A72 Cells
USD$395.00*
Products are shipped frozen on dry ice in cryotubes. Each cryotube typically contains 3 × 106 cells for adherent lines or 5 × 106 cells for suspension lines (refer to the batch CoA for details).
General information
| Description | A72 cells are a canine fibrosarcoma cell line derived from a spontaneously occurring tumor in a dog. These cells are used primarily in veterinary oncology research to study the biology, behavior, and treatment responses of canine fibrosarcomas. Their relevance extends to comparative oncology studies, where insights gained from canine cancers can be applied to human cancer research due to the biological similarities between certain canine and human tumors. The A72 cell line exhibits an adherent, fibroblast-like morphology and is known for its aggressive growth in vitro. It has been utilized to investigate various aspects of cancer cell biology, including proliferation, metastasis, and tumor cell interactions with the extracellular matrix. These cells are particularly valuable for assessing the efficacy of chemotherapeutic agents and exploring new therapeutic strategies, including immunotherapy and targeted therapies. A72 cells also provide a useful model for studying the molecular pathways involved in tumor growth and progression, such as signaling through the PI3K/Akt, MAPK, and other related pathways. They are instrumental in understanding the genetic and molecular underpinnings of fibrosarcoma, which can help identify potential biomarkers for diagnosis and targets for treatment in both veterinary and human oncology. |
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| Organism | Canine |
| Tissue | Muscle |
| Disease | Carcinoma |
| Synonyms | A 72, A-72 |
Characteristics
| Breed/Subspecies | Golden Retriever |
|---|---|
| Age | 8 years |
| Gender | Female |
| Morphology | Fibroblast-like |
| Growth properties | Monolayer, adherent |
Regulatory Data
| Citation | A72 (Cytion catalog number 602398) |
|---|---|
| Biosafety level | 1 |
| NCBI_TaxID | 9615 |
| CellosaurusAccession | CVCL_3453 |
Biomolecular Data
| Virus susceptibility | Canine coronaviruses, canine adenovirus I, II, canine herpes viruses, canine parainfluenzavirus, canine parvovirus canine distemper virus, minute virus of canines |
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Handling
| Culture Medium | DMEM, w: 4.5 g/L Glucose, w: 4 mM L-Glutamine, w: 3.7 g/L NaHCO3, w: 1.0 mM Sodium pyruvate (Cytion article number 820300a) |
|---|---|
| Supplements | Supplement the medium with 10% FBS |
| Dissociation Reagent | Accutase |
| Doubling time | 24 hours |
| 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. |
| Seeding density | 2 x 104 cells/cm2 will result in a confluent monolayer within 3 days. |
| Fluid renewal | 2 to 3 times per week |
| Post-Thaw Recovery | 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. |
| Freeze medium | As a cryopreservation medium, we 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. |
| Thawing and Culturing Cells |
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| Incubation Atmosphere | 37°C, 5% CO2, humidified atmosphere. |
| Shipping Conditions | Cryopreserved cell lines are shipped on dry ice in validated, insulated packaging with sufficient refrigerant to maintain approximately −78 °C throughout transit. On receipt, inspect the container immediately and transfer vials without delay to appropriate storage. |
| Storage Conditions | For long-term preservation, place vials in vapor-phase liquid nitrogen at about −150 to −196 °C. Storage at −80 °C is acceptable only as a short interim step before transfer to liquid nitrogen. |
Quality Control & Molecular Analysis
| Sterility | Mycoplasma contamination is excluded using both PCR-based assays and luminescence-based mycoplasma detection methods. To ensure there is no bacterial, fungal, or yeast contamination, cell cultures are subjected to daily visual inspections. |
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Certificate of Analysis (CoA)
| Lot Number | Certificate Type | Date | Catalog Number |
|---|---|---|---|
| 602398-010925 | Certificate of Analysis | 05. Dec. 2025 | 602398 |
| 602398-515SF | Certificate of Analysis | 23. May. 2025 | 602398 |