CFBE41o- 6.2WT-CFTR Human CF Bronchial Epithelial

CFBE41o- 6.2 WT-CFTR Human CF Bronchial Epithelial Cell Line CFBE41o- 6.2 WT-CFTR human CF bronchial epithelial cell line is used to study the relationship between CFTR mRNA expression and Cl transport function. Cystic Fibrosis (CF) is a lethal autos

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Product Name	Description	Item#	QTY
CFBE41o- 4.7 WT-CFTR Human CF Bronchial Epithelial	Cystic Fibrosis (CF) is a lethal autosomal recessive disease caused by mutations in the CF transmembrane conductance regulator (CFTR) gene which functions as a cAMP-activated and phosphorylated-regulated Cl channel. The predominant mutation in the CF	3042-SCC158	EA
CFBE41o- Human CF Bronchial Epithelial Cell Line CFBE41o- human CF bronchial epithelial cell line was derived from a cystic fibrosis patient homozygous for the DeltaF508 CFTR mutation.	Cystic Fibrosis (CF) is a lethal autosomal recessive disease caused by mutations in the CF transmembrane conductance regulator (CFTR) gene which functions as a cAMP-activated and phosphorylated-regulated Cl channel. The predominant mutation in the CF	3042-SCC151	EA
Human Bronchial Epithelial Cells: HBEpC, adult	HBEpC provide an excellent model system to study all aspects of epithelial function and disease, particularly those related to airway viral infections, as well as tissue repair mechanisms, signaling changes and potential treatments relevant to lung i	3042-50205A	EA
16HBE14o-Human Bronchial Epithelial Cell Line	16HBE14o- is a human bronchial epithelial cell line isolated from a 1-year old male heart-lung patient and immortalized with the origin-of-replication defective SV40 plasmid (pSVori-). The cell line retains characteristic features of normal different	3042-SCC150	EA
CFBE41o- 6.2 DeltaF508-CFTR Human Cell line	Cystic Fibrosis (CF) is a lethal autosomal recessive disease caused by mutations in the CF transmembrane conductance regulator (CFTR) gene which functions as a cAMP-activated and phosphorylated-regulated Cl channel. The predominant mutation in the CF	3042-SCC161	EA

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CFBE41o- 6.2WT-CFTR Human CF Bronchial Epithelial

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