NCI-H2009 Cells
USD 540.00*
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).
Información general
| Descripción | The NCI-H2009 cell line is derived from a human non-small cell lung carcinoma (NSCLC), specifically an adenocarcinoma. This cell line is extensively used in lung cancer research to study the molecular and cellular mechanisms underlying adenocarcinoma, the most common subtype of NSCLC. NCI-H2009 cells are valuable for investigating genetic mutations, signal transduction pathways, and therapeutic responses associated with lung adenocarcinoma. NCI-H2009 cells exhibit an epithelial morphology and express markers characteristic of lung adenocarcinoma, including cytokeratins and carcinoembryonic antigen (CEA). They harbor genetic alterations frequently observed in NSCLC, such as mutations in the KRAS gene, which is pivotal in cell signaling, growth, and survival. Researchers utilize NCI-H2009 cells to explore key signaling pathways involved in lung cancer progression, such as the EGFR, KRAS, and PI3K/Akt pathways. These cells are also employed in high-throughput drug screening assays and preclinical testing of chemotherapeutic agents, targeted therapies, and immunotherapies. Additionally, NCI-H2009 cells are used to study mechanisms of drug resistance and to develop strategies to overcome it. The relevance of the NCI-H2009 cell line in lung adenocarcinoma research highlights its importance in advancing our understanding of lung cancer biology and in developing new and more effective treatment approaches for patients with NSCLC. |
|---|---|
| Organismo | Human |
| Tejido | Lung |
| Enfermedad | Adenocarcinoma |
| Lugar de metástasis | Lymph node |
| Sinónimos | H2009, H-2009, NCIH2009 |
Características
| Edad | 68 years |
|---|---|
| Género | Female |
| Origen étnico | European |
| Morfología | Epithelial |
| Propiedades de crecimiento | Adherent |
Datos normativos
| Referencia | NCI-H2009 (Cytion catalog number 305283) |
|---|---|
| Nivel de bioseguridad | 1 |
| NCBI_TaxID | 9606 |
| N.º de acceso de Cellosaurus | CVCL_1514 |
Datos biomoleculares
| Virus | Transformant: Epstein-Barr virus (EBV) |
|---|---|
| Perfil mutacional | Mutation: B2M, p.Met1Val (c.1A>G), heterozygous; Mutation: B2M, p.Gln28Ter (c.82C>T), heterozygous; Mutation: KRAS, p.Gly12Ala (c.35G>C), heterozygous; Mutation: TERT, c.1-124C>T (c.228C>T) (C228T); Mutation: TP53, p.Arg273Leu (c.818G>T), homozygous |
Manejo
| Medio de cultivo | HITES medium supplementedThe base medium for this cell line is DF12. To make the complete growth medium, add the following components to the base medium:
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|---|---|
| Reactivo de disociación | Accutase |
| Subcultivo | 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. |
| Renovación de fluidos | 2 to 3 times per week |
| Medio de congelación | 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. |
| Descongelación y cultivo de células |
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| Atmósfera de incubación | 37°C, 5% CO2, humidified atmosphere. |
| Condiciones de envío | 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. |
| Condiciones de almacenamiento | 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. |
Control de calidad y análisis molecular
| Esterilidad | 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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Certificado de análisis (CoA)
| Número de lote | Tipo de certificado | Fecha | Número de catálogo |
|---|---|---|---|
| 305283-020126 | Certificado de análisis | 03. Feb. 2026 | 305283 |
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