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5 protocols using igr39

1

Culturing Human Cancer Cell Lines

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Human malignant melanoma cell line (IGR39), human colon adenocarcinoma cell line (HT-29), and human clear cell renal cell carcinoma line (CaKi-1) were obtained from American Type Culture Collection (ATCC, Manassas, VA). Cancer cell lines were cultured in DMEM Glutamax medium supplemented with 10% FBS and 1% antibiotics at 37 °C with 5% CO2 in a humidified atmosphere. Cell cultures were grown to 70% confluence, trypsinized with 0.125% TrypLE™ Express solution before passage, and used until passage 20.
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Culturing Human Cancer Cell Lines

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Human melanoma cancer cell line IGR39, human triple-negative breast cancer cell line MDA-MB-231, and human glioblastoma U-87 cell lines were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA). Cells were grown in DMEM Glutamax medium (Gibco, Carlsbad, CA, USA) containing 10% fetal bovine serum and 1% antibiotic mixture (10,000 U/mL penicillin and 10 mg/mL streptomycin; Gibco). All cells were incubated at 37 °C in a humidified atmosphere containing 5% CO2.
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Cell Culture Protocol for Cancer Cell Lines

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The human malignant melanoma cell line IGR39, human triple-negative breast cancer MDA-MB-231, and human pancreatic carcinoma cell line Panc-1 were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA). Human foreskin fibroblasts (HF) CRL-4001 were originally obtained from ATCC and kindly provided by Prof. Helder Santos (University of Helsinki, Finland). IGR39, MDA-MB-231, Panc-1, and HF were cultured in Dulbecco’s Modified Eagle’s GlutaMAX medium (Gibco (Carlsbad, CA, USA)). The medium was supplemented with 10,000 U/mL penicillin, 10 mg/mL streptomycin (Gibco), and 10% fetal bovine serum (Gibco). Cell cultures were grown at 37°C in a humidified atmosphere containing 5% CO2. They were used until the passage of 20.
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4

Culturing common cancer cell lines

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Human colon adenocarcinoma cell line (HT-29), human malignant melanoma cell line (IGR39), human clear renal carcinoma cell line (CaKi-1), and human endothelial cells (EC) CRL-1730 were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA). The cell culture medium consisted of DMEM Glutamax medium supplemented with 10% FBS and 1% antibiotics. Cells were kept at 37 °C with 5% CO2 in a humidified atmosphere and were grown to 70% confluence. During the passage, cells were trypsinized with 0.125% TrypLE™ Express solution and used till passage 20.
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5

Cell Culture of Cancer and Fibroblast Lines

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The human malignant melanoma cell line IGR39, human triple-negative breast cancer MDA-MB-231, and human pancreatic carcinoma cell line Panc-1 were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA). Human foreskin fibroblasts (HF) CRL-4001 were originally obtained from ATCC and kindly provided by Prof. Helder Santos (University of Helsinki, Finland). Primary prostate carcinoma PPC-1 cell line was kindly provided by Prof. Tambet Teesalu (University of Tartu, Estonia). All cell lines were cultured in Dulbecco’s Modified Eagle’s GlutaMAX medium (Gibco (Carlsbad, CA, USA)), supplemented with 10,000 U/mL penicillin, 10 mg/mL streptomycin (Gibco), and 10% fetal bovine serum (Gibco). Cell cultures were grown at 37 °C in a humidified atmosphere containing 5% CO2. They were used until the passage of 20.
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