M-MSV-Balb/3T3 Cells
CAD$545.10*
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 M-MSV-Balb/3T3 cell line is a mouse fibroblast cell line derived from BALB/c mice. These cells are widely used in research due to their stable growth characteristics and well-characterized genetic background. They originate from the 3T3 cell line, which is a standard fibroblast cell line established from mouse embryonic tissue. The M-MSV-Balb/3T3 cells have been transformed by the Moloney Murine Sarcoma Virus (M-MSV), making them a valuable tool for studying viral oncogenesis, signal transduction pathways, and the molecular mechanisms underlying cellular transformation and tumorigenesis. The transformation by M-MSV endows these cells with a range of oncogenic properties, including increased proliferation rates, loss of contact inhibition, and the ability to form colonies in soft agar, which are hallmarks of malignant transformation. These features make M-MSV-Balb/3T3 cells particularly useful for in vitro studies on cancer biology, including the identification of oncogenes and tumor suppressor genes, as well as the testing of potential anticancer therapies. Additionally, their use in transfection experiments allows for the exploration of gene function and regulation in the context of a transformed phenotype. |
|---|---|
| Organism | Mouse |
| Tissue | Embryonic |
| Synonyms | M-MSV-BALB/3T3 |
Characteristics
| Breed/Subspecies | BALB/c |
|---|---|
| Age | Embryo, 14 to 17 day gestation |
| Gender | Female |
| Morphology | Fibroblast-like |
| Cell type | Fibroblast |
| Growth properties | Adherent |
Regulatory Data
| Citation | M-MSV-Balb/3T3 (Cytion catalog number 400458) |
|---|---|
| Biosafety level | 1 |
| NCBI_TaxID | 10090 |
| CellosaurusAccession | CVCL_5793 |
| GMO Status | GMO-S1: This murine fibroblast cell line (M-MSV-Balb/3T3) contains Moloney murine sarcoma virus (MOMSV) sequences introduced via transfection, without production of infectious virus, supporting transformed growth. The viral sequences are stably present in Balb/3T3-derived cells. This classification applies only within Germany and may differ elsewhere. |
Biomolecular Data
| Antigen expression | H-2d |
|---|---|
| Tumorigenic | Yes |
| Viruses | Ectromelia virus (mousepox): negative. |
| Reverse transcriptase | Negative |
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 |
| 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 | 0.7 to 1 x 106 cells/cm2 |
| 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 |
|---|---|---|---|
| 400458-33 to 320 | Certificate of Analysis | 18. Aug. 2025 | 400458 |