A673 Cells
USUSD$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).
一般資訊
| 說明 | The A673 cell line is a valuable resource in biological science. Derived from the muscle tissue of a 15-year-old female patient diagnosed with Ewings Sarcoma, this cell line exhibits a distinct polygonal morphology. Originally the cell line was thought to be derived from a rhabdomyosarcoma (RMS). One of the remarkable characteristics of A673 cells is their ability to produce several growth factors that possess oncogenic potential. These cells also secrete growth-inhibitory factors, providing a balanced environment for cellular growth regulation. Such properties make A673 cells an excellent model for investigating the interplay between tumour-promoting and tumour-suppressing factors. A673 cells have demonstrated tumorigenic potential, as they can induce tumour formation in immunosuppressed mice. Moreover, studies have identified hypermethylated promoters in cancer-related genes within the A673 cell line. These genetic alterations further contribute to its relevance in cancer research, offering a platform to explore epigenetic modifications and their impact on tumour development and progression. While A673 cells are often referred to as Ewing tumour (ET) or sarcoma (ES), they are also associated with rhabdomyosarcoma (RMS). Notably, the A673 cell line harbours a complex karyotype with a specific translocation involving chromosomes 11 and 22. This translocation leads to the fusion of the EWS and FLI1 genes, which is a characteristic genetic event in Ewing Tumor. |
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| 生物體 | Human |
| 組織 | Bone |
| 疾病 | Ewing's Sarcoma |
| 同義詞 | A-673, RMS 1598, RMS1598 |
特徵
| 年齡 | 15 years |
|---|---|
| 性別 | Female |
| 族裔 | Caucasian |
| 形態學 | Fibroblast-like |
| 生長特性 | Monolayer, adherent |
監管數據
| 引用 | A673 (Cytion catalog number 300454) |
|---|---|
| 生物安全等級 | 1 |
| NCBI_TaxID | 9606 |
| Cellosaurus 編號 | CVCL_0080 |
生物分子資料
| 致瘤性 | Yes, in immunosuppressed mice |
|---|---|
| 對病毒的易感性 | Highly sensitive to human adenoviruses |
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) |
|---|---|
| 營養補充品 | Supplement the medium with 10% FBS |
| 解離試劑 | Accutase |
| 倍增時間 | 28 hours |
| 傳代培養 | 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. |
| 播種密度 | 1 x 104 cells/cm2 will result in a confluent monolayer within 8 days. |
| 流體更新 | 2 to 3 times per week |
| 解凍後的恢復 | 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. |
| 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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分析證明書 (CoA)
| 批次編號 | 證書類型 | 日期 | 型號 |
|---|---|---|---|
| 300454-3d21 | 分析證明書 | 26. May. 2025 | 300454 |