KTC-1 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 | The KTC-1 cell line is a well-characterized human thyroid carcinoma cell model derived from an adult patient with poorly differentiated thyroid carcinoma. This cell line is particularly valuable in research focused on the aggressive forms of thyroid cancer, including anaplastic thyroid carcinoma (ATC), due to its origins from a cancer type that is known for rapid progression and resistance to conventional therapies. The KTC-1 cells exhibit a spindle-shaped morphology, consistent with epithelial-to-mesenchymal transition (EMT), which is a hallmark of highly invasive cancers. These cells are known to have mutations in key oncogenes and tumor suppressor genes, including BRAF and TP53, which contribute to their malignant phenotype. KTC-1 cells are a useful model for studying the molecular mechanisms underlying thyroid cancer progression, including signaling pathways such as MAPK/ERK and PI3K/AKT, which are often dysregulated in aggressive thyroid cancers. They are also employed in drug screening assays to evaluate the efficacy of novel therapeutic agents targeting these pathways. Additionally, KTC-1 cells have been utilized in research exploring the tumor microenvironment, particularly the interactions between cancer cells and stromal cells that may influence tumor growth and metastasis. Due to their well-documented genetic and phenotypic characteristics, KTC-1 cells provide a robust platform for translational research aimed at developing more effective treatment strategies for aggressive thyroid carcinomas. |
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| Organism | Human |
| Tissue | Thyroid |
| Disease | Thyroid carcinoma |
| Metastatic site | Pleural effusion |
| Synonyms | KTC1, KTC1naive |
Characteristics
| Age | 68 years |
|---|---|
| Gender | Male |
| Morphology | Epithelial |
| Growth properties | Adherent |
Regulatory Data
| Citation | KTC-1 (Cytion catalog number 305113) |
|---|---|
| Biosafety level | 1 |
| NCBI_TaxID | 9606 |
| CellosaurusAccession | CVCL_6300 |
Biomolecular Data
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 | 48 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. |
| Fluid renewal | 2 to 3 times per week |
| 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 |
|---|---|---|---|
| 305113-250624 | Certificate of Analysis | 23. May. 2025 | 305113 |