Cytion293F-X Cells
US$ 500,00*
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).
Informações gerais
| Descrição | Cytion293F-X refers to a suspension-adapted human embryonic kidney cell line equivalent to HEK293F cells, derived from the original HEK293 lineage. These cells originate from human embryonic kidney tissue and have been adapted for growth in serum-free, chemically defined media under suspension culture conditions. This adaptation enables high-density growth in shaker flasks or bioreactors, making them particularly suitable for large-scale protein expression. Like other HEK293 derivatives, 293F-X cells retain the adenoviral E1A/E1B genomic integration that supports robust transgene expression. Cytion293F-X cells are optimized for transient transfection workflows, especially for the production of recombinant proteins, monoclonal antibodies, and viral vectors. They exhibit high transfection efficiency using chemical methods such as polyethyleneimine (PEI) or lipid-based reagents, and are capable of producing substantial protein yields within short timeframes. Their suspension growth and scalability allow for efficient upscaling from small laboratory volumes to industrial bioprocessing systems, while maintaining consistent expression performance. In addition to protein production, Cytion293F-X cells are widely used in virology and gene delivery research, including the generation of adeno-associated virus (AAV) and lentiviral particles. They maintain key characteristics of HEK293-derived systems, including human-like post-translational modification machinery, which is critical for proper protein folding and glycosylation. However, as with other HEK293 variants, genomic heterogeneity and clonal variation may influence expression outcomes, and optimization of culture and transfection parameters is often required for specific applications. |
|---|---|
| Organismo | Human |
| Tecido | Kidney |
| Doença | Normal human embryonic kidney (HEK293-derived; suspension-adapted; not tumorigenic in standard use) |
| Local da metástase | Not applicable (non-tumorigenic HEK293 derivative adapted for suspension culture) |
| Aplicações | Recombinant protein and antibody production; transient transfection host; AAV and lentiviral vector manufacturing; suspension bioreactor culture; scalable GMP-compatible expression systems; post-translational modification studies |
Características
| Idade | Fetus |
|---|---|
| Gênero | Female |
| Etnia | Not applicable (immortalized embryonic kidney cell line) |
| Morfologia | Epithelial-like |
| Tipo de célula | Epithelial cells (embryonic kidney) |
| Propriedades de crescimento | Suspension |
Dados regulatórios
| Referência | Cytion293F-X (Cytion catalog number 305927) |
|---|---|
| Nível de biossegurança | 1 |
| NCBI_TaxID | 9606 |
| Número de acesso do Cellosaurus | Not assigned (Cytion293F-X is a proprietary suspension-adapted HEK293F derivative; parental HEK293 CVCL_0045) |
| Situação em relação aos OGMs | GMO-S1: This Cytion293F-X cell line contains SV40, enabling high transfection efficiency and robust growth in suspension culture. The modification is stably present in embryonic kidney cells. This classification applies only within Germany and may differ elsewhere. |
Dados biomoleculares
| Receptores expressos | Vitronectin |
|---|---|
| Expressão de proteínas | CEA negative, p53 positive |
| Tumorigênico | In nude mice |
| Vírus | Transformed with adenovirus 5 DNA adenovirus 5 DNA |
Manuseio
| Meio de cultura | Expi293 Expression Medium |
|---|---|
| Reagente de dissociação | None |
| Subcultura | 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. |
| Densidade de semeadura | 0.3 to 1 x 106 cells/ml |
| Renovação de fluidos | 2 times per week |
| Recuperação pós-degelo | After thawing, plate the cells at 5 x 104 cells/cm2 and allow the cells to recover from the freezing process and to adhere for at least 24 hours. |
| Meio de congelamento | As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability. |
| Descongelamento e cultura de células |
|
| Atmosfera de incubação | 37°C, 5% CO2, humidified atmosphere. |
| Condições de envio | 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. |
| Condições de armazenamento | 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. |
Controle de Qualidade e Análise Molecular
Certificado de Análise (CoA)
| Número do lote | Tipo de certificado | Data | Número de catálogo |
|---|---|---|---|
| 305927-200326 | Certificado de Análise | 04. May. 2026 | 305927 |