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2 protocols using h45 hypoxystation

1

Culturing Pancreatic Cancer Cell Lines

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PANC-1 [American Type Culture Collection (ATCC), CRL-1469], BxPC-3 (ATCC, CRL-1687), SK-PC-3, and GP-9A cells were cultured in RPMI 1640 (Sigma-Aldrich). Capan-2 (ATCC, HTB-80) cells were cultured in McCoy 5A (Sigma-Aldrich). MIA PaCa-2 (ATCC, CRL-11268), GP-2A, GP-3A, GP-5A, GP-9A, GP-10A, and GP-16A cells were cultured in Dulbecco’s modified Eagle’s medium (Sigma-Aldrich). All media were supplemented with 2 to 10% fetal bovine serum (Gibco) and cultured under conditions of 5% CO2 in air at 37°C. For primary pancreatic cancer cells, 1× penicillin/streptomycin was added in the growth medium. For hypoxia, cells were transferred to H45 Hypoxystation (Don Whitley Scientific). The DNA-PK inhibitor NU7441 (10 μM, Medchem Express) was added at the time of seeding and replenished 1 hour before collecting the cells.
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2

Pancreatic Cancer Cell Culture Conditions

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PANC-1 (ATCC, CRL-1469), BxPC-3 (ATCC, CRL-1687), SK-PC-3 and GP-9A cells were cultured in RPMI-1640 (Sigma). Capan-2 (ATCC, HTB-80) cells were cultured in McCoy 5A (Sigma). MIA PaCa-2 (ATCC, CRL-11268), GP-2A, GP-3A, GP-5A, GP-9A, GP-10A and GP-16A cells were cultured in DMEM (Sigma). All media was supplemented with 2%-10% fetal bovine serum (Gibco) and cultured under conditions of 5% CO2 in air at 37⁰C. For primary pancreatic cancer cells 1X penicillin/streptomycin was added in the growth media. For hypoxia, cells were transferred to a H45 Hypoxystation (Don Whitley Scientific). DNA-PK inhibitor Nu7441 (10 µM, Medchem Express) was added at the time of seeding and replenished one hour before collecting the cells.
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