3T6-Swiss albino 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 3T6-Swiss albino cell line originates from the tissue of Swiss albino mice, specifically developed for a broad range of virological and oncological research purposes. This fibroblast cell line is known for its susceptibility to various viruses, including murine sarcoma viruses, making it an invaluable tool in the study of viral oncogenesis and the transformational properties of oncogenes in a controlled environment. The robustness of 3T6-Swiss albino cells in culture allows for detailed genetic manipulation and analysis, facilitating advanced genetic studies that seek to understand the intricacies of cancer progression and viral infection mechanisms. In addition to its applications in virology, the 3T6-Swiss albino cell line is frequently used in pharmacological research. Its responsiveness to pharmaceutical agents makes it a suitable model for drug screening and toxicity testing. Researchers utilize these cells to examine the cellular responses to new compounds, evaluating their efficacy and safety before proceeding to more complex in vivo studies. The genetic stability of the 3T6-Swiss albino cell line over multiple passages supports consistent experimental results, which is crucial for the development of reliable therapeutic strategies. |
|---|---|
| Organism | Mouse |
| Tissue | Embryonic |
| Applications | This cell line is an optimal choice for transfection. |
| Synonyms | 3T6 Swiss Albino, Swiss 3T6, NIH 3T6, 3T6, GM05862 |
Characteristics
| Age | Embryo |
|---|---|
| Morphology | Fibroblast-like |
| Cell type | Fibroblast |
| Growth properties | Adherent |
Regulatory Data
| Citation | 3T6-Swiss albino (Cytion catalog number 400104) |
|---|---|
| Biosafety level | 1 |
| NCBI_TaxID | 10090 |
| CellosaurusAccession | CVCL_0601 |
Biomolecular Data
| Tumorigenic | No |
|---|---|
| Viruses | Negative for ectromelia virus (mousepox). |
| Virus susceptibility | Herpes simplex, Vaccinia, Pseudorabies, Vesicular Stomatitis (Indiana) |
| Reverse transcriptase | Negative |
| Products | Collagen, hyaluronic acid |
| Ploidy status | Karyotyping results revealed an unstable range of 78-81. A significant portion (21%) of the cells contained a terminal centromere on a large chromosome, and another 21% comprised minuscule chromosomes. |
Handling
| Culture Medium | Ham's F12, w: 1.0 mM stable Glutamine, w: 1.0 mM Sodium pyruvate, w: 1.1 g/L NaHCO3 (Cytion article number 820600a) |
|---|---|
| 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. |
| Seeding density | 1 x 104 cells/cm2 will result in a confluent monolayer within 5 days. |
| Fluid renewal | Every 3 to 4 days |
| 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 48 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 |
|
| 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. |
|---|
Certificate of Analysis (CoA)
| Lot Number | Certificate Type | Date | Catalog Number |
|---|---|---|---|
| 400104-080125 | Certificate of Analysis | 18. Aug. 2025 | 400104 |