CL-0087
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Product Introduction
| Cell Name | H4 |
| Synonyms | H-4 |
| Cellosaurus Accession | CVCL_1239 |
| Organism | Human |
| Growth Properties | Adherent |
| Morphology | Epithelial-like |
| Disease | glioma cells |
| Tissue | Brain |
| Age | 37Y |
| 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 | DMEM [PM150210]+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 | 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 H4 cell line was established in 1973. It was derived from brain tissue of a 37-year-old patient with glioma. The tumorigenic properties of H4 cells are suppressed; generally, no tumor nodules form when the cells are inoculated into animals. H4 cells possess the ability to repair MNNG-damaged adenovirus type 5. |
| Tumorigenic | No, in immunosuppressed mice. Yes, in semisolid medium. |
| Biosafety Level | BSL-1 |
Documents
Publications
Journal: Cell Death Discovery (2024) IF: 6.1
DOI: 10.1038/s41420-024-02105-0
Product Cited: LN229 [LN-229; LNT-229] Cells Line, H4 Cells Line, HA1800 Cells Line, A172 Cells Line, U-87 MG Cells Line
Journal: CELLULAR SIGNALLING (2024) IF: 4.4
DOI: 10.1016/j.cellsig.2024.111137
Product Cited: U-87 MG Cells Line, LN229 [LN-229; LNT-229] Cells Line, H4 Cells Line, A172 Cells Line
Journal: PHARMACOLOGICAL RESEARCH (2023) IF: 9.3
DOI: 10.1016/j.phrs.2023.106979
Product Cited: U251 Cells Line, H4 Cells Line
Journal: Pharmacogenomics & Personalized Medicine (2022) IF: 2.606
DOI: 10.2147/PGPM.S356326
Product Cited: Fetal Bovine Serum, SHG-44 Cells Line, Human Umbilical Vein Endothelial Cells, U-87 MG Cells Line, DMEM (High glucose) Medium, U251 Cells Line, H4 Cells Line
