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Ham s f12 nutrient medium

Manufactured by Thermo Fisher Scientific
Sourced in United States

Ham's F12 nutrient medium is a cell culture medium designed to support the growth and maintenance of various cell types, including those derived from Chinese hamster ovary (CHO) cells. It is a complex medium that provides essential nutrients, vitamins, and other components required for cell proliferation and survival. The medium is formulated to maintain the appropriate pH, osmolarity, and ionic balance necessary for optimal cell growth and function.

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4 protocols using ham s f12 nutrient medium

1

Cultivation of Cell Lines for Cancer Research

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The ccRCC (786-0) cell line with CAIX antigen overexpressed was obtained from the Key Laboratory for Cancer Biology Treatment of Xuzhou Medical College as a gift. EA.hy926 normal human umbilical vein endothelial cell line (HUVEC) that is absent of CAIX antigen expression and human lung fibroblast HLF-1 cells were kindly provided by Teng Fei (Laboratory of Medical Imaging of Xuzhou Medical College). The original source of these three kinds of cell lines was from the same commercial source, the Cell Bank of the Chinese Academy of Sciences (Shanghai, China). NIH-3T3 mouse fibroblast cells were also purchased from it. The 786-0 renal carcinoma cells were cultured in a 10% FBS-containing RPMI 1640 medium (Gibco, Grand Island, NY) supplemented with penicillin (100 µg/mL), and streptomycin (100 µg/mL). NIH-3T3 and HUVEC cells were propagated in 10% FBS-containing DMEM medium (Gibco, Grand Island, NY) supplemented with penicillin (100 µg/mL), and streptomycin (100 µg/mL). HLF-1 cells were cultured in Ham’s F12 nutrient medium (Gibco, Grand Island, NY) supplemented with 10% FBS, penicillin (100 µg/mL), and streptomycin (100 µg/mL). All cells were grown in a humidified incubator (Thermo, USA) at 37°C under 5% CO2 atmosphere.
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2

Culturing Colorectal Cancer Cell Lines

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As described [8 (link),9 (link)], colorectal cancer cell lines, including HT-29, DLD-1 and Caco-2, were purchased from the cell bank of Chinese Academy of Science (CAS) Shanghai Biological Institute (Shanghai, China). Cells were maintained in FBS-containing RPMI/DMEM medium. Human NCM460 colon epithelial cell line was provided by Fudan IBS Cell center (Shanghai, China). Cells were cultured in Ham's F12 nutrient medium (Gibco) [19 (link)].
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3

CHO Cell Culture and Chemical Treatments

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Chinese hamster ovary cells (CHO–K1) (ATCC CRL-9618) were maintained in Ham’s F12 Nutrient medium (Gibco) supplemented with 10% heat-inactivated fetal bovine serum (FBS) (Gibco) at 37 °C in a humidified environment containing 5% CO2. Cells were subcultured every 3 days in 25- or 75-cm2 flasks. All chemicals were dissolved in absolute ethanol (Sigma, St. Louis, MO) and were then added at various concentrations to cells for 48 h. The final ethanol concentration was less than 0.1%.
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4

Neuroblastoma Cell Culture and Tissue Collection

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Human NB cell lines, CHLA15, CHLA136, SK-N-SH, SH-SY5Y, and SK-N-AS, were maintained in high glucose DMEM (Hyclone, Logan, UT, USA), while SK-N-BE(2)C and SK-N-BE(2) cells were maintained in Ham’s F 12 nutrient medium (Gibco, Gaithersburg, MD, USA). Among these cell lines, SK-N-BE(2) and SH-SY5Y was purchased from the Cell Bank of the Chinese Academy of Science (Shanghai, China) and other cells were kind gifts from Professor Kai Li of Children’s Hospital of Fudan University. Both media were supplemented with 10% fetal bovine serum (FBS; Gibco) and penicillin-streptomycin solution (Gibco), and cells were cultured at 37 °C in a humidified atmosphere containing 5% CO2. Our study collected primary NB tumor tissues and peritumoral tissues from the Children’s Hospital of Fudan University. All patients with NB were diagnosed by pathology department and did not receive any treatment prior to surgery. Informed consent was obtained from each patient or legal guardian. And the methods were performed in accordance with relevant guidelines and regulations and approved by Committee of Children’s hospital of Fudan University.
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