CL-0271
$ 420.00
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1×10^6Cells/Vial×2Vials
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Product Introduction
General information
| Cell Name | D283 Med |
| Synonyms | D283 MED;D283-MED;D-283 Med;D-283MED;D283MED;D283Med;D283-Med;D283;Med 283;H283 |
| Cellosaurus Accession | CVCL_1155 |
| Organism | Human |
| Growth Properties | Semi-adherent and semi-suspension |
| Morphology | Epithelial-like |
| Tissue | Cerebellum; derived from metastatic site: ascites |
| Age | 6Y |
| Sex | Male |
Handling information
| 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. 3. This cell line proliferates slowly and has a long recovery period after cryopreservation. Medium changes should be performed every 4 days. If predominantly adherent growth is desired during culture, follow this recovery protocol: When adherent density is below 60%, collect floating cells during medium changes and return them to the original flask. When adherent density exceeds 60%, floating cells may be discarded during medium changes. Subculture when adherent density reaches 80%. |
| Complete Medium | MEM, with NEAA [PM150410]+10% Nutrient+1% Supplement |
| Incubation Atmosphere | Air, 95%; CO₂, 5% |
| Temperature | 37℃ |
| Subcultivation Ratio | 1:2-1:4 |
| Medium Renewal | 2 to 3 times per week |
| Dissociation Duration | 3-4 min |
| Subculturing Procedure | 1. This cell line displays mixed adherent and suspended phenotypes. Although suspended cells remain viable, their density is low and they may be aspirated and discarded directly. 2. Rinse the adherent cells with PBS, then add 1–2 mL of 0.25% Trypsin-EDTA to the culture flask. Incubate at 37°C. Once the cells round up and detach from the vessel surface, add 4–6 mL of complete medium to terminate digestion. Gently pipette to generate a single-cell suspension, then harvest cells by centrifugation. 3. Seed the cells into fresh culture vessels at the recommended split ratio. |
| Freeze Medium | Freezing Medium (Serum-free & animal origin-free) [PB180438] |
| 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. |
Reference materials
| Background | The D283 Med cell line was established in 1985 by Friedman et al. from the ascitic fluid of a 6-year-old Caucasian male with medulloblastoma and peritoneal metastasis. |
| Tumorigenic | Yes, in nude mice(The cells form serially transplantable intercranial and subcutaneous tumors.) Yes, in soft agar. |
| Gene Expression | The cells produce tumors in nude mice and the resulting tumors are glutamine synthetase positive; neuron specific enolase positive; glial fibrillary acidic proteins negative; S100 (S-100) protein negative; The cells express elevated levels of four biochemical markers of SCLC (neuron specific enolase; the brain isoenzyme of creatine kinase; L-DOPA decarboxylase; bombesin-like immunoreactivity) |
| Biosafety Level | BSL-1 |
Documents
Publications
Systematic decoding the functional role of human endogenous retrovirus-derived RNAs in medulloblastoma
Journal: Neuro-Oncology Advances (2026) IF: 4.1
Product Cited: MEM, with NEAA, D283 Med Cells Line
Circ-SKA3 upregulates ID3 expression by decoying miR-326 to accelerate the development of medulloblastoma
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
