- ￥1380 - 2080
- 艾普蒂
- 武汉
- PA1000-9537
- 2025年07月13日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
Store at -20°C/-80°C upon receipt
- 保质期：
Generally, the shelf life of liquid form is 6 months at -20℃/-80℃. The shelf life of lyophilized form is 12 months at -20℃/-80℃.
- 英文名：
Cystic fibrosis transmembrane conductance regulator
- 库存：
50支
- 供应商：
艾普蒂
- 规格：
20μg/50μg
| 规格： | 20μg | 产品价格： | ￥1380.0 |
|---|---|---|---|
| 规格： | 50μg | 产品价格： | ￥2080.0 |
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文献和实验The pilocarpine sweat test, and in vivo assessment of CFTR function via nasal potential difference or intestinal current measurement are important tools to confirm the diagnosis of CF in subjects with suggestive symptoms. Since these tests
The use of human bronchial epithelial (HBE) cell cultures derived from the bronchi of CF patients offers the opportunity to study the effects of CFTR correctors and potentiators on CFTR function and epithelial cell biology in the native
CFTR Degradation and Aggregation
Defective protein folding is becoming increasingly recognized as a significant cause of human disease, and cystic fibrosis (CF) is a prime example. A number of CF-causing mutations in the cystic fibrosis transmembrane conductance regulator (CFTR
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