B82 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 | B82 cells were derived from mouse fatty tissue, growh adherently and show a fibroblast morphology, providing researchers with a versatile model to explore a wide range of scientific questions. B82 cells originate from NCTC clone 929, a cell line that underwent progressive selection in BUdR (bromodeoxyuridine). As a result, B82 cells demonstrate a high cloning efficiency of 70-80%, enabling researchers to generate a substantial number of genetically identical cells for their experiments. The karyotype of B82 cells is 2n = 51. B82 cells are a suitable experimental model for studying cellular behaviour, signalling pathways, and tissue engineering applications. With their high cloning efficiency, researchers can confidently explore a myriad of scientific questions. |
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| Organism | Mouse |
| Tissue | Skin |
| Synonyms | B82 (Hamprecht), B-82, GM00347, GM-347, GM0347, GM347, GM00347A, GM 0347A |
Characteristics
| Breed/Subspecies | C3H/An |
|---|---|
| Age | 100 days |
| Gender | Male |
| Morphology | Fibroblast |
| Growth properties | Adherent |
Regulatory Data
| Citation | B82 (Cytion catalog number 305173) |
|---|---|
| Biosafety level | 1 |
| NCBI_TaxID | 10090 |
| CellosaurusAccession | CVCL_4114 |
Biomolecular Data
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. |
| 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 |
|---|---|---|---|
| 305173-290724 | Certificate of Analysis | 23. May. 2025 | 305173 |