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- BGT-KET-13665
- 2025年07月13日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
100
- 供应商：
艾美捷科技
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Human CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) ELISA试剂盒，Human CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) ELISA Kit，Human CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) ELISA Kit,Human CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) ELISA Kit
产品名称：Human CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) ELISA试剂盒-Human CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) ELISA Kit
产品货号：BGT-KET-13665
产品规格：96wells
Human CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) ELISA Kit,Human CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) ELISA Kit
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文献和实验A suspension array hybridization assay is described for the detection of 31 mutations and polymorphisms in the cystic fibrosis transmembrane conductance regulator (CFTR) gene using Luminex� xMAP™ technology. The Luminex xMAP system allows
degradation of the cystic fibrosis transmembrane conductance regulator (CFTR). The experimental system described employs transiently transfected HEK-293 cells and is utilized to monitor the biogenesis of CFTR by Western blot and pulse-chase analysis.
Cystic fibrosis (CF) is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR ) gene (1 ,2 ). More than 1000 disease mutations and 200 polymorphisms have been identified in the CFTR gene (3 ). The type
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