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Found 3 matching solutions for this experiment
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NHDF were maintained in fibroblasts growth media 2 (FGM2, Promocell) under the physiological culture conditions (37°C, 5% CO2), and subcultured using DetachKit2-Promocell HEPES BSS (4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid buffered saline solution); 0.04% trypsin/0.03% Ethylenediaminetetraacetic acid (EDTA); trypsin neutralizing solution (TNS) containing 0.05% trypsin inhibitor from soybean/0.1% bovine serum albumin). |
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NHDF were maintained in fibroblasts growth media 2 (FGM2, Promocell) under the physiological culture conditions (37°C, 5% CO2), and subcultured using DetachKit2-Promocell HEPES BSS (4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid buffered saline solution); 0.04% trypsin/0.03% Ethylenediaminetetraacetic acid (EDTA); trypsin neutralizing solution (TNS) containing 0.05% trypsin inhibitor from soybean/0.1% bovine serum albumin). |
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Dermal fibroblasts were cultured in Dulbecco’s modified Eagle medium(DMEM; D6546, Sigma-Aldrich) supplemented with 10% foetal bovine serum (HyClone), 2 mM L-glutamine (G7513, Sigma-Aldrich)and 1% penicillin-streptomycin (P0781, Sigma-Aldrich) in a humidified incubator (37°C, 5% CO2). Cells were passaged once a week at a 1:4 split ratio |
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Dermal fibroblasts were cultured in Dulbecco’s modified Eagle medium(DMEM; D6546, Sigma-Aldrich) supplemented with 10% foetal bovine serum (HyClone), 2 mM L-glutamine (G7513, Sigma-Aldrich)and 1% penicillin-streptomycin (P0781, Sigma-Aldrich) in a humidified incubator (37°C, 5% CO2). Cells were passaged once a week at a 1:4 split ratio |
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supplemented with 10% SERA Plus specially processed fetal bovine serum (FBS) (PAN biotech GmbH), penicillin (100 U/mL), streptomycin (100 μg/mL), and L-glutamine (2 mM). |
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supplemented with 10% SERA Plus specially processed fetal bovine serum (FBS) (PAN biotech GmbH), penicillin (100 U/mL), streptomycin (100 μg/mL), and L-glutamine (2 mM). |
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