ME-180 cell

SKU:BHC11101086
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Overview
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ME-180 cell is a Epithelial cell line derived from Caucasian (Female). It is commonly used as an in vitro model for 2 research. Growth characteristics: Adherent, Epithelial-like. Supplied as cryopreserved cells with accompanying batch CoA and quality-control documentation.

Species Human
Disease model Epidermoid Carcinoma
Morphology Epithelial-like
Growth Properties Adherent
Tissue Uterus, Cervix
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Catalog no. Size
300196 1 cryovial
Available Options

This cell line is available in the U.S. For non-profit users, please sign and submit the Non-Profit Supply Agreement to orders@biohippo.com before placing an order. For commercial users, please complete the CLEAR Form before ordering, as additional usage fees may apply based on the intended use. For further details, please contact orders@biohippo.com. Products ship after the required agreement is completed; typical delivery is 2–3 business days. Products are shipped frozen on dry ice in cryotubes. Each cryotube typically contains 3 × 10^6 cells for adherent lines or 5 × 10^6 cells for suspension lines (refer to the batch CoA for details).

Field Specification
Mfr No 300196
Species Human
The ME-180 cell line is an epithelial cell line established from a highly invasive squamous cell carcinoma, originally isolated from the omental metastasis of a cervical carcinoma in a 66-year-old White female patient. The carcinoma was characterized by irregular cell clusters with no significant keratinization and minimal necrosis. This cell line is particularly significant for cancer research, especially in studies involving cervical cancer and other forms of squamous cell carcinoma, due to its origin and aggressive nature. ME-180 cells are tumorigenic and have been shown to form well-differentiated epidermoid carcinomas when implanted in nude mice. ME-180 cells have several unique properties, including a heteroploid karyotype with a subtriploid mode, indicating an unstable chromosomal arrangement. The cells exhibit typical epithelial morphology with numerous desmosomes and tonofibrils, and they do not exhibit contact inhibition, often leading to layered growth in culture. The cell line's growth is inhibited by tumor necrosis factor alpha (TNF alpha), making it useful for studies investigating the effects of inflammatory cytokines on tumor cells. Additionally, ME-180 cells contain human papillomavirus (HPV) DNA, with a higher homology to HPV-68 compared to HPV-18, which could be relevant for studies on HPV-related carcinogenesis. ME-180 cells are also valuable in infectious disease research due to their sensitivity to various viruses. The cell line has been used to study the interaction with several viruses, including influenza and myxoviruses. ME-180 cells have shown the ability to form persistent infections with some myxoviruses, making them a useful model for studying viral latency and the long-term effects of viral infection on cancer cells. The combination of its cancerous origin, viral susceptibility, and specific growth characteristics make ME-180 a versatile tool in both oncology and virology research.

SKU:BHC11101086

Viruses: HPV68 positive

  • cultureMedium: McCoys 5a, w: 3.0 g/L Glucose, w: stable Glutamine, w: 2.0 mM Sodium pyruvate, w: 2.2 g/L NaHCO3 (Cytion article number 820200a)
  • supplements: Supplement the medium with 10% FBS
  • dissociationReagent: Accutase
  • subculturing: Remove the old medium from the adherent cells and wash them with PBS that lacks calcium and magnesium. For T25 flasks, use 3-5 ml of PBS, and for T75 flasks, use 5-10 ml. Then, cover the cells completely with Accutase, using 1-2 ml for T25 flasks and 2.5 ml for T75 flasks. Let the cells incubate at room temperature for 8-10 minutes to detach them. After incubation, gently mix the cells with 10 ml of medium to resuspend them, then centrifuge at 300xg for 3 minutes. Discard the supernatant, resuspend the cells in fresh medium, and transfer them into new flasks that already contain fresh medium.
  • seedingDensity: 1 x 104 cells/cm2
  • fluidRenewal: 2 to 3 times per week
  • postThawRecovery: After thawing, plate the cells at 5 x 104 cells/cm2 and allow the cells to recover from the freezing process and to adhere for at least 24 hours.
  • freezeMedium: As a cryopreservation medium, use complete growth medium (including FBS) + 10% DMSO for adequate post-thaw viability, or CM-1 (Cytion catalog number 800100), which includes optimized osmoprotectants and metabolic stabilizers to enhance recovery and reduce cryo-induced stress.
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