used at each time point and more than five pregnant implantation
sites were collected from each pregnant mouse. Specimens were fixed in 10% neutral-buffered formalin for histological studies. Other samples were stored by rapid freezing for quantitative
PCR and western blot.
All mice used in this study were kept under veterinary health control and received care along with the guideline for the proper implementation of animal use at the Yamaguchi University.
Experimental designs were passed preliminary reviews by the Ethical Committee on Animal Experimentation at Yamaguchi University (Approval numbers: 361 and 443).
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7

Muscle Atrophy Induction in Mice

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Mice (C57BL/6J and CD2F1) were purchased from the Japan SLC and Charles River Laboratories Japan. Mice were housed in cages with a constant temperature (24 °C) and a 12 h light: 12 h dark cycle and were provided water and food ad libitum. During the fasting experiments, no food intake was allowed. C57BL/6J mice were used for denervation, atrophy by casting and fasting, and CD2F1 mice were used for cachexia treatment. The detailed protocols for each muscle atrophy experiment and the changes in the skeletal muscle weight were described previously [23 (link)].
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8

Mouse Brain Development and Medaka Fish

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Mice (C57/BL6J) were obtained from Japan SLC (Hamamatsu, Japan) and brain samples were prepared at different stages: embryo 14.5 days (E14.5), postnatal day 1 (P1), P15, P30, and P45. The Nagoya strain of medaka fish, Oryzias latipes, was used as the wild type (WT). Wild type medaka strain was supplied by the National Bioresource Project (NBRP) Medaka. Fish stocks were maintained in 16-L tanks with a circulating water system maintained at 26 °C and a 14 h light/10 h dark cycle. The development and phenotype of medaka fish were observed using an SZX12 DP80 microscope (Olympus, Tokyo, Japan).
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9

Murine Cancer Models and Tranilast Treatment

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Female C57BL/6J and SCID mice aged 6 weeks were purchased from Japan SLC (Hamamatsu, Japan) and CLEA Japan (Tokyo, Japan), respectively. The mice were maintained under specific pathogen-free conditions. All mouse experiments were carried out in compliance with the Guidelines for Animal Experimentation from Shiga University of Medical Science (Shiga, Japan).
The mouse lymphoma cell line E.G7 that expresses ovalbumin (OVA) and the natural killer (NK) cell-sensitive cell line YAC-1 were purchased from ATCC (Manassas, VA, USA), and were passaged for fewer than 6 months. The mouse Lewis lung carcinoma cell line LLC1 and the mouse melanoma cell line B16F1 were provided by the Cell Resource Center for Biomedical Research, Tohoku University (Sendai, Japan).
Tranilast (N-[3,4-dimethoxycinnamoyl]-anthranilic acid) (Sigma-Aldrich, St. Louis, MO, USA) was dissolved in DMSO at a concentration of 25 mM as a stock solution.
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10

Mice Protocols for Cell Culture

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Mice (C57BL/6J for injection experiments and Jcl:ICR for primary-cultured cells) were obtained from Japan SLC. All experimental protocols were performed according to the recommendations of the Animal Care and Use Committee of Tokyo Metropolitan Institute of Medical Science, and all animal experiments were carried out in accordance with ARRIVE guidelines (The ARRIVE guidelines 2.0). All experimental protocols were approved by the Animal Care and Use Committee of Tokyo Metropolitan Institute of Medical Science (approval number 21-037).
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