CL-0210
$ 420.00
Select a size
Quantity
In stock
InquireFor order requirements and technical needs, please Contact Us
Product Introduction
| Cell Name | SiHa |
| Synonyms | Siha;SIHA |
| Cellosaurus Accession | CVCL_0032 |
| Organism | Human |
| Growth Properties | Adherent |
| Morphology | Epithelial-like |
| Disease | cervical cancer cells |
| Tissue | Uterus, cervix |
| Age | 55Y |
| 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. |
| Complete Medium | MEM, with NEAA [PM150410]+10% Nutrient+1% Supplement |
| Incubation Atmosphere | Air, 95%; CO₂, 5% |
| Temperature | 37℃ |
| Subcultivation Ratio | 1:3-1:8 |
| 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 | SiHa cells were established from a primary surgical tissue sample from a Japanese patient. Electron microscopy reveals typical desmosomes at intercellular junctions and abundant tonofilaments in the cytoplasm. In nude mice, SiHa cells form poorly differentiated epidermoid carcinoma (grade III).The oncogenes PRB and p53 are positive in SiHa cells. |
| Tumorigenic | Yes, in nude mice; forms poorly differentiated epidermoid carcinoma (grade III). |
| Gene Expression | Oncogenes: p53+; pRB+ |
| Biosafety Level | BSL-2 [Cells contain human papilloma virus] |
Documents
Publications
Journal: BMC CANCER (2025) IF: 3.4
DOI: 10.1186/s12885-025-14637-4
Product Cited: Ca Ski Cells Line, SiHa Cells Line
Journal: BMC CANCER (2025) IF: 3.4
DOI: 10.1186/s12885-025-14920-4
Product Cited: SiHa Cells Line, Hela Cells Line
Journal: BMC CANCER (2025) IF: 3.4
DOI: 10.1186/s12885-025-15099-4
Product Cited: C-33 A Cells Line, Hela Cell Complete Medium, SiHa Cells Line, C-33 A Cell Complete Medium, Hela Cells Line, Ca Ski Cells Line, SiHa Cell Complete Medium, Ca Ski Cell Complete Medium
Journal: Frontiers in Bioscience-Landmark (2025) IF: 3.3
DOI: 10.31083/FBL26756
Product Cited: Ca Ski Cells Line, SiHa Cells Line, Fetal Bovine Serum
Journal: Journal of Cancer (2025) IF: 3.3
DOI: 10.7150/jca.87027
Product Cited: SiHa Cells Line
