Human neuroblastoma cell lines IMR-32, SK-N-SH, and SH-SY5Y were obtained from the ATCC. IMR-32 and SK-N-SH cells were grown in ATTC Eagle’s Minimum Essential Medium (EMEM) supplemented with 10% FBS. SH-SY5Y cells were cultured in ATCC EMEM mixed 1:1 with F12 medium, and FBS was added to a final concentration of 10%.
Murine and Human Neuroblastoma Cell Culture
Human neuroblastoma cell lines IMR-32, SK-N-SH, and SH-SY5Y were obtained from the ATCC. IMR-32 and SK-N-SH cells were grown in ATTC Eagle’s Minimum Essential Medium (EMEM) supplemented with 10% FBS. SH-SY5Y cells were cultured in ATCC EMEM mixed 1:1 with F12 medium, and FBS was added to a final concentration of 10%.
Corresponding Organization : George Washington University
Variable analysis
- In vivo passaging of Neuro2a cells to derive the AgN2a subclone
- Characteristics of the Neuro2a and AgN2a cell lines
- Growth characteristics of human neuroblastoma cell lines IMR-32, SK-N-SH, and SH-SY5Y
- Growth medium composition for Neuro2a and AgN2a cells (DMEM, 1% penicillin-streptomycin, 10% fetal bovine serum)
- Growth medium composition for mouse splenocytes (RPMI, 2 mM L-glutamine, 10% fetal bovine serum, 1% penicillin-streptomycin)
- Growth medium composition for human neuroblastoma cell lines (EMEM, 10% FBS; EMEM mixed 1:1 with F12, 10% FBS)
- Incubation conditions (37°C, 5% CO2)
- None specified
- None specified
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