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3 protocols using rmi 1640

1

Culturing Human Liver Cell Lines

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The human HCC cell lines, HCC-LM3 and SMMC-7721, as well as the normal liver cell line LO2, were obtained from the Cell Bank of the Chinese Academy of Sciences (Shanghai, China). The cells were cultured in RMi-1640 (Gibco, NY) or DMEM (Gibco, NY) medium supplemented with 10% fetal bovine serum (FBS; Gibco, Grand Island, NY, USA) and 1% penicillin-streptomycin (P/S; Gibco, USA). The cell cultures were maintained in a humidified incubator (Thermo Scientific, Waltham, MA, USA) at 37°C with 5% CO2.
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2

Culturing Colorectal Cancer Cell Lines

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Human colorectal cancer cell lines HT-29, HCT-116, SW480, SW620, LoVo, SW48, DLD-1, Caco-1 and HCT-15 cells were maintained in RMI-1640 (Gibco, Thermo Fisher Scientific, Waltham, MA, USA), supplemented with 10% FBS, 200 mM Lglutamine, 1%PS, and placed in a wet incubator at 37°C and 5% CO2 (link). 5-FU (F6627-10G) was purchased from Sigma (Poole, UK), and soluble in dimethyl sulfoxide. Colorectal cancer cells were treated with 5-FU at 5 μg/mL.
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3

Evaluating RP11-789C1.1 in ATR-CHK1 Signaling

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Human GC cell lines (AGS, MKN-45, BGC-823, KATOIII, HGC-27, and SGC-7901) and normal gastric epithelial cells (GES-1) were obtained from Procell Life Science & Technology Co., Ltd., Wuhan, China and Zhong Qiao Xin Zhou Biotechnology Co., Ltd., Shanghai, China. All cell lines were verified by mycoplasma detection and short tandem repeat (STR) profiling. Cells were cultured in RMI-1640 supplemented with 10% fetal bovine serum (Gibco BRL, Grand Island, USA) and Dulbecco's Modified Eagle Medium (DMEM) (Gibco, Grand Island, USA) at 37°C in 5% CO2 atmosphere. To evaluate the effects of RP11-789C1.1 in ATR-CHK1 signaling pathway, the cells were treated with concentrations of AZD6738 (1 µmol/L, S7693, Sellleck, Texas, USA) for 12 hours.
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