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CFTR

An ATP-binding cassette (ABC) transporter superfamily member is encoded by this gene. The encoded protein regulates ion and water secretion and absorption in epithelial tissues and, unlike other members of this protein family, acts as a chloride channel. The cycles of ATP binding by the nucleotide-binding domains, regulatory domain phosphorylation, and ATP hydrolysis are what cause channel activation. Cystic fibrosis, the most prevalent deadly genetic illness among people of Northern European origin, is brought on by mutations in this gene.

Full Name CF transmembrane conductance regulator
Gene ID Human: 1080
Mouse: 12638
Rat: 24255
Monkey: 574346
UniProt ID Human: Q20BH0
Mouse: P26361
Rat: P34158
Monkey: Q00553
Alternative Names CF; MRP7; ABC35; ABCC7; CFTR/MRP; TNR-CFTR; dJ760C5.1; cystic fibrosis transmembrane conductance regulator; cAMP-dependent chloride channel; channel conductance-controlling ATPase; cystic fibrosis transmembrane conductance regulating; cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7); CFTR; CF transmembrane conductance regulator

Product List

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Magic™ mPro Human CFTR Cell Line [CAT#: S01YF-1122-KX77]

Product Category:
Membrane Protein Stable Cell Lines
Target Protein: CFTR Target Family: Chloride, Ligand-Gated Target Protein Species: Human
Product Category:
Membrane Protein Stable Cell Lines
Target Protein: CFTR Target Family: Chloride, Ligand-Gated Target Protein Species: Human
Product Category:
Membrane Protein Stable Cell Lines
Target Protein: CFTR Target Family: Cystic Fibrosis Transmembrane Conductance Regulator Target Protein Species: Human Host Cell Type: A2780; SKOV3; CHO-K1; HEK293
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