B16-F10 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).
Key points about B16-F10 cells
| Description | The B16-F10 cell line is a subline of the murine B16 melanoma cell line, derived from a spontaneous skin tumor in a mouse. These cells are characterized by their aggressive metastatic potential, particularly to the lungs, making them a valuable model for studying melanoma progression and metastasis. The B16-F10 cells exhibit high melanin content, which contributes to their pigmentation and is used as a marker in various assays to track cell proliferation and tumor growth. B16-F10 was obtained through a ten-time selective procedure using Fidler's method, enhancing its metastatic capability compared to its parent line, B16-F0, and the B16-F1 subline, which underwent a one-time selective procedure. B16-F10 cells are widely used in cancer research due to their ability to form tumors in syngeneic C57BL/6 mice, providing a consistent and reproducible model for in vivo studies. These cells express various melanoma-associated antigens, which are crucial for investigating immune responses and developing immunotherapies. Additionally, B16-F10 cells are used to evaluate the efficacy of chemotherapeutic agents and the molecular mechanisms underlying drug resistance in melanoma. The cell line's genetic profile and behavior under different experimental conditions offer insights into the pathways involved in melanoma metastasis, aiding in the development of targeted therapeutic strategies. It is noteworthy that B16-F10's derivative, B16-BL6, exhibits even greater invasive activity, making the B16 series a comprehensive model system for studying different aspects of melanoma biology and therapy. |
|---|---|
| Organism | Mouse |
| Tissue | Skin |
| Disease | Mouse melanoma |
| Synonyms | B16/F10, B16 F10, B16F10, B16 melanoma F10 |
Features of the B16-F10 cell line
| Breed/Subspecies | C57BL/6 |
|---|---|
| Gender | Male |
| Morphology | Mixture of spindle-shaped and epithelial-like cells |
| Growth properties | Adherent |
Specifications
| Citation | B16-F10 (Cytion catalog number 305157) |
|---|---|
| Biosafety level | 1 |
| NCBI_TaxID | 10090 |
| CellosaurusAccession | CVCL_0159 |
Genetic profile of the B16 melanoma model
| Products | Melanin |
|---|
Culturing methods
| 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 |
| 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 verification
| 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 |
|---|---|---|---|
| 305157-250725 | Certificate of Analysis | 18. Aug. 2025 | 305157 |
| 305157-030323SF | Certificate of Analysis | 23. May. 2025 | 305157 |
| 305157-131124 | Certificate of Analysis | 23. May. 2025 | 305157 |
| 305157-030323 | Certificate of Analysis | 23. May. 2025 | 305157 |
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