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Male c57bl 6 mice

Manufactured by Samtako Bio
Sourced in Cameroon

Male C57BL/6 mice are a commonly used laboratory mouse strain. They are rodents of the species Mus musculus.

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15 protocols using male c57bl 6 mice

1

Amlexanox Modulates LPS-Induced Inflammation

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Seven-week-old C57BL/6 male mice were purchased from Samtako (South Korea). Mice were maintained under standard conditions (24 ± 2 °C, 12 h day-night cycle, 50 ± 5% humidity) in a pathogen-free environment. Mice were allowed free access to food pellets and water throughout the study period. Experimental procedures and animal management procedures were approved by the Institutional Animal Care and Use Committee (IACUC) of Jeonbuk National University in Korea (approval number: NON2023-111). All methods were conducted following IACUC ethical guidelines and regulations supported by the Korean Council on Animal Care and Korean Animal Protection Law, 2007; Article 13 (Experiments with animals). All animal trials followed the ARRIVE 2.0 guidelines, including study design, animal numbers, randomization, and statistical methodologies.
Twenty-four WT mice were divided into 4 groups: the PBS group (n = 5), the amlexanox-only control group (n = 5), LPS positive control (n = 7), and the amlexanox plus LPS group (n = 7).WT mice were injected with amlexanox (50 mg/kg-i.p) or PBS as a control daily for 3 days and thereafter, injected with LPS (10 mg/kg) (Escherichia coli O111:B4 was obtained from Sigma-Aldrich, St. Louis, MO, USA) for 24 h. Figure 1A depicts the drug treatment schedule.
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2

Induction of Liver Injury in Mice

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For induction of liver injury, 8-week-old C57BL/6 male mice (20–25 g; Samtako, Osan, Korea) were selected. Male C57BL/6 mice were fed a control diet or a DDC supplemented diet (0.1%) for 4 weeks to induce advanced biliary fibrosis as previously described (15 (link)). All animal protocols were approved by the Institutional Animal Care and Use Committee of Catholic University of Daegu (Daegu, Korea). The mice received an intraperitoneal injection of apamin (0.1 mg/kg) dissolved in saline twice a week. Mice were sacrificed after 4 weeks from the first DDC diet administration.
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3

Murine Model for Biomedical Research

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C57BL/6 male mice, 6 weeks old, body weight (BW) 22 ± 2 g were purchased from Samtako Inc. (Osan, Republic of Korea). The mice were housed under a humidity of 50 ± 5%, a temperature of 23 ± 1 °C, a 12 h/12 h light and dark cycle, and were provided free access to a standard diet and tap water. All mice were provided with proper care following the guidelines of the Institutional Animal Care and Use Committee (IACUC) of the Korea Institute of Oriental Medicine (KIOM; Daegu, Republic of Korea), who reviewed and approved this study (IACUC-KIOM-D-18-013).
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4

Evaluating TGF-β1/Smad ODN Transfection in Chronic Liver Injury

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Male C57BL/6 mice (6 weeks old, 20–22 g; Samtako) were housed in a room with controlled humidity and temperature, and a 12-hr light-dark cycle. All experiments were performed in accordance with the ethical guidelines of Institutional Animal Care and Use Committee of the Catholic University of Daegu (EXP-IRB number: 2014-0001-CU-AEC-04-A). To examine the in vivo transfection efficiency of synthetic TGF-β1/Smad ODN, FITC-labeled TGF-β1/Smad ODN was injected into mice via the tail vein. The mice were killed 24 hr after injection. Liver tissues were frozen with OCT compound (Sakura Finetek Japan). Cryosections of liver, which were transferred with FITC-labeled TGF-β1/Smad ODN, were examined using fluorescence microscopy.
Chronic liver injuries were induced by intraperitoneal injections of CCl4 (2 mL/kg, dissolved in corn oil [1:3 ratio]) three times a week.42 (link), 73 (link) One week after the first CCl4 injection, either Scr ODN or TGF-β1/Smad ODN (10 μg) was transferred biweekly via the mouse tail vein, using an in vivo gene delivery system (Mirus Bio). Mice were killed 8 weeks after the first CCl4 injection.
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5

