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V1534

Manufactured by Ssniff
Sourced in Germany

The V1534 is a laboratory equipment designed for general scientific applications. Its core function is to provide accurate and reliable measurements or analysis for researchers and scientists. Specific details on its intended use are not available.

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18 protocols using v1534

1

Antibiotic-Induced Gut Microbiome Modulation in C57BL/6N Mice

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Specific pathogen free (SPF) C57BL/6 N mice were housed at 22  ±  1 °C and 50%–60% relative humidity, with a 12  h light–dark cycle as described previously in detail [5 (link)]. The mice were fed a chow diet (autoclaved, V1534, ssniff Spezialdiäten GmbH, Soest, Germany) ad libitum. For the antibiotic treatment, sole mice were fed a chow mash containing vancomycin (0.25 g/L) and metronidazol (1 g/L) (Sigma Aldrich, Steinheim, Germany) ad libitum for two days at the age of eight weeks, without any additional food (per group: male/female, 1/1). The control group received the same diet supplemented with water. The mouse experiment was performed according to the relevant ethical guidelines. The breeding and experimental use of the mice in the facilities at the Technische Universität München (School of Life Sciences Weihenstephan) was approved by the local institution in charge (Regierung von Oberbayern; approval number 55.2-1-54-2531-99-13 and 55.2-1-54-2532-17-2015).
For dietary intervention, the C57BL/6 N mice at the age of six weeks were fed for two weeks either a standard chow diet (5% grain–soybean-based crude fiber extract; V1534, ssniff) or a purified control diet with a comparable carbohydrate, fat, and protein content as chow, but with purified cellulose (5%) as the sole fiber source (autoclaved, S5745-E702, ssniff).
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2

Adipose Tissue Browning and Lipid Metabolism

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If not stated otherwise, all studies were performed in 8-12-wk-old SPF WT 129 SV/ev Tac (also termed 129S6 Sv/EV Tac) mice or UCP1 KO 129S1/SvImJ mice (male and female) (Li et al, 2014 (link)) fed a chow diet (V1534, Ssniff), housed at 23°C and 50-60% relative humidity with a 12 h light-dark cycle.
For adipose tissue browning studies, 10-wk-old SPF 129 SV/ev Tac male mice fed a chow diet (V1534, Ssniff) were housed at 4°C, 23°C, and 30°C for 7 d.
For short-term high-fat feeding studies, mice were fed an experimental control or HFD (Table S3) for 14 d.
To quantify de novo PC and PE synthesis via the Kennedy pathway, mice were supplemented simultaneously with choline (D9) and ethanolamine (D4) (each 1 mg/mouse; dissolved in 100 μl 0.9% NaCl solution) via intraperitoneal injection (i.p.) for 2 h, before PC (D9), PC (D4), and PE (D4) were analyzed in BAT, iWAT, and eWAT.
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3

Characterization of Wfs1-Deficient Rats

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For this study, outbred male CD® (Sprague-Dawley) IGS homozygous Wfs1-deficient (Wfs1-ex5-KO232) rats and their wild-type (WT) littermates (as controls) were used; outbred animals were selected as these are more representative of population-level heterogeneity. Wfs1-ex5-KO232 mutants have previously been extensively characterized [50 (link)]. Breeding and genotyping were executed at the Laboratory Animal Centre at the University of Tartu. Animals were housed in groups of 4 under a 12 h light/dark cycle (lights on at 7 a.m.) with unlimited access to food (Sniff universal mouse and rat maintenance diet, Ssniff #V1534, ssniff Spezialdiäten, Germany) and water. All experimental protocols were approved by the Estonian Project Authorization Committee for Animal Experiments (No 155, 6 January 2020), and all experiments were performed in accordance with the European Communities Directive of September 2010 (2010/63/EU). The study was carried out in compliance with the ARRIVE guidelines.
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4

Genotyping and Phenotyping of WFS1 Rat Model

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The generation and phenotype of a WFS1 mutant (Wfs1 exon 5 knock-out) rat has been described previously [3 (link)]. For this study, 3.5–4-month-old outbred CD® (Sprague-Dawley) IGS male homozygous Wfs1-deficient (Wfs1-ex5-KO232) and wild-type littermate (as a control) rats were used. The outbred rat line was chosen for better translational value. The breeding and genotyping were performed at the Laboratory Animal Centre at the University of Tartu. The animals were housed in cages, in groups of four animals per cage, under a 12 h light/dark cycle (lights on at 7 a.m.). The rats enjoyed unlimited access to food and water. Sniff universal mouse and a rat maintenance diet (Ssniff #V1534, ssniff Spezialdiäten, Germany) and reverse osmosis-purified water were used. The experiments were performed between 9 a.m. and 5 p.m. All the experimental protocols were approved by the Estonian Project Authorization Committee for Animal Experiments (No 165, 3 April 2020), and all the experiments were performed in accordance with the European Communities Directive of September 2010 (2010/63/EU). The study was carried out in compliance with the ARRIVE guidelines.
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5

