CFTR: Products

Cystic fibrosis transmembrane conductance regulator (CFTR) is a multi-pass transmembrane protein that functions as a chloride channel. CFTR belongs to the ATP-binding cassette (ABC) superfamily. Mutations in CFTR cause the pulmonary disease, cystic fibrosis (CF).

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Human CFTR R Domain Antibody

1 Image
ICC/IF, IHC, IP, WB

CFTRinh 172

Voltage-independent, selective CFTR chloride channel blocker

GlyH 101

Reversible, voltage-dependent CFTR chloride channel blocker

KM 11060

Corrects F508del-CFTR trafficking

PG 01

CFTR potentiator; corrects F508del-CFTR conductance defect

PPQ 102

Potent, voltage-independent CFTR chloride channel inhibitor
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