MC3T3-E1 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 | MC3T3-E1 is a pre-osteoblastic cell line derived from the calvaria of a mouse embryo. These cells are extensively utilized in the study of osteogenesis, particularly for examining the molecular and cellular mechanisms underlying bone formation and differentiation. The MC3T3-E1 cell line is known for its robust ability to differentiate into osteoblasts in vitro, a process that can be stimulated by ascorbic acid and beta-glycerophosphate. This differentiation is marked by the expression of key osteogenic markers such as alkaline phosphatase, osteocalcin, and type I collagen. MC3T3-E1 cells are instrumental in research focused on bone biology, including the study of bone matrix deposition and mineralization. These cells provide a reliable model for investigating the effects of various drugs, hormones, and genetic modifications on osteoblast function and bone formation. Additionally, the MC3T3-E1 cell line is valuable in studying pathological conditions such as osteoporosis and other bone-related diseases. Their ease of culture and well-characterized response to osteogenic stimuli make them a preferred choice for researchers aiming to unravel the complexities of bone physiology and pathology. |
|---|---|
| Organism | Mouse |
| Tissue | Bone, calvaria |
| Applications | In vitro osteoblast differentiation |
| Synonyms | Mc3T3-E1, MC3T3E1, MC-3T3-E1, MC 3T3-E1 |
Characteristics
| Breed/Subspecies | C57BL/6 |
|---|---|
| Age | 1 day |
| Gender | Unspecified |
| Morphology | Fibroblast-like |
| Cell type | Osteoblast |
| Growth properties | Adherent |
Regulatory Data
| Citation | MC3T3-E1 (Cytion catalog number 305187) |
|---|---|
| Biosafety level | 1 |
| NCBI_TaxID | 10090 |
| CellosaurusAccession | CVCL_0409 |
Biomolecular Data
| Tumorigenic | Yes, in immunodeficient mice |
|---|---|
| Products | Collagen |
Handling
| Culture Medium | Alpha MEM, w: 2.0 mM stable Glutamine, w: Ribonucleosides, w: Deoxyribonucleosides, w: 1.0 mM Sodium pyruvate, w: 2.2g/L NaHCO3, w/o: Ascorbic acid (GIBCO, Catalog No. A1049001. We do not supply this product; please consider other suppliers. Please let us know if you need further assistance.) |
|---|---|
| Supplements | Supplement the medium with 10% FBS |
| Dissociation Reagent | Accutase |
| Doubling time | 24 to 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 |
|---|---|---|---|
| 305187-080224 | Certificate of Analysis | 23. May. 2025 | 305187 |