CL-0238
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Product Introduction
| Cell Name | U-87 MG |
| Synonyms | U-87MG;U-87 MG;U87 MG;U-87-MG;U87-MG;U87MG;U-87;U87;87 MG;87MG |
| Cellosaurus Accession | CVCL_0022 |
| Organism | Human |
| Growth Properties | Adherent |
| Morphology | Epithelial-like |
| Disease | glioma cells |
| Tissue | Brain |
| Age | Age unspecified |
| 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. 3. This cell line is prone to cell aggregation. This can be improved by coating culture vessels with Poly-L-Lysine solution or gelatin. It is recommended to prepare Poly-L-Lysine solution (Cat. No.:PB180523). |
| 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 | 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 | 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. |
| Background | The U-87 MG cell line was established by Pontén J et al. and derived from a malignant glioma. U-87 MG cells are tumorigenic when inoculated subcutaneously into nude mice. |
| Tumorigenic | Yes, in nude mice inoculated subcutaneously with 1×10⁷ cells. |
| Biosafety Level | BSL-1 |
Documents
Publications
Journal: Biochemistry and Cell Biology (2023) IF: 2.9
Product Cited: U-87 MG Cells Line, U251 Cells Line, SHG-44 Cells Line, U373 Cells Line
Journal: Oncology Letters (2023) IF: 2.9
Product Cited: U-87 MG Cells Line, LN229 [LN-229; LNT-229] Cells Line, U251 Cells Line
Journal: FUNCTIONAL & INTEGRATIVE GENOMICS (2023) IF: 2.9
DOI: 10.1007/s10142-023-01217-7
Product Cited: U-87 MG Cells Line, U251 Cells Line
Journal: TECHNOLOGY IN CANCER RESEARCH & TREATMENT (2023) IF: 2.8
DOI: 10.1177/15330338231218218
Product Cited: HA1800 Cells Line, T98G Cells Line, U-87 MG Cells Line
Journal: PeerJ (2023) IF: 2.7
DOI: 10.7717/peerj.16104
Product Cited: U-87 MG Cells Line, U251 Cells Line
