CL-0124
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Product Introduction
| Cell Name | IMR-32 |
| Synonyms | IMR 32;IMR32;Institute for Medical Research-32;GM03320;GM3320C;GM03320D;AG03320;AG3320 |
| Cellosaurus Accession | CVCL_0346 |
| Organism | Human |
| Growth Properties | Adherent |
| Morphology | Fibroblast-like |
| Disease | neuroblastoma cells |
| Tissue | Brain; derived from metastatic site: abdominal mass |
| Age | 1Y1M |
| Sex | Male |
| Instructions | 1. Check all containers for leakage or breakage. 2. Remove the frozen cells from the dry ice packaging and immediately transfer them to liquid nitrogen (liquid or vapor phase) for long-term cryopreservation. |
| Complete Medium | MEM, with NEAA [PM150410]+10% Nutrient+1% Supplement |
| Incubation Atmosphere | Air, 95%; CO₂, 5% |
| Temperature | 37℃ |
| Subcultivation Ratio | 1:3-1:4 |
| Medium Renewal | 2 to 3 times per week |
| Dissociation Duration | 1-2 min |
| Subculturing Procedure | 1. Remove the culture medium from the T25 cell culture flask. 2. Add approximately 2 mL of PBS. Gently tilt the flask side to side until the PBS covers the entire bottom, then aspirate and discard the PBS. 3. Add 1 mL of 0.25% trypsin solution (containing EDTA). Gently tilt the flask side to side until the trypsin solution covers the entire bottom of the flask. 4. Incubate the cells at 37°C. Observe the cells under an inverted microscope and terminate digestion once the cells round up and detach. To avoid clumping, do not agitate the cells by tapping or shaking the flask during detachment. 5. Add 3 mL of complete culture medium to terminate digestion and disperse into a single cell suspension. 6. Collect the cell suspension and centrifuge at 1200 rpm (approximately 250 ×g) for 3 minutes. Carefully aspirate and discard the supernatant. 7. Add fresh complete culture medium, pipette gently several times to resuspend the cells, and seed them at the appropriate ratio into a new culture flask. Loosen the cap or use a vented cap for incubation. |
| Freeze Medium | General Freezing Medium [PB180436] |
| Storage Conditions | For long-term cryopreservation, cryovials should be stored in liquid nitrogen at −150°C to −196°C. Storage at −80°C is restricted to short-term interim use only. |
| Background | The IMR-32 cell line was established in April 1967 by W.W. Nichols, J. Lee, and S. Dwight from an abdominal mass obtained from a 13-month-old male infant. The pathological diagnosis was neuroblastoma with focal areas of organoid differentiation. IMR-32 cells comprise two morphologic populations: a predominant small neuroblast-like cell type and a large, hyaline, fibroblast-like cell type. The line was at passage 36 when submitted to the ATCC and has been shown to be subculturable beyond passage 80. |
| Biosafety Level | BSL-1 |
Documents
Publications
Journal: ACS Omega (2026) IF: 4.3
Product Cited: SK-N-AS Cells Line, SK-N-SH Cells Line, SK-N-BE(2) Cells Line, DMEM/F12 Medium, MEM Medium, Fetal Bovine Serum, SH-SY5Y Cells Line, DMEM (High glucose) Medium, IMR-32 Cells Line
Journal: ANTI-CANCER DRUGS (2026) IF: 2.2
DOI: 10.1097/CAD.0000000000001809
Product Cited: SK-N-SH Cells Line, MEM Medium, IMR-32 Cells Line, Human Astrocytes, Human Umbilical Vein Endothelial Cells, Human Astrocyte Complete Medium
Journal: JOURNAL OF MEDICINAL CHEMISTRY (2025) IF: 6.8
DOI: 10.1021/acs.jmedchem.5c02837
Product Cited: IMR-32 Cell Complete Medium, IMR-32 Cells Line
Journal: Cancers (2025) IF: 4.4
Product Cited: SH-SY5Y Cells Line, SK-N-BE (2) Cells Line, IMR-32 Cells Line
Journal: BRAIN RESEARCH (2025) IF: 2.6
DOI: 10.1016/j.brainres.2025.150071
Product Cited: Fetal Bovine Serum, SK-N-SH Cells Line, SK-N-AS Cells Line, Penicillin-Streptomycin Solution, 100 ×, IMR-32 Cells Line, MEM, with NEAA Medium, SK-N-BE (2) Cells Line
