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2 protocols using mia paca 2

1

Culture of Pancreatic Cancer Cell Lines

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EGFR-positive human pancreatic cancer cell lines AsPC-1, BxPC-3 and MIA PaCa-2 were obtained from American Type Culture Collection. AsPC-1 and BxPC-3 cells were cultured in modified RPMI medium (HyClone; GE Healthcare Life Sciences) supplemented with 10% fetal bovine serum (FBS), 100 U/ml penicillin and 100 µg/ml streptomycin (Gibco; Thermo Fisher Scientific, Inc.). MIA PaCa-2 cells were cultured in high glucose DMEM (HyClone; GE Healthcare Life Sciences) supplemented with the same additives. The cells were cultured in a humidified incubator (Thermo Fisher Scientific, Inc.) at 37°C with 95% air and 5% CO2.
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2

Culturing Pancreatic Cancer Cell Lines

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Human PDAC cell lines (MIA PaCa-2, PANC-1, HPAF-II, AsPC-1, and Bx PC-3) were obtained from American Type Culture Collection, Manassas, VA, USA. hTERT-HPNE cells were obtained from Dr. Channing Der’s laboratory at UNC, Chapel Hill, NC. MIA PaCa-2 cells were cultured in DMEM (Dulbecco’s Modified Eagle Medium) high-glucose media (GE Healthcare Life Sciences, Chicago, IL, USA) containing 10% (v/v) fetal bovine serum (Atlanta Biologicals, Flowery Branch, GA, USA) and 2.5% (v/v) horse serum (Corning, Corning, NY, USA). PANC-1 cells were cultured in DMEM high-glucose media containing 10% (v/v) FBS. HPAF-II cells were cultured in Eagle’s Minimum Essential Medium (EMEM) (Corning, Corning, NY, USA) containing 10% v/v fetal bovine serum (FBS). AsPC-1 were cultured in RPMI-1640 (GE Healthcare Life Sciences) containing 10% FBS (v/v). Cells were maintained at 37 °C with 5% CO2. The cell lines were subcultured by enzymatic digestion with 0.25% trypsin/1 mM EDTA solution (GE Healthcare Life Sciences, Chicago, IL, USA) when they were 80% confluent. All cell lines tested negative for Mycoplasma contamination.
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