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2 protocols using snu 61

1

Culturing Human CRC Cell Lines

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Human CRC cell lines (colo-201, colo-205, colo-320, HCT-15, HCT-116, HT-29, Lovo, LS174T, SNU-61, SNU-70, SNU-81, SNU-175, SNU-254, SNU-283, SNU-407, SNU-977, SNU-1033, SNU-1181, SNU-1235, SNU-1411, SNU-1544, SNU-1684, SNU-C1, SNU-C2A, SNU-C4, SNU-C5, SW-403, and SW-480) were purchased from the Korean Cell Line Bank [18 (link)]. All cell lines were cultured in RPMI1640 (Hyclone Laboratories, Ind., Logan, UT), supplemented with 10% fetal bovine serum, at 37°C in humidified 5% CO2.
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2

Culturing and Differentiating Caco-2 and Human IECs

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The human epithelial cell line, Caco-2, was obtained from the ATCC. The cells were maintained in complete Dulbecco's modified Eagle medium (DMEM; Welgene, Daegu, Republic of Korea) with 10% fetal bovine serum (FBS; GIBCO, Burlington, ON, Canada) and 1% penicillin-streptomycin (Hyclone, Logan, UT, USA) at 37℃ in a humidified 5% CO 2 incubator. For differentiation/polarization, Caco-2 cells were plated on 12-mm transwell inserts with a 0.4μm pore polycarbonate membrane (Costar, Corning, NY, USA) and incubated for up to 21 days. The differentiation/ polarization was confirmed by measuring the trans-epithelial electrical resistance (TEER) at > 400 Ω•cm 2 with an EVOM2 (World Precision Instruments, Sarasota, FL, USA). Primary human IECs, SNU-61 and SNU-407 cells, were obtained from the Korean Cell Line Bank (Seoul, Republic of Korea) and cultured in complete Roswell Park Memorial Institute-1640 medium (Welgene) containing 10% FBS and 1% penicillin-streptomycin at 37℃ in a humidified CO 2 incubator.
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