ND7/23 Cells
USUSD$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).
一般資訊
| 說明 | The ND7/23 cell line is an immortalized hybrid derived from the fusion of neonatal rat dorsal root ganglion (DRG) neurons with a mouse neuroblastoma (N18TG2). This cell line retains numerous characteristics of sensory neurons and is frequently utilized to study neurobiological processes such as nociception, neuroregeneration, and neurite outgrowth. ND7/23 cells are a versatile model for understanding the cellular and molecular mechanisms of sensory neuron function, especially the pathways involved in nerve injury and repair. They express several sensory and nociceptor-related receptors, ion channels, and enzymes, making them suitable for a variety of applications in neuroscience. ND7/23 cells are widely used in research involving the differentiation of sensory neurons, often induced by factors like nerve growth factor (NGF) or dibutyryl cAMP (db-cAMP). Differentiated cells develop neurites, express neurofilament proteins, and show enhanced expression of molecules associated with nociceptive signaling, such as transient receptor potential (TRP) channels, including TRPC4. These features allow ND7/23 cells to serve as a model for studying the effects of neurotrophic factors and for screening potential neurotherapeutic agents. The cell line also facilitates high-throughput assays for analyzing calcium dynamics, electrophysiological properties, and drug responses in sensory neurons. In studies of nerve injury, ND7/23 cells have provided insights into the role of TRPC channels, particularly TRPC4, in axonal regeneration. Knockdown experiments using short hairpin RNA (shRNA) targeting TRPC4 have shown reduced neurite outgrowth, highlighting the importance of this channel in neuronal repair mechanisms. Additionally, ND7/23 cells offer an accessible and reproducible system for investigating signal transduction pathways and cellular responses to external stimuli, including neurotoxins and analgesics. |
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| 生物體 | Rat, Mouse |
| 組織 | Brain |
| 同義詞 | ND7-23 |
特徵
| 細胞類型 | Mouse Neuroblastoma Cells (N18 tg 2) x Rat Dorsal Root Ganglion Neurone Cells |
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| 生長特性 | Adherent |
監管數據
| 引用 | ND7/23 (Cytion catalog number 305520) |
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| 生物安全等級 | 1 |
| NCBI_TaxID | 10090, 10116 |
| Cellosaurus 編號 | CVCL_4259 |
生物分子資料
處理方式
| 培養基 | 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) |
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| 營養補充品 | Supplement the medium with 10% FBS |
| 播種密度 | 1 - 3 x 104 cells/cm2 |
| 冷凍培養基 | 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. |
| 細胞解凍與培養 |
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| 培養環境 | 37°C, 5% CO2, humidified atmosphere. |
| 運送條款 | 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. |
| 儲存條件 | 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. |
品質控制與分子分析
| 不孕症 | 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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