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S4207

Manufactured by Bio-Serv

The S4207 is a laboratory centrifuge designed for general-purpose applications. It is capable of separating liquids and solid-liquid mixtures at high speeds. The centrifuge has a maximum rotor speed of 4,207 RPM and can accommodate various rotor and sample configurations.

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5 protocols using s4207

1

Corticosterone and Doxycycline Treatment Protocol

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CORT was prepared as previously described (David et al., 2009 (link)). Specifically, 35 μg/mL (equivalent to 5 mg/kg/day) CORT (27840; Sigma-Aldrich, St. Louis, MO, USA) was dissolved in 0.45% 2-hydroxypropyl cyclodextrin (332593; Sigma-Aldrich) and delivered in lightproof bottles, available ad libitum in drinking water. Control mice received 0.45% β-cyclodextrin in drinking water (C4767; Sigma-Aldrich). DOX was provided in chow containing 200 mg/kg DOX (S3888; Bioserv, Flemington, NJ, USA) fed ad libitum throughout life. Control chow (S4207; Bioserv) was used when DOX was withdrawn from the diet.
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2

Corticosterone and Doxycycline Treatment Protocol

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CORT was prepared as previously described (David et al., 2009 (link)). Specifically, 35 μg/mL (equivalent to 5 mg/kg/day) CORT (27840; Sigma-Aldrich, St. Louis, MO, USA) was dissolved in 0.45% 2-hydroxypropyl cyclodextrin (332593; Sigma-Aldrich) and delivered in lightproof bottles, available ad libitum in drinking water. Control mice received 0.45% β-cyclodextrin in drinking water (C4767; Sigma-Aldrich). DOX was provided in chow containing 200 mg/kg DOX (S3888; Bioserv, Flemington, NJ, USA) fed ad libitum throughout life. Control chow (S4207; Bioserv) was used when DOX was withdrawn from the diet.
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3

Inducible Adipocyte-Specific p53 Knockout

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p53-iAKO mice were generated by breeding Doxycycline-inducible (TRE-Cre) (JAX stock #006234), adipocyte-specific (Adipoq-rtTA, a kind gift from Dr. Scherer) (Sun et al., 2012 (link); Wang et al., 2013 (link)), and floxed-Trp53 (JAX stock #008462) mouse lines together. Adipocyte-specific p53-knockout can be induced by Doxycycline-diet feeding (BioServ, #S3888, Doxycycline 200 mg/kg, sterile, #S4207 control diet, 20.8% protein, 8.7% fat, 2.1% fiber, 3.75 kcal/gm) from weaning until 6–10 weeks old. After 2 weeks Doxycycline feeding, the diet was replaced by regular food in animal facility, and proceeded to the experiments as indicated.
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4

Xenograft Tumor Growth Regulation

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Xenograft tumor experiments were approved by the Animal Care and Use Committee at the University of Pennsylvania. Briefly, ten female NSG mice (the Jackson Laboratory, 6 weeks, 005557) were injected subcutaneously into both flanks with 2 million LPS246 cells stably expressing TetO-FBP2. Before injection, cells were resuspended in 100 μl PBS mixed with an equal volume of Matrigel (Corning, 356234). Once palpable tumors were established, tumor volume was measure with a digital caliper. When the average tumor size reached 100 mm3, ten mice were randomly separated into two groups: (1) Doxycycline diet (Bio-Serv, S3888) and (2) control diet (Bio-Serv, S4207). Upon completion of the experiment, the animals were sacrificed by CO2 inhalation and xenograft tumors were dissected for downstream analyses. Mice were housed in a controlled environment (12 h light/12 h dark cycle, humidity 30~70%, temperature 20~22°C), and had free access to water and rodent diet. All animal experiments were performed in accordance with the Guide for Care and Use of Laboratory Animals of the NIH. All animal studies were approved by Institutional Animal Care and Use Committee Office of Animal Welfare of University of Pennsylvania.
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5

Doxorubicin Inhibits Tumor Growth

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H3118-fusion ishRNA cells (1 × 106) were mixed with 100 μL of Matrigel (BD Biosciences , 354230)/PBS (Thermo Fisher Scientific, 10010-023) (1:1) and injected s.c. into the right flank of 8- to 12-week-old NOD/SCID mice (The Jackson Laboratory). Mice were randomly separated into 2 groups and fed with control diet (Bio-Serv, S4207, n = 5) or 200 mg/kg Dox chow diet (Bio-Serv, S3888, n = 6) immediately after the implantation of tumor cells. In a second experiment, mice were provided with control diet (n = 5) or Dox chow when the volumes of xenografts reached approximately 50 mm3 (n = 6) or approximately 100 mm3 (n = 6) after implantation. The tumors were measured daily with a Dial caliper and tumor volumes were calculated based on this formula: tumor volume = (length × width2) × 0.5.
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