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6 protocols using HDPSCs

Human dental pulp stem/stromal cells (hDPSCs) obtained from AllCells, LLC (Cat. DP0037F, Lot N° DPSC090411-01) were maintained in MEM α, GlutaMAX™ Supplement, no nucleosides (Gibco, 32561029), supplemented with 10% (v/v) fetal bovine serum (FBS) (Gibco, A3160802), 100 IU/mL penicillin, 0,1 mg/mL streptomycin (Gibco, 15140122), 2.05 µm/mL amphotericin B (Gibco, 15290026) and 10 mM HEPES buffer solution (Gibco, 15630122). All cells are maintained at 37 °C, 80% humidified atmosphere and 5% CO2 environment. Campos et al. previously described the characterization of these cellular populations [34 (link)].
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The human dental pulp stem/stromal cells (hDPSCs) used in this study were sourced from AllCells, LLC (Cat. DP0037F, Lot No. DPSC090411-01). These were maintained in MEM α, GlutaMAX™ supplement, nucleoside-free (Gibco, 32561029). This medium was supplemented with 10% (v/v) foetal bovine serum (FBS) (Gibco, A3160802), 100 IU/mL penicillin, 0.1 mg/mL streptomycin (Gibco, 15140122), 2.05 µm/mL amphotericin B (Gibco, 15290026) and 10 mM HEPES buffer solution (Gibco, 15630122). DPSCs were maintained in standard conditions, namely at 37 °C in 80% humidified atmosphere and 5% CO2.
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Human Dental Pulp stem/stromal cells (hDPSCs) obtained from AllCells, LLC, Alameda, CA, USA (Cat. DP0037F, Lot no. DPSC090411-01) were maintained in MEM α, GlutaMAX™ Supplement, no nucleosides (Gibco, 32561029), supplemented with 10% (v/v) fetal bovine serum (FBS) (Gibco, A3160802), 100 IU/mL penicillin, 0.1 mg/mL streptomycin (Gibco, 15140122), 2.05 µm/mL amphotericin B (Gibco, 15290026), and 10 mM HEPES buffer solution (Gibco, 15630122), Thermo Fisher Scientific, Waltham, MA USA. All the cells were maintained at 37 °C, 80% humidified atmosphere, and 5% CO2 environment. A characterization study of these cells is described by Campos et al. [25 (link)].
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hDPSCs were acquired from AllCells, LLC (Cat. DP0037F, Lot N° DPSC090411-01) and maintained in MEM α, GlutaMAX™ Supplement, no nucleosides (Gibco, 32561029), supplemented with 10% (v/v) fetal bovine serum (FBS) (Gibco, A3160802), 100 IU/mL penicillin, 0.1 mg/mL streptomycin (Gibco, 15140122), 2,05 µm/mL amphotericin B (Gibco, 15290026) and 10 mM HEPES buffer solution (Gibco, 15630122). Cells were maintained at 37 °C, 80% humidified atmosphere and 5% CO2 environment. A previous work details the characterization of these cells [37 (link)].
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hDPSCs were obtained from AllCells, LLC (Cat. DP0037F, Lot No. DPSC090411-01). Cells were thawed and expanded in vitro using standard protocols previously reported [17–29 (link)]. hPDSCs were maintained in αMEM, with GlutaMAX™, without nucleosides (32561029, Gibco®) supplemented with 10% (v/v) fetal bovine serum (A31608-02, Gibco®), 100 IU/ml penicillin, 0.1 mg/ml streptomycin (15140122, Gibco®), 2.05 µg/ml amphotericin B (15290026, Gibco®) and 10 mM 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid Buffer solution (15630122, Gibco®), kept at 37°C and in a 95% humidified atmosphere with 5% CO2.
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The hDPSCs (Allcells, Emeryville, CA, USA) were cultured in α-MEM containing 10% FBS and 1/100 volume of antibiotic liquid at 37°C and 5% CO 2. When the cells reached subconfluence, the cells were harvested using a 0.25% trypsin solution containing 0.02% EDTA and subcultured according to a conventional method. The hDPSCs subcultured 12-14 times were used in the experiment.
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