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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). Specifically, deletion of phenyalanine at position 508 (DeltaF508-CFTR) results in a f...

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Reactivity: Human, Mouse, Rat, Chicken