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The RL-95 is a laboratory centrifuge designed for general-purpose applications. It features a direct-drive motor and a microprocessor-controlled digital display for precise speed and time control. The RL-95 can accommodate various rotor sizes and configurations to handle a wide range of sample volumes.

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5 protocols using rl 95

1

Establishment and Maintenance of Endometrial Cancer Cell Lines

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Human EC cell lines Ishikawa, HEC-1A, RL-95, and AN3CA were obtained from Zhong Qiao Xin Zhou Biotechnology Co., Ltd (Shanghai, China), and KLE cells were purchased from Procell Life Science & Technology Co., Ltd (Wuhan, China). All the above cell lines were recently authenticated by using short tandem repeat (STR) analysis. Ishikawa cells were maintained in Dulbecco’s modified Eagle’s medium (DMEM; BI, Beit-Hamek, Israel). HEC-1A cells were cultured in McCoy’s 5A medium (Gibco, Carlsbad, USA) with 1% sodium pyruvate solution. RL-95 cells were cultured in DMEM-F12 (Gibco) with 1% sodium pyruvate solution and 5 μg/mL insulin. AN3CA cells were cultured in Minimal Essential Medium (MEM; Gibco) with 1% sodium pyruvate solution and 1% non-essential amino acid solution. KLE cells were cultured in DMEM-F12. All the media contained 10% fetal bovine serum (v/v) and 1% penicillin-streptomycin (v/v), and all the cells were cultured in an incubator containing 5% CO
2 at 37°C. The compound TSI-01 was purchased from APExBio Company (Houston, USA).
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2

Endometrial Carcinoma Cell Culture

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Endometrial carcinoma cell lines HEC-1-B, RL-95 and KLE were purchased from ATCC and Ishikawa was purchased from Sigma-Aldrich. Cells were obtained directly from the cell banks, which perform cell line characterizations and passaged in the authors' laboratory for fewer than 6 months after resuscitation. HEC-1-B cell line was maintained in MEM (Gibco) supplemented with 10% fetal bovine serum (FBS), Ishikawa cell line was cultured in MEM (Gibco) supplemented with 5% FBS and KLE and RL-95 were maintained in DMEM (Gibco) supplemented with 10% FBS. All cell lines were maintained with supplementation of 2% penicillin/streptomycin and incubated in humidified chamber at 37°C in 5% CO2 atmosphere.
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3

Culturing Human Endometrial Cell Lines

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Human endometrial cancer cell lines (Ishikawa, RL95 and HEC-1) and a human normal endometrial fibroblast cell line HESC were purchased from the American Type Culture Collection (ATCC, Manassas, VA). Dulbecco’s modified Eagle’s medium/nutrient mixture F-12 (DMEM/F12, Sigma-Aldrich, St. Louis, MO, USA) supplemented with 10% fetal bovine serum (FBS, Thermo Fisher Scientific, Waltham, MA, USA) was used to culture Ishikawa, RL95, HEC-1, and HESC cells. All cell lines were maintained in a humidified 5% CO2 incubator at 37°C.
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4

Culturing Trophoblast and Endometrial Cells

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The two trophoblastic human cell lines JEG-3 and BeWo, as well as the epithelial endometrial cell line RL-95, were purchased from the American Type Culture Collection (ATCC, Manassas, VA, USA) and maintained under standard culture conditions in 5% CO2 at 37 °C. The culture media used were Dulbecco’s modified Eagle’s medium (DMEM) F12 (Thermo Fisher Scientific, Waltham, MA, USA) for the BeWo and RL-95 cells, and DMEM (Thermo Fisher Scientific) for the JEG-3 cells. Each medium was supplemented with 1% penicillin–streptomycin (P/S; Biowest, Nuaillé, France) and 10% fetal bovine serum (FBS; PAN-Biotech, Aidenbach, Germany).
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5

Culturing Human Endometrial Cancer Cell Lines

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Human EC cell lines (HEC-1A, Ishikawa, RL-95 and An3C cells) were purchased from the Cell Bank of the Chinese Academy of Sciences (Shanghai, China). HEC-1A cells were cultured in McCoy’s 5A medium (Thermo Fisher Scientific Inc., Waltham, MA, USA) supplemented with 10% fetal bovine serum (FBS) (Biological Industries, Kibbutz Beit-Haemek, Israel) and 1 mM sodium pyruvate (Thermo Fisher Scientific Inc.). Ishikawa and An3C cells were grown in RPMI 1640 medium (Thermo Fisher Scientific Inc.) with 10% FBS. RL-95 cells were maintained in DMEM/F12 medium (Thermo Fisher Scientific Inc.) with 10% FBS. All cell culture media were supplemented with 100 U/ml penicillin and 100 μg/ml streptomycin (Thermo Fisher Scientific Inc.). Cells were cultured at 37 ℃ in a 5% CO2 atmosphere. For in vitro experiments, BET inhibitors were added to cultured cancer cells at indicated concentrations. Equivalent concentrations of DMSO were added to cells as controls.
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