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The Ca-Ski is a laboratory equipment designed for the measurement of intracellular calcium concentration. It utilizes fluorescent dyes to detect and quantify the levels of calcium ions within cells. The core function of the Ca-Ski is to provide researchers with accurate and reliable data on calcium homeostasis in various biological systems.

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3 protocols using ca ski

1

Cervical Cancer Tissue Acquisition and Cell Line Culture

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This study was approved by the Ethics Committee of Tianjin Hospital. Written informed consent was also obtained from each patient who participated in this research. A total of 45 paired cervical cancer tissues and corresponding adjacent normal tissues were obtained from cervical cancer patients who had undergone surgery between October 2014 and August 2016 in the Department of Obstetrics and Gynecology, Tianjin Hospital. None of the patients received chemotherapy, radiotherapy, or other treatments before surgery. Tissues were immediately frozen in liquid nitrogen and stored at −80°C until further use.
Four human cervical cancer cell lines (HeLa, SiHa, Ca-Ski, and C-33A) were purchased from the Shanghai Institute of Biochemistry and Cell Biology (Shanghai, P.R. China). Ect1/E6E7, a human normal cervical epithelial cell line, was acquired from the American Type Culture Collection (ATCC; Manassas, VA, USA). All cell lines were cultured in Dulbecco’s modified Eagle’s medium (DMEM) containing 10% fetal bovine serum (FBS), 100 U/ml penicillin, and 100 mg/ml streptomycin (all from Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA). All cell lines were grown in a humidified atmosphere at 37°C with 5% CO2.
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2

Cultured Human Cervical Cell Lines

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A normal human cervix epithelial cell line (Ect1/E6E7) was acquired from the American Type Culture Collection (Manassas, VA, USA). Four human cervical cancer cell lines (HeLa, C-33A, SiHa, and CaSki) were ordered from the Shanghai Institute of Biochemistry and Cell Biology (Shanghai, China). Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% (v/v) of heat-inactivated fetal bovine serum (FBS) and 1% (v/v) of a penicillin/streptomycin solution (all from Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA) was used to culture all the above cell lines. All cells were grown at 37°C in a humidified incubator supplied with 5% CO2.
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3

Cervical Cancer Cell Line Treatments

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Human cervical squamous cell carcinoma cell lines (Ca-Ski, Hela, SiHa and c-33A) were obtained from Shanghai Institute of Biochemistry and Cell Biology (Shanghai, China). A non-cancerous ectocervical epithelial cell line (Ect1/E6E7) was obtained from American Type Culture Collection (ATCC) and maintained in Gibco® Keratinocyte-Serum Free medium with 0.1 ng/ml human recombinant epidermal growth factor, 0.05 mg/ml bovine pituitary extract, and 0.4 mM calcium chloride. Ca-Ski cells were cultured in the Gibco® RPMI-1640 medium and the other cells were cultured in the Gibco® DMEM medium (Thermo Fisher Scientific, Inc.) supplemented with 10% Gibco FBS (Thermo Fisher Scientific, Inc.) and 1% penicillin-streptomycin. All cell lines were incubated at 37˚C in an incubator in an atmosphere containing 5% CO2. The cells were treated with 30 µM Tat-BECN1 (Selleck Chemicals), a potent and specific autophagy inducer via activating Beclin1 (19 ,20 (link)), or 200 ng/ml TNF-related apoptosis-inducing ligand (TRAIL; Merck KGaA).
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