Liver Analysis of Plin5 Knockout Mice

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C57BL/6 wild type (WT) and Plin5−/− mice were housed with 3–5 mice/cage. They were maintained at a constant temperature (20 °C) with a relative humidity of 50% and a 12 h of light and 12 h of darkness light cycle. All animals were fed ad libitum a normal chow (V1534, ssniff Spezialdiäten GmbH, Soest, Germany). All animals from which liver tissue was excised or primary cells were isolated were treated in full compliance with the guidelines for animal care and the protocols used were approved by the institutional German Animal Care Committee (LANUV, Recklinghausen, Germany; permit nos.: 84-02.04.2017.A268 and 81-02.04.2020.A228).
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6

Genetically Engineered Mice for Cancer Research

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Dro1−/− mice were generated as described previously [1 (link)]. Mice on the Dro1fl/fl background (in the following referred to as Dro1+/+ mice) were used as controls.
ApcMin/+ mice were purchased from the Jackson Laboratory and maintained on a C57BL/6J background. Mice were inspected on a daily basis and sacrificed when moribund.
Animals were housed under specific pathogen free conditions in a closed barrier system. All mice had access to water and to the same standard rodent diet (V1534, Ssniff, Soest, Germany) ad libitum. Experiments were carried out in accordance with the German Animal Welfare Act and with permission of the Government of Upper Bavaria (AZ55.2-1-54-2532-25-11 and AZ55.2-1-54-2532-48-2015).
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7

Metabolic Phenotyping of Plin5 Knockout Mice

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C57BL/6 wild type (WT) and Plin5−/− mice were housed 3–5 mice/cage. They were maintained at a constant temperature (20 °C) with a relative humidity of 50% and a 12 h of light and 12 h of darkness light cycle. WT (n = 24) and Plin5−/− (n = 22) mice were fed ad libitum for 30 weeks on a mouse normal chow (NC) composed of 58% carbohydrates, 33% protein and 9% fat (V1534, ssniff Spezialdiäten GmbH, Soest, Germany), or a HFD containing 40% fat, 20% fructose and 2% cholesterol (D17010102, Research Diets, Inc., New Brunswick, NJ, USA). Food intake and body weight of the animals were monitored twice and once weekly, respectively. All animals used in this study received humane care, and all animal protocols were in full compliance with the guidelines for animal care approved by the institutional German Animal Care Committee (LANUV, Recklinghausen, Germany; permit no.: 84–02.04.2017.A268).
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8

Age-related changes in mouse liver

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Animal experiments were approved by and conducted following national guidelines of the Ministry of Environment, Health and Consumer Protection of the federal state of Brandenburg, Germany (2347-44-2017) and institutional guidelines of the German Institute of Human Nutrition Potsdam-Rehbruecke, Germany. Mice were housed in polycarbonate cages and kept under diurnal 12 h light/dark cycles with light beginning at 6:30 AM; room temperature and humidity was kept constant at 22 °C and 55%, respectively. Food (V1534, Ssniff, Soest, Germany) and water were offered ad libitum.
Tissues were obtained from C57BL/6JRj mice of both sexes at an age of 24 (young adult, referred to as adult, 6 months) or 109–114 weeks (old adult, referred to as old, 28 months) anesthetised by isoflurane (Cp-pharma, Burgdorf, Germany), after blood withdrawal by heart puncture. Fresh liver tissue was cut in aliquots, snap-frozen in liquid nitrogen, and stored at −80 °C until further use. All analyses were conducted with samples that were fully blinded starting from the point of tissue harvesting.
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9

Abcb4 Knockout Mice Doxorubicin Study

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We repeated the Abcb4 knockout test using a different experimental design at the Saarland University Medical Center in Homberg, Germany. We obtained FVB.129P2-Abcb4tm1Bor/J and bred them to obtain 72 progeny (36 females and 36 males). We housed mice in individually ventilated cages (3 per cage) under standard conditions (12 hour light/dark cycle) and mice received water and a standard rodent diet (V1534, ssniff, Germany) ad libitum. Mice were divided by genotype into three groups of 24 mice each; wild type, heterozygous and homozygous knockout for Abcb4. We dosed 12 of the mice (6 males, 6 females) in each group with 0.9% saline solution and dosed the other 12 mice with 20 mg/kg of DOX; both were administered via tail vein injection. We collected blood from all mice five days after dosing and measured neutrophil counts on a Sysmex XE-5000 automated hematology analyzer. All animal experiments were approved by the respective government agency (Landesamt für Verbraucherschutz, Saarbrücken, Saarland;TV43/2012).
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10

Generation of Smarcd2-deficient Mice

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C57BL/6 ES cell clone 11930A-F4 carrying a mutant Smarcd2 allele was generated by Regeneron Pharmaceuticals and obtained from the KOMP repository (see URLs). To generate Smarcd2-deficient mice, clonal ES cells were injected into C57BL/6BrdCrHsd-Tyrc (albino) blastocysts and these were transferred to pseudo-pregnant NMRI foster mothers. The resulting chimeras were crossed to C57BL/6 albino mice to identify germline transmission of the targeted allele and to produce mice heterozygous for the mutation. F1 intercrosses of heterozygous mice resulted in smarcd2+/+, smarcd2+/−, and smarcd2−/− embryos, which were genotyped using standard PCR reaction conditions (Supplementary Fig. 7 and Supplementary Table 3).
Animals were maintained under specific-pathogen-free conditions at 23 °C, 65% humidity with a 12-h light/12-h dark cycle and had free access to a standard rodent diet (V1534, Ssniff) and water. All animal experiments were carried out in accordance with the German Animal Welfare Act with permission from the responsible veterinary authority.
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