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Mem 10 010 cv

Manufactured by Corning
Sourced in United States

MEM (10-010-CV) is a cell culture medium designed to support the growth and maintenance of a variety of mammalian cell types. It provides the necessary nutrients, vitamins, and other components required for cell proliferation and survival. The medium is formulated to maintain a stable pH and osmotic balance, creating an optimal environment for cell culture applications.

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6 protocols using mem 10 010 cv

1

RCC Cell Lines Incubation and Treatments

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The human RCC cell lines (OS-RC-2, Caki-2, Caki-1, A498, 786-O, ACHN, 760-P, KETR-3) were obtained from the Chinese Academy of Sciences (Shanghai, China). A498 and ACHN cells were incubated in MEM(10-010-CV, Corning, United States) supplemented with 10% foetal bovine serum (FBS, 16000044, Gibco, United States) and other cells were incubated in RPMI-1640 (10-040-CV, Corning, United States) containing 10% FBS. Cells were grown as a monolayer on plastic cell culture dishes at 37 °C in a humidified atmosphere containing 5% CO2. Sorafenib and RITA (NSC 652287) were purchased from Selleck chemicals (China). MG132 and cycloheximide (CHX) was purchased from APExBIO (United States). The primers used were listed in Supplementary Table 8 and the antibodies used were listed in Supplementary Table 9.
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2

Cell Culture Protocols for Viral Studies

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Human astroglial SVG-A derived cells (a kind gift from Walter J. Atwood, Brown University, Providence, RI) were grown at 37 °C and 5% CO2 in Minimum Essential Medium (MEM) (10-010-CV; Corning) supplemented with 10% heat-inactivated fetal bovine serum (FBS, S11150; Atlanta Biologicals), penicillin, and streptomycin (1406-05-9; VWR International). African Green Monkey kidney epithelial MA104 cells (a kind gift from Siyuan Ding, Washington University in St. Louis, St. Louis, MO) were grown at 37 °C and 5% CO2 in Medium 199 supplemented with 10% heat-inactivated FBS. Vero C1008 (Vero 76, clone E6, Vero E6) [American Type Culture Collection (ATCC) CRL-1586] cells were cultured in Dulbecco’s Modified Eagle Medium (DMEM) supplemented with 10% FBS, and penicillin and streptomycin. Vero CCL-81 (ATCC CCL-81) cells were maintained in DMEM supplemented with 10% FBS, 10 mM Hepes pH 7.4, 1% Glutamax, and penicillin/streptomycin.
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3

Hypoxic Conditions for Renal Cancer Cell Lines

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The human RCC cell lines (Caki-2, A498, 786-O, ACHN) were obtained from the Chinese Academy of Sciences (Shanghai, China). A498 and ACHN cells were incubated in MEM (10-010-CV, Corning, USA) supplemented with 10% fetal bovine serum (FBS, 16000044, Gibco, USA) and other cells were incubated in RPMI-1640 (10-040-CV, Corning, USA) containing 10% FBS. Cells were grown as a monolayer on plastic cell culture dishes at 37 °C in a humidified atmosphere containing 5% CO2. All experimental cells were cultured under hypoxic conditions unless otherwise specified. Hypoxic conditions were achieved by culturing cells in a sealed chamber after flushing with 1% O2/5% CO2/94% N2, and the cells were cultured in hypoxic conditions for 12 or 24 h to model the hypoxic microenvironment. AMD3100 was purchased from Selleck chemicals (China), 2-Methoxyestradiol was purchased from APExBIO (USA), CXCL12 was purchased from R&D Systems (USA).
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4

Human Corneal Epithelial Cell Culture

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Human corneal epithelial (HCE) cells were provided by Deepak Shukla (University of Illinois at Chicago, Chicago, IL, USA). HCE cells were cultured in a Medium Essential Media (MEM) (10-010-CV, Corning, Cellgro, Manassas, VA, USA) supplemented with 10% Fetal Bovine Serum [(FBS), 26140-079, Gibco Life Technologies, Grand Island, NY, USA] and 1% penicillin- as reported prior [33 (link),34 ]. Standard cell culture conditions (37 °C, 5% CO2, > 95% humidity) were used during routine passages, as has been done previously [35 (link)]. HeLa cells were maintained in Dulbecco’s modified Eagle’s medium (DMEM; Life Technologies, Grand Island, NY, USA), and media were supplemented with 10% fetal bovine serum (FBS; Gibco/Life Technologies, Carlsbad, CA, USA) and 1% penicillin-streptomycin (Gibco/Life Technologies, Carlsbad, CA, USA).
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5

CFTR Variant Expression in CFBE Cells

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CFBE cell lines expressing CFTR variants (WT and R334W) with and without co-expression of the HS-YFP were cultured in minimum essential medium (MEM, #10-010-CV, Corning, VA, USA) supplemented with 10% fetal bovine serum (FBS, #LTI 10270-106, Gibco, Carlsbad, CA, USA) and 2 µg.mL-1 puromycin (#P8833, Sigma-Aldrich, St. Louis, MO, USA) [40 (link),41 (link)]. All cells were maintained at 37 °C and 5% CO2 in a humidified incubator, except for the low-temperature experiments, in which cells were cultured at 27 °C for 24 h.
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6

Renal Cell Carcinoma Cell Lines and Endothelial Cell Cultures

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Human RCC cell lines, including OS-RC-2 (cat. no. TCHu40), A498 (cat. no. HTB-44), 786-O (cat. no. TCHu186), ACHN (cat. no. TCHu199), KETR-3 (cat. no. CRL-1161) and human umbilical vein endothelial cells (HUVECs, cat. no. CRL-1730) were obtained from the Chinese Academy of Sciences (Shanghai, China) or the American Type Culture Collection (ATCC). The A498 and ACHN cells were cultured in MEM (10-010-CV, Corning, Inc.) supplemented with 10% fetal bovine serum (FBS, 16000044, Gibco; Thermo Fisher Scientific, Inc.), and the other RCC cells were cultured in RPMI-1640 (10-040-CV, Corning, Inc.) supplemented with 10% FBS. HUVECs were cultured in DMEM (Corning, Inc.) containing 10% FBS. The cells were grown in a single layer on a plastic cell culture dish in humidified air containing 5% CO2 at 37°C. Sunitinib was purchased from Shanghai Selleck Chemicals Co., Ltd. MG132 and cycloheximide (CHX) were obtained from Apexbio Technology, LLC. Recombinant human glutamine peptide loop transferase/QPCT (6368-Zn) was obtained from R&D Systems. Matrigel matrix basement membrane matrix (354234, BD Biosciences) was purchased from Corning, Inc.
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