CL-0101
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Product Introduction
| Cell Name | Hela |
| Synonyms | HELA;Hela;He La;He-La;Henrietta Lacks cells;Helacyton gartleri |
| Cellosaurus Accession | CVCL_0030 |
| Organism | Human |
| Growth Properties | Adherent |
| Morphology | Epithelial-like |
| Disease | cervical cancer cells |
| Tissue | Uterus; Cervix |
| Age | 31Y |
| 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 | 1:2-1:4 |
| 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 | 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 | HeLa cells are the first aneuploid, epithelial-like cell line derived from human tissue and maintained in continuous culture. They were established in 1951 by G.D. Gey et al. from cervical cancer tissue of a 31-year-old African American woman. Following re-examination of original tissue sections, Jones et al. diagnosed the tumor as adenocarcinoma. The cell line harbors human papillomavirus type 18 (HPV-18) sequences and must be handled in a Class II biosafety cabinet. HeLa cells are positive for keratin, express low levels of p53, and exhibit normal levels of pRb (retinoblastoma tumor suppressor protein). |
| Gene Expression | Lysophosphatidylcholine (lyso-PC) induces AP-1 activity and c-jun N-terminal kinase activity (JNK1) by a protein kinase C-independent pathway. The cells are positive for keratin by immunoperoxidase staining. |
| Biosafety Level | BSL-2 |
Documents
Publications
Journal: Scientific Reports (2025) IF: 3.9
DOI: 10.1038/s41598-025-08727-3
Product Cited: C-33 A Cells Line, Hela Cells Line
Journal: Scientific Reports (2025) IF: 3.8
DOI: 10.1038/s41598-025-95851-9
Product Cited: 293T [HEK-293T] Cells Line, Hela Cells Line
Journal: ANALYST (2025) IF: 3.6
DOI: 10.1039/D5AN00203F
Product Cited: Hela Cells Line
Journal: DEVELOPMENT (2025) IF: 3.6
DOI: 10.1242/dev.204761
Product Cited: Hela Cells Line, 293T Cells Line, COS-7 Cells Line
Journal: ACS Chemical Biology (2025) IF: 3.5
DOI: 10.1021/acschembio.5c00155
Product Cited: 50 mg/mL G-418 Solution, Hela Cells Line, L Wnt-3A Cells Line, PA-1 Cells Line
