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The EC9706 is a laboratory centrifuge designed for a wide range of applications in cell culture, molecular biology, and biochemistry. It features a compact and robust construction, accommodating various rotor configurations to enable efficient separation of cells, organelles, and other biomolecules.

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47 protocols using ec9706

1

Esophageal Cancer Cell Line Transfection

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The human esophageal epithelial cell line (Het-1a) and the EC cell lines EC9706, Eca109, EC1, KYSE30 cells were purchased from the Type Culture Collection of the Chinese Academy of Sciences. Esophageal cancer cell lines were maintained in RPMI 1640 medium with 10% fetal bovine serum (FBS; Gibco) and were incubated at 37 °5% CO2. Het-1a cell line was maintained in Dulbecco’s Modified Eagle medium with high glucose. The small interfering RNA, microRNA (miRNA) mimics, and inhibitors were purchased from Shanghai Genepharma Co, Ltd and were transfected into cells with the BTX ECM 2001 square wave electroporator according to the BTX Molecular Delivery Systems protocol.
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2

Culturing Esophageal and EC Cell Lines

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The human esophageal cell line, HET-1A, and EC cell lines Eca109, EC-1, EC9706, KYSE30 and KYSE150 were purchased from the Type Culture Collection of the Chinese Academy of Sciences (Shanghai, China). The cell lines were cultured in RPMI-1640 medium supplemented with 10% fetal bovine serum (FBS, Gibco, Australia), 100 U/mL penicillin, and 50 μg/mL streptomycin, and were kept in incubators with humidified atmospheres of 5% CO2 and 95% air at 37°C.
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3

Esophageal Squamous Cell Carcinoma Cell Lines

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Six human ESCC cell lines (EC9706, EC109, KYSE150, KYSE450, TE1, and TE10) were obtained from the Type Culture Collection of the Chinese Academy of Sciences (Shanghai, China). The human esophageal epithelial cell line (HET1A) was obtained from the American Type Culture Collection (ATCC). EC9706, EC109, KYSE150, KYSE450, TE1, and TE10 cells were cultured in RPMI-1640 medium (HyClone; GE Healthcare) containing 10% fetal bovine serum (FSB; HyClone; GE Healthcare) and 1% penicillin/streptomycin (Sigma-Aldrich; Merck KGaA). The HET1A cells were cultured in Dulbecco's modified Eagle's medium (DMEM; HyClone; GE Healthcare) supplemented with 10% FBS and 1% penicillin/streptomycin. All cells were grown in a humidified atmosphere with 5% CO2 at 37°C.
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4

ESCC Cell Line Culturing Protocol

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The three human ESCC cell lines (KYSE150, ECA-109 and EC9706) and normal epithelial cell line (HET-1A) were purchased from the Type Culture Collection of the Chinese Academy of Sciences (Shanghai, China). All cell lines were maintained in RPMI-1640 medium (Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA) supplemented with 10% fetal bovine serum (FBS; Gibco; Thermo Fisher Scientific, Inc.) at 37°C in a humidified chamber with 5% CO2.
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5

Culture of Human Esophageal Cancer Cells

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The EC9706 human esophageal squamous cell carcinoma cell line was obtained from the Type Culture Collection of the Chinese Academy of Sciences (Beijing, China). The cells were cultured in RPMI-1640 medium supplemented with 10% fetal bovine serum, 2 mM glutamine, 100 units/ml penicillin and 100 µg streptomycin/ml (all purchased from Sigma-Aldrich, St. Louis, MO, USA). The cells were incubated at 37°C in a humidified atmosphere containing 95% air and 5% CO2, and were sub-cultured every three days.
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6

Esophageal Cancer Cell Line Culturing

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Human ESCC cell lines (KYSE30, KYSE150, TE-1, EC109, and EC9706) and immortalized esophageal epithelial cell line (HET-1A) was purchased from Type Culture Collection of the Chinese Academy of Sciences (Shanghai, China). KYSE30 and KYSE150 were cultured in RPMI 1640 medium (GIBCO) supplemented with 10% fetal bovine serum (FBS). TE-1, EC109, and EC9706 cell lines were cultured in DMEM (GIBCO) supplemented with 10% FBS. HLECs were purchased from ScienCell Research Laboratories and cultured in ECM complete medium (ScienCell Research Laboratories). For exosomes co-culture, 1 μg/mL (as determined by BCA protein assay (Thermo Fisher Scientific, USA) of exosomes were added to the culture medium of recipient cells (5 × 106).
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7

Culturing ESCC Cell Lines

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Cell line and materials. EC109 and EC9706 cells (Type Culture Collection of the Chinese Academy of Sciences, Shanghai, China), which are well and poorly differentiated human ESCC cell lines, respectively, were cultured in Dulbecco's modified Eagle's medium (DMEM; Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA)
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8

Esophageal Carcinoma Cell Lines and Xenograft Model

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Human ESCC cell lines EC9706, ECa109, and EC1 were obtained from Type Culture Collection of the Chinese Academy of Sciences (Shanghai, China). Cells were cultured in RPMI/1640 medium with 10% FBS, 100 U/mL penicillin, and 100 μg/mL streptomycin at 37°C in a humidified atmosphere consisting of 5% CO2, as described in our previous study [19 (link)]. Male athymic BALB/c nude mice (Slack King of Experimental Animals Co. Ltd., Wuhan, China) at 4 to 6 weeks of age and 18 to 22 g of weight were used in this study. All the animals were housed in independently ventilated cages (IVC) at a temperature of 25-26°C and a relative humidity of ~50%, lit 12 hours/day. All animal studies were carried out in compliance with the Guide for the Care and Use of Laboratory Animals of Henan Province, China. The data of patient tissue samples were described as in our previous paper [20 (link)].
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9

Cultivation of Esophageal Cancer Cell Lines

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Human esophageal carcinoma cell lines EC109 and EC9706 were purchased from the Type Culture Collection of the Chinese Academy of Sciences (Shanghai, China), which were cultured in Dulbecco's modified Eagle's medium (DMEM) with 10% fetal bovine serum at 37°C and 5% CO2. All experiments were carried out when the cells reached 60% confluency.
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10

Cell Line Maintenance Protocol

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EC1, EC9706, and HET‐1A cells were purchased from the Type Culture Collection of the Chinese Academy of Sciences (Shanghai, China). All cells were maintained in RPMI 1640 medium supplemented with 10% foetal bovine serum (FBS; Gibco BRL, Gaithersburg, MD, USA) and incubated at 37°C and 5% CO2.
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