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當前位置：> 供求商機> a549-ascg——A549 human lung carcinoma - ASC-GFP reporter cells
當前位置：> 供求商機> a549-ascg——A549 human lung carcinoma - ASC-GFP reporter cells
貨物所在地：北京北京市
更新時間：2024-03-27 13:43:34
有效期：2024年3月27日 -- 2025年3月28日
已獲點擊：36
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Contents and Storage
• 3-7 x 106 A549-ASC cells in a cryovial or shipping flask IMPORTANT: If cells provided in a cryovial are not frozen upon arrival, contact InvivoGen immediately.
• 1 ml of Blasticidin(10 mg/ml). Store at 4°C or at -20°C.*
• 1 ml of Normocin™ (50 mg/ml), a formulation of three antibiotics active against mycoplasmas, bacteria and fungi. Store at -20°C.*
*The expiry date is specified on the product label. Handling Frozen Cells Upon Arrival Cells must be thawed immediately upon receipt and grown according to handling procedures (as described on the next page) to ensure the best cell viability and proper assay performance. Note: Avoid freezing cells upon receipt as it may result in irreversible damage to the cell line.
Disclaimer: We cannot guarantee cell viability if the cells are not thawed immediately upon receipt and grown according to handling procedures. IMPORTANT: For cells that arrive in a shipping flask please refer to the enclosed ‘cell recovery procedure’.
Cell Line Stability
Cells will undergo genotypic changes resulting in reduced responsiveness over time in normal cell culture conditions. Genetic instability is a biological phenomenon that occurs in all stably genetically engineered cells. Therefore, it is critical to prepare an adequate number of frozen stocks at early passages. To ensure maximum efficiency, do not passage A549-ASC cells more than 20 times.
Quality Control
• The induction of ASC::GFP expression has been verified by Western blot, fluorescence microscopy and flow cytometry.
• The stability of this cell line for 20 passages following thawing has been verified.
• A549-ASC cells are guaranteed mycoplasma-free.
Applications:
Screening of NLRP1 inflammasome activating stimuli
Real-time monitoring of ASC-dependent inflammasome assembly
Rapid and visual screening of drugs targeting the NLRP1 inflammasome by fluorescence microscopy
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