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CFBE41o- 6.2 DeltaF508-CFTR Human Cell line

MILLIPORE SIGMA

ITEM#: 3042-SCC161

MFR#: SCC161

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

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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

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Product Name	Description	Item#	QTY
CFBE41o- 4.7 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-SCC159	EA	Add to Cart
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	Add to Cart
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	3042-SCC160	EA	Add to Cart
HL-60 DeltaF508-CF Human Promyelocytic Cell Line	Cystic fibrosis (CF) is caused by mutations in the CFTR gene, which encodes a chloride and bicarbonate ion channel (1). Among the approximately 150 known disease-causing mutations in CFTR, deletion of the phenylalanine-508 codon (DeltaF508) is the mo	3042-SCC251	EA	Add to Cart
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	Add to Cart