M2-10B4 Cells
USD$550.00*
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 M2-10B4 cell line is a clone derived from bone marrow stromal cells from a (C57BL/6J X C3H/HeJ)F1 mouse. These stromal cells are essential components of the bone marrow microenvironment and play a significant role in supporting hematopoiesis. The M2-10B4 cells are particularly valuable for research focused on the interactions between stromal and hematopoietic cells, as they can support both human and murine myelopoiesis in long-term culture. Additionally, these cells can sustain certain murine stromal cell-dependent pre-B cell lines in vitro, making them a versatile tool in hematopoietic research. The M2-10B4 cells express important extracellular matrix components such as laminin and collagen IV, which contribute to their ability to support hematopoietic cells. However, they do not express collagen I or Factor VIII, which distinguishes them from other stromal cell lines. The presence of laminin and collagen IV is critical for the maintenance of the bone marrow microenvironment, influencing cell adhesion, differentiation, and signaling pathways. Researchers often utilize the M2-10B4 cell line in co-culture systems to explore the effects of stromal cells on the behavior of hematopoietic progenitors, particularly in the context of bone marrow physiology and disease models. Given their origin and functional properties, M2-10B4 cells are an essential model for studying the bone marrow niche, especially in relation to hematological disorders such as leukemia. They are also useful in drug screening and the development of therapeutic strategies targeting the bone marrow microenvironment. |
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| Organism | Mouse |
| Tissue | Bone marrow |
| Synonyms | M210B4 |
Characteristics
| Breed/Subspecies | C57BL/6J x C3H/HeJ |
|---|---|
| Age | Unspecified |
| Gender | Female |
| Morphology | Fibroblast-like |
| Cell type | Fibroblast |
| Growth properties | Adherent |
Regulatory Data
| Citation | M2-10B4 (Cytion catalog number 400428) |
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| Biosafety level | 1 |
| NCBI_TaxID | 10090 |
| CellosaurusAccession | CVCL_5794 |
Biomolecular Data
| Products | Laminin, collagen IV (Collagen I(-), Factor VIII(-). |
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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) |
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| 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 |
| Fluid renewal | 2 to 3 times per week |
| Post-Thaw Recovery | Viability may be low after thawing. |
| 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 |
|---|---|---|---|
| 400428-060226 | Certificate of Analysis | 13. Mar. 2026 | 400428 |
| 400428-813 | Certificate of Analysis | 23. May. 2025 | 400428 |