Neuroprotective Therapy Evaluation in Rodents

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Male SD rats (300 ± 10 g), male C57BL/6 mice (25 ± 1 g), and male Wistar rats (180 ± 10 g) were purchased from Samtako Inc. (Osan, Korea). Animals were housed in a facility with constant humidity (60 ± 10%), temperature (23 ± 1 °C), and a 12-h light/dark cycle (lights on at 7 am). Food and water were available ad libitum throughout the study. Animals were acclimatised to laboratory conditions for at least 1 week before undergoing surgery. Analgesics, such as opioids and nonsteroidal anti-inflammatory drugs, were not administered during the postoperative phase because they may interfere with the assessment of the neuroprotective therapies83 (link). All experimental procedures were performed according to the Principles of Laboratory Animal Care (National Institutes of Health publication, #85–23, revised in 1985). The experimental protocols were approved the Institutional Animal Care and Use Committee of Korea Institute of Science and Technology for Eastern Medicine (approval no. KISTEM-IACUC-2017-004).
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6

Unilateral Ureteral Obstruction Mouse Model

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Male C57BL/6 mice (Samtako, Osan, Korea), 8 weeks of age, had free access to standard food and water throughout the experiments. Mice were anesthetized with an intraperitoneal injection of pentobarbital sodium (50 mg/Kg). After a left flank incision, left ureter was isolated and ligated with 6–0 silk to make UUO model. Control group of mice underwent sham operation, which was identical to that of UUO group, except the ligation of the ureter. The experimental protocols for animal models were reviewed and approved by the boards of the Kyungpook National University and Kyungpook National University Hospital (KNU-2015-0041).
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7

Ethanol-Induced Brain Injury in Mice

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Male C57BL/6 mice (4 weeks old, n = 15; n = 5 for mitochondrial tests, n = 7 for in vivo and ex-vivo tests, n = 3 for Western blot assay) were purchased from Samtako (Osan, Republic of Korea). The mice were placed in groups consisting of 3–4 animals per cage and housed under the conditions of 12/12 h light/dark cycles at 22 ± 2 °C. Mice were assigned to 4 groups: control group, ethanol group, and FPB 50 (50 mg/kg of body weight) and FPB 100 (100 mg/kg of body weight) groups. FPB and ethanol groups were treated with FPB or drinking water by oral gavage, respectively. After 30 min, 5 g/kg body weight of 25% (v/v) ethanol was orally administered except for the control group. After 8 weeks, mice were anesthetized by exposure to CO2 gas, and then blood samples and brain tissues were collected. All animal study procedures were approved by the Institutional Animal Care and Use Committee (IACUC) of Gyeongsang National University guidelines (Certificate No. GNU-220710-M0079) on 10 July 2022.
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8

Effect of mTOR/STAT3 Modulation on Renal Fibrosis

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Male C57BL/6 mice (6 weeks old, 20–22 g; Samtako, Daejeon, South Korea) were housed individually in cages and maintained at a set temperature (22 ± 2 °C) and humidity (55%) with a 12 h light–dark cycle. After 1 week of acclimatization, the mice were randomly divided into five groups (n = 7 per group) as follows: (1) an untreated group (normal control, NC); (2) injected with the mTOR/STAT3 synthetic ODNs group (mTOR/STAT); (3) UUO surgery group (UUO); (4) underwent UUO surgery and were injected with the scrambled ODNs group (UUO+Scr); (5) underwent UUO surgery and were injected with the mTOR/STAT3 synthetic ODNs group (UUO+mTOR/STAT). For UUO surgery, each mouse was anesthetized, its abdominal cavity was incised, and the left ureter was ligated with 5–0 silk suture at both the distal and the proximal locations. The synthetic ODNs (10 μg) were injected into the mice intravenously at 2 days before ureteral ligation and 2 and 5 days after the UUO surgery. One week after the UUO operation, the mice were sacrificed. Figure 1B shows the design of the animal experiment. The animal protocols were approved by the Institutional Animal Care and Use Committee of the Catholic University of Daegu (EXP-IRB number: DCIAFCR-190620-07-Y).
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9

Murine C57BL/6 Model Protocols

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Male C57BL/6 mice were purchased from Samtako (Korea). The Institutional Animal Care and Use Committee of Konyang University approved the animal care protocol for the experiments performed in the study.
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10

C57BL/6 Mouse Housing Protocol

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Male C57BL/6 mice (8–10 weeks old; Samtako, Gyeonggi-do, Korea) were maintained in our facility under normal conditions (12-h light/dark cycle, temperature, 23°C ± 2°C). All animal protocols conformed to international laws and National Institutes of Health policies, including the Care and Use of Laboratory Animals (National Institutes of Health publication no. 85-23, 1985, revised 1996). All experimental procedures were performed according to the Guidelines for the Care and Use of Laboratory Animals of Jeju National University (permission no.: 2022-0062).
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