SH-SY5Y neuroblastoma cell line were purchased from ATCC (ATCC® CRL-2266™). The cells were initially grown in Dulbecco’s Modified Essential Medium (DMEM:F12) which contains 4.5 g/l glucose with 2mM of L-glutamine and sodium pyruvate, supplemented with 15% FBS, 1% of Penicillin-Streptomycin mixed solution and 1% NEAA at 37°C with 5% carbon dioxide (CO2). Then, the cells were induced with 10 μM of all-trans retinoic acid for 5 days in a differentiation media (DMEM:F12, supplemented with 2.5% Fetal bovine serum (FBS) and 1% of Penicillin-Streptomycin mixed solution) (Forster et al., 2016 (link); Izham et al., 2018 (link)).
SH-SY5Y Neuroblastoma Cell Differentiation
SH-SY5Y neuroblastoma cell line were purchased from ATCC (ATCC® CRL-2266™). The cells were initially grown in Dulbecco’s Modified Essential Medium (DMEM:F12) which contains 4.5 g/l glucose with 2mM of L-glutamine and sodium pyruvate, supplemented with 15% FBS, 1% of Penicillin-Streptomycin mixed solution and 1% NEAA at 37°C with 5% carbon dioxide (CO2). Then, the cells were induced with 10 μM of all-trans retinoic acid for 5 days in a differentiation media (DMEM:F12, supplemented with 2.5% Fetal bovine serum (FBS) and 1% of Penicillin-Streptomycin mixed solution) (Forster et al., 2016 (link); Izham et al., 2018 (link)).
Corresponding Organization : Australian Research Council
Other organizations : National University of Malaysia
Variable analysis
- Lipopolysaccharide (LPS) from Escherichia coli O55:B5
- SH-SY5Y neuroblastoma cell line response (not explicitly specified)
- DMEM:F12 culture medium
- Fetal bovine serum (FBS)
- Penicillin-Streptomycin solution
- Non-essential amino acids (NEAA)
- Incubation conditions (37°C, 5% CO2)
- Untreated SH-SY5Y neuroblastoma cells
- None specified
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