SW-1736 Cells
USD$800.00*
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 | SW-1736 is a human thyroid anaplastic carcinoma cell line, commonly used to study aggressive and poorly differentiated thyroid cancers. This cell line was initially derived from a patient with undifferentiated thyroid carcinoma, a rare but highly aggressive form of cancer characterized by its rapid progression and poor prognosis. The SW-1736 cell line has been employed extensively in cancer research due to its ability to replicate the highly malignant features of anaplastic thyroid cancer (ATC), including resistance to standard therapies such as chemotherapy and radiation. One prominent feature of the SW-1736 cell line is its frequent use in studies focusing on cell division abnormalities and tumor metastasis. Researchers have observed atypical cell division events, such as one-to-four cell divisions, which are indicative of the aggressive and uncontrollable growth patterns found in anaplastic thyroid carcinomas. Additionally, SW-1736 cells have been transfected with various reporter genes like-Luc, allowing for non-invasive in vivo imaging studies. These studies are often performed in mouse models to investigate the metastatic potential of thyroid cancer, particularly its spread to organs such as the lungs and bones. Moreover, SW-1736 has been used to explore potential treatment strategies, including the combined use of metformin with standard chemotherapy agents like etoposide and epirubicin. These studies suggest that metformin enhances the cytotoxic effects of these drugs, increasing the induction of apoptosis and necrosis in SW-1736 cells. This combination therapy has shown promise in reducing cancer cell migration and proliferation, potentially offering new therapeutic avenues for tackling aggressive thyroid cancers. |
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| Organism | Human |
| Tissue | Thyroidea |
| Disease | Squamous cell carcinoma |
| Synonyms | SW1736, SW 1736 |
Characteristics
| Age | 77 years |
|---|---|
| Gender | Female |
| Ethnicity | Caucasian |
| Morphology | Epithelial-like |
| Growth properties | Adherent |
Regulatory Data
| Citation | SW-1736 (Cytion catalog number 300453) |
|---|---|
| Biosafety level | 1 |
| NCBI_TaxID | 9606 |
| CellosaurusAccession | CVCL_3883 |
Biomolecular Data
| Mutational profile | V600E type BRAF Mutation |
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Handling
| Culture Medium | RPMI 1640, w: 2.0 mM stable Glutamine, w: 2.0 g/L NaHCO3 (Cytion article number 820700a) |
|---|---|
| Supplements | Supplement the medium with 10% FBS |
| Dissociation Reagent | 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. |
| 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 |
|---|---|---|---|
| 300453-090226 | Certificate of Analysis | 13. Mar. 2026 | 300453 |
| 300453-616SF | Certificate of Analysis | 23. May. 2025 | 300453 |
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