BS-C-1 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 | The BS-C-1 cell line, also known as Cercopithecus aethiops kidney cells, originates from the kidney of the African green monkey. This cell line, established in the 1960s, is used extensively in virology research due to its susceptibility to adenoviruses, simian viruses, and other pathogenic agents. BS-C-1 cells exhibit epithelial morphology and are adherent in culture, making them suitable for a variety of experimental setups, including virus-host interaction studies and cytotoxicity assays. One of the distinguishing features of BS-C-1 cells is their utility in the propagation and maintenance of polioviruses, which facilitates vaccine development and virus lifecycle studies. The cells are also known for their role in the discovery and study of adenoviruses, contributing significantly to our understanding of viral genetics and replication processes. Despite their origins and primary uses, BS-C-1 cells have also been employed in pharmacological research and toxicology, testing the effects of various substances on cellular processes and viability. Due to their robust growth characteristics and ability to be transfected relatively easily, BS-C-1 cells are valuable in molecular biology for gene expression studies. Their compatibility with a wide range of DNA transfection methods supports their use in gene therapy research and recombinant protein production. Overall, BS-C-1 cells continue to be a critical resource in biomedical research, providing insights into cellular behavior and the molecular basis of disease. |
|---|---|
| Organism | Chlorocebus pygerythrus (Vervet monkey) |
| Tissue | Kidney |
| Synonyms | BSC-1, BSC1, GMK, Biologics Standards-Cercopithecus-1 |
Characteristics
| Morphology | Epithelial |
|---|---|
| Growth properties | Adherent |
Regulatory Data
| Citation | BS-C-1 (Cytion catalog number 305009) |
|---|---|
| Biosafety level | 1 |
| NCBI_TaxID | 9534 |
| CellosaurusAccession | CVCL_0607 |
Biomolecular Data
| Protein expression | Keratin |
|---|
Handling
| Culture Medium | EMEM (MEM Eagle), w: 2 mM L-Glutamine, w: 2.2 g/L NaHCO3, w: EBSS (Cytion article number 820100a) |
|---|---|
| Supplements | Supplement the medium with 10% FBS and 1% NEAA |
| Dissociation Reagent | Accutase |
| Doubling time | 72 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 |
|
| Incubation Atmosphere | 37°C, 5% CO2, humidified atmosphere. |
| Flask Coating | None |
| 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. |
|---|
Certificate of Analysis (CoA)
| Lot Number | Certificate Type | Date | Catalog Number |
|---|---|---|---|
| 305009-220525 | Certificate of Analysis | 23. Jan. 2026 | 305009 |
| 305009-110423 | Certificate of Analysis | 22. Jan. 2026 | 305009 |