CL-0615
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Product Introduction
| Cell Name | Daoy |
| Synonyms | DAOY;D324 Med;D-324 Med;D324 MED;D-324MED;D324 |
| Cellosaurus Accession | CVCL_1167 |
| Organism | Human |
| Growth Properties | Adherent |
| Morphology | Polygonal |
| Disease | neuroblastoma cells |
| Tissue | Brain |
| Age | 4Y |
| 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 | 1:3-1:6 |
| Medium Renewal | 2 to 3 times per week |
| Dissociation Duration | 2-3 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 Daoy cell line was established in 1985 by P. F Jacobsen of the Royal Perth Hospital in Western Australia. The line was derived from biopsy material taken from a tumor in the posterior fossa of a 4 year old boy. |
| Tumorigenic | Yes, in nude mice (The cells form serially transplantable intercranial and subcutaneous tumors.) |
| Biosafety Level | BSL-1 |
Documents
Publications
Journal: Biomaterials Research (2025) IF: 9.6
DOI: 10.34133/bmr.0237
Product Cited: D341Med Cells Line, Daoy Cells Line
Journal: MOLECULAR CARCINOGENESIS (2025) IF: 3.2
DOI: 10.1002/mc.70016
Product Cited: HT-1080 Cells Line, ES-2 Cells Line, Daoy Cells Line, MDA-MB-231 Cells Line, PC-3M Cells Line, Ramos Cells Line
Journal: MEDICAL ONCOLOGY (2023) IF: 3.4
DOI: 10.1007/s12032-023-01947-5
Product Cited: Daoy Cells Line
Journal: Journal Of Clinical Neuroscience (2021) IF: 2
DOI: 10.1016/j.jocn.2021.01.020
Product Cited: Daoy Cells Line, D283 Med Cells Line
