CL-0155
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Product Introduction
| Cell Name | ME-180 |
| Synonyms | Me-180;ME 180;ME180 |
| Cellosaurus Accession | CVCL_1401 |
| Organism | Human |
| Growth Properties | Adherent |
| Morphology | Epithelial-like |
| Disease | cervical cancer cells |
| Tissue | Uterus; Cervix; derived from metastatic site: omentum |
| Age | 66Y |
| Sex | Female |
| Instructions | 1. Check all containers for leakage or breakage.<br/> 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 | McCoy's 5A [PM150710]+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 | 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 ME-180 cell line was established from invasive squamous cell carcinoma, which presents irregular cell aggregates with negligible keratinization. Zonulae adherentes can be observed between adjacent ME-180 cells in monolayer culture, along with cytoplasmic tonofilaments. This cell line was found to be mycoplasma-contaminated in 1970, and the contamination was later eliminated. Tumor necrosis factor-alpha (TNF-α) can suppress the proliferation of ME-180 cells. Furthermore, ME-180 cells harbor human papillomavirus (HPV) DNA, which shares higher sequence homology with HPV-39 than HPV-18. |
| Tumorigenic | Yes, in nude mice; forms well differentiated epidermoid carcinoma (grade I). |
| Antigen Expression | Blood Type A; Rh+; HLA A1, A11, B5(+/-), B40 |
| Gene Expression | Oncogenes: p53+; pRB+ |
| Biosafety Level | BSL-2 |
Documents
Publications
Journal: CANCER SCIENCE (2026) IF: 4.3
DOI: 10.1111/cas.70305
Product Cited: Ca Ski Cells Line, Human Cervical Epithelial Cells (Primary cell immortalization), SiHa Cells Line, Hela Cells Line, C-33 A Cells Line, ME-180 Cells Line
Journal: APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY (2026) IF: 3.3
DOI: 10.1007/s12010-026-05607-y
Product Cited: Hela Cells Line, SiHa Cells Line, MS751 Cells Line, HCC1428 Cells Line, C-33 A Cells Line, ME-180 Cells Line, Ca Ski Cells Line
Journal: PLoS One (2026) IF: 2.6
DOI: 10.1371/journal.pone.0343495
Product Cited: Hela Cells Line, Ca Ski Cells Line, SiHa Cells Line, ME-180 Cells Line
Journal: PATHOLOGY RESEARCH AND PRACTICE (2025) IF: 3.2
DOI: 10.1016/j.prp.2025.156096
Product Cited: C-33 A Cells Line, ME-180 Cells Line, SiHa Cells Line, Hela Cells Line
Journal: iScience (2023) IF: 5.8
DOI: 10.1016/j.isci.2023.107315
Product Cited: ME-180 Cells Line
