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The H10010 is a laboratory centrifuge designed for general-purpose applications. It is capable of separating components of a liquid mixture based on their relative densities and sizes. The centrifuge can be used to isolate cells, proteins, or other biomolecules from complex samples.

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8 protocols using h10010

1

Dietary-induced NAFLD in C57BL/6J Mice

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Six-week-old C57BL/6J mice were housed in a specified pathogen-free animal room with a 12-h light/12-h dark cycle and free access to food and water. For diet-induced NAFLD, 6-week-old male C57BL/6J mice were randomized into two groups: one group was fed a HFD (60.9% fat, 21.8% carbohydrate, and 18.3% protein; H10060) for 16 weeks, and the other group was fed a normal chow diet (NCD) (4% fat, 78% carbohydrate, and 18% protein; H10010, HFK Bioscience, Beijing, China). Gene-edited ob/ob mice provided by HFK Bioscience (Beijing, China) were fed an NCD for 8 weeks. The mice were sacrificed at the time point, blood samples were collected for testing, and liver tissue was collected for fixation with paraformaldehyde or storage with frozen liquid nitrogen. All experimental procedures in this study were approved by the Animal Use Subcommittee of Tongji Medical College of Huazhong University of Science and Technology.
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2

Generating NAFLD Mouse Model with Bcl6

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B6.129S (FVB)-Bcl6tm1.1Dent/J(Bcl6fl/fl) were obtained from the Jackson Laboratory (Stock No.: 023727). Alb-Cre mice were obtained from the Model Animal Research Center of Nanjing University. Alb-Cre mice were bred with the Bcl6 fl/fl mice to obtain the Alb-Cre Bcl6Δ mice. Genotyping was performed via PCR using previously published protocols [28 (link)–30 (link)]. The Animal Use Subcommittee of Tongji Medical College of Huazhong University of Science and Technology approved all animal experimental procedures. A specific-pathogen-free facility equipped 12-h light/12-h dark cycles and free access to food and water were used to house six-week-old C57BL/6J mice.
Six-week-old male mice were randomized into two groups to create diet-induced NAFLD – the first of these groups were fed 16 weeks of normal chow diet (NCD) (4% fat, 78% carbohydrate, and 18% protein; H10010, HFK Bioscience, Beijing, China) while the other group received 16 weeks of HFD (60.9% fat, 21.8% carbohydrate, and 18.3% protein; H10060). NCDGene-edited ob/ob mice provided by HFK Bioscience (Beijing, China) were fed NCD for 8 weeks. After this duration, mice were sacrificed, blood samples were harvested, and livers were dissected for immediate paraformaldehyde fixation or storage for further use with frozen liquid nitrogen.
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3

Phenotypic Analysis of Lewis Rats

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Lewis homozygous (dw/dw) rats were provided by Professor Michael J Waters, University of Queensland, Australia. Lewis wild-type (WT) rats were purchased from Beijing Vital River Laboratory Animal Technology Co., Ltd. (Beijing, China). Lewis heterozygote (dw/+) rats were generated by mating Lewis dw/dw and Lewis WT rats. Lewis dw/dw rats at 37 weeks (five females and five males), and Lewis dw/+ rats at 37 weeks (five females and five males) were analyzed in our study. The rats were housed in a standard 12h light/dark cycle environment with sufficient water and food (SF; 10% kcal fat, H10010, Beijing HFK Bioscience Co., Ltd., Beijing, China). The rats were in narcotism by injecting 2.5% tribromoethanol into the cavum abdominis (15 mL/kg). All rats were weighed before sacrifice. The body lengths were measured from the nose’s tip to the tail’s tip after sacrifice. The intact livers were collected and then weighed. The ethics committee of Peking Union Medical College Hospital approved the animal experiment protocols (XHDW-2021-035).
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4

High-Fat Diet Induced Obesity Study

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Male ICR mice (8 weeks‐of‐age, weighing 25–27 g; Beijing HFK Bioscience Co., Ltd, Beijing, China) were randomly assigned to two groups, which were fed with HFD (n = 25) and standard food (SF, n = 10) for 8 weeks, respectively. The SF (H10010, 10% kcal fat) and HFD (H10045, 45% kcal fat) were purchased from Beijing HFK Bioscience Co., Ltd. The compositions of the diets are shown in Table S1. Mice fed with HFD were then randomly divided into the SY group (n = 12) and HFD group (n = 13). The mice were housed in a temperature‐controlled room (21–23°C) with a 12‐h light–dark cycle, and had free access to water and food. Mice were intraperitoneally injected with 120 mg/kg SY daily in the SY group, and with the same volume of saline in the HFD and SF groups. The bodyweight of mice was recorded weekly. The animal experiments were carried out according to the NIH Guide for the Care and Use of Laboratory Animals. The experimental protocol was approved by the ethics committee of Peking Union Medical College Hospital.
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5

