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Found 4 matching solutions for this experiment
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MDCK II cells were maintained in Earle’s minimum essential medium supplemented with 4 mM glutamine, 0.2 mg/mL of both penicillin and streptomycin (Biochrom, Berlin, Germany), 10% (v/v) fetal calf serum (PAA, Pasching, Austria) in a 5% CO2 humidified incubator (HERA cell 150, Heraeus, Germany). Cells were subcultured weekly after reaching confluence by washing with PBS, followed by trypsinization and centrifugation at 110g. |
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MDCK II cells were maintained in Earle’s minimum essential medium supplemented with 4 mM glutamine, 0.2 mg/mL of both penicillin and streptomycin (Biochrom, Berlin, Germany), 10% (v/v) fetal calf serum (PAA, Pasching, Austria) in a 5% CO2 humidified incubator (HERA cell 150, Heraeus, Germany). Cells were subcultured weekly after reaching confluence by washing with PBS, followed by trypsinization and centrifugation at 110g. |
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Cells were propagated in Dulbecco's modified Eagle's medium (DMEM (Sigma D6429)), supplemented with 10% (v/v) heat‐inactivated foetal calf serum (FCS), penicillin (100 U/mL) and streptomycin (100 μg/mL) at 37°C with 5% (v/v) CO2. G418 sulphate (Geneticin; GIBCO) (1 mg/mL) was added to the culture medium for propagating MDCK‐SIAT1 cells. |
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Cells were propagated in Dulbecco's modified Eagle's medium (DMEM (Sigma D6429)), supplemented with 10% (v/v) heat‐inactivated foetal calf serum (FCS), penicillin (100 U/mL) and streptomycin (100 μg/mL) at 37°C with 5% (v/v) CO2. G418 sulphate (Geneticin; GIBCO) (1 mg/mL) was added to the culture medium for propagating MDCK‐SIAT1 cells. |
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enriched with fetal bovine serum at 1%, 25 µg/L of gentamicin, and 200 mmol/L of L-glutamine (maintenance medium) |
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enriched with fetal bovine serum at 1%, 25 µg/L of gentamicin, and 200 mmol/L of L-glutamine (maintenance medium) |
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supplemented with 10% fetal calf serum (FBS; Invitrogen) and 1% antibiotic/antimycotic (AA, GIBCO). |
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supplemented with 10% fetal calf serum (FBS; Invitrogen) and 1% antibiotic/antimycotic (AA, GIBCO). |
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