CL-0527
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Product Introduction
| Cell Name | COV434 |
| Synonyms | COV-434;COV 434 |
| Cellosaurus Accession | CVCL_2010 |
| Organism | Human |
| Growth Properties | Adherent with clustering |
| Morphology | Epithelial-like |
| Disease | ovarian cancer cells |
| Tissue | Ovary |
| Age | 26Y |
| Sex | Female |
| 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. At 24 h post-recovery, cells are not yet fully spread. Most cells remain as round, translucent cell clusters and are predominantly adherent. Occasionally, a small number of cell clusters may float; medium change is not required at this time. At 48 h post-recovery, cells attached to the bottom of the culture vessel will spread out and exhibit a cobblestone morphology. However, some round cell clusters may still adhere to the underlying cell monolayer. Medium change can be performed at this point. 4. During recovery, maintain an appropriate gas atmosphere and medium volume to ensure proper pH of the culture medium. Suboptimal conditions may prevent cell adherence. |
| Complete Medium | DMEM [PM150210]+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 | 5 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. |
| Biosafety Level | BSL-1 |
Documents
Publications
Journal: Gut Microbes (2024) IF: 12.2
DOI: 10.1080/19490976.2024.2412381
Product Cited: KGN Cells Line, COV434 Cells Line
Journal: Cell Death & Disease (2024) IF: 9
DOI: 10.1038/s41419-024-06540-w
Product Cited: KGN Cells Line, COV434 Cells Line
Journal: INTERNATIONAL IMMUNOPHARMACOLOGY (2024) IF: 4.8
DOI: 10.1016/j.intimp.2024.113513
Product Cited: THP-1 Cells Line, COV434 Cells Line
Journal: Journal of Ovarian Research (2024) IF: 4
DOI: 10.1186/s13048-024-01344-0
Product Cited: COV434 Cells Line, RAW 264.7 Cells Line
Journal: Journal of Ovarian Research (2024) IF: 4
DOI: 10.1186/s13048-024-01434-z
Product Cited: COV434 Cells Line, KGN Cells Line