High-Fat Diet Feeding and Metabolic Assessment

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After 3 days of adaptive feeding, mice were randomly divided into 2 groups, CD and HFD groups. Mice in CD and HFD groups were fed a control standard diet [20% kcal protein, 70% kcal carbohydrate and 10% kcal fat, H10010, Beijing HFK BIOSCIENCE CO.,LTD.) or high-fat diet (20% kcal protein, 20% kcal carbohydrate and 60% kcal fat, H10060, Beijing HFK BIOSCIENCE CO.,LTD.)], respectively. Body weights were measured once a week. After 8 weeks of feeding, mice were randomly selected from the CD group and HDF group for examination via glucose tolerance test (GTT), insulin tolerance test (ITT), fasting blood glucose (FBG), HOMA-IR, and serum insulin levels to establish the model.
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6

Dietary Intervention and Metabolic Reprogramming

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Previous studies have shown strong causative relation between restricted intrauterine growth and adult metabolic reprograming in rodents (17 (link), 18 (link)). To reduce the potential impact of uneven intrauterine nutrition accompanied by different litter size, we used a previously developed ICR mouse model (19 (link)). Adult (6- to 8-week-old) male and female ICR mice were purchased from Beijing Vital River Laboratory Animal Technology Co., Ltd. and caged. Three-week-old pups were weaned and randomly assigned to insulin resistance (IR) and control (Con) group. Respectively, they were fed ad libitum for 19 weeks with either high fat diet (n = 9) composed of 60% Kcal from fat (Beijing HFK Bioscience Co., LTD., H10060) to induce IR or standard chow diet (n = 12, Beijing HFK Bioscience Co., LTD., H10010). All mice were maintained on a 12 h-light/12 h-dark cycle in a specific pathogen-free barrier facility. Mice were fasted overnight before sacrifice. Liver, epididymal fat, quadriceps femoris and gastrocnemius were collected, shock-frozen in liquid nitrogen and stored at −80°C. All animal experiments were performed with the approval of the Animal Ethics Committee of Hebei General Hospital.
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7

Evaluating High-Fat Diet Effects in Mice

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Male 7-week-old C57BL/6J mice were purchased from Beijing Vital River Laboratory Animal Technology Co., Ltd. (Beijing, China), and housed in a standard 12-h light/dark cycle with free access to food and water. After 1 week of acclimation, mice were randomly assigned to a standard food (SF; 10% kcal fat, n=20; H10010, Beijing HFK Bioscience Co., Ltd., Beijing, China) group and a high-fat diet (HFD; 45% kcal fat, n=30; H10045, Beijing HFK Bioscience Co., Ltd., Beijing, China) group. The compositions of the experimental diets are shown in Table S1. Ten weeks later, mice fed with SF were divided into SF-Saline group (n=10) and SF-SY group (n=10), and mice fed with HFD were weighed and divided into HFD-Saline group (n=10), HFD-SY group (n=10), and HFD-HSYA group (n=10). Mice in the SY and HSYA intervention group were intraperitoneally injected with 200 mg/kg/d SY or HSYA for ten weeks, and mice in SF-Saline and HFD-Saline groups were intraperitoneally injected with equal volume of saline. Body weight was recorded twice a week, and food intake was recorded weekly. The animal experiment protocols were approved by the ethics committee of Peking Union Medical College Hospital.
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8

High-Fat Diet-Induced Obesity Model

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Male C57BL/6J mice were purchased from the Beijing Vital River Laboratory Animal Technology Co., Ltd. (Beijing, China). The mice were housed in a 12 h dark/ light cycle environment at the age of seven weeks and had free access to food and water. After one week of acclimation, mice were randomly placed on a standard food (SF; 10% kcal fat, n = 10; H10010, Beijing HFK Bioscience Co., Ltd., Beijing, China) or a HFD (45% kcal fat, n = 20; H10045, Beijing HFK Bioscience Co., Ltd., Beijing, China), and maintained on the same diet for 20 weeks. The mice fed with HFD were randomly divided into the HFD and the HFD-Liraglutide groups. Then, the mice in the HFD-Liraglutide group were subcutaneously injected with 200 μg/kg/d Liraglutide (15676, Novo Nordisk, Denmark) for 20 weeks, while the SF group and the HFD group were intraperitoneally injected with equal volumes of saline. The body weight of mice was recorded twice a week and food intake was recorded weekly. All the experimental animal procedures were approved by the ethics committee of Peking Union Medical College Hospital (XHDW-2017-001).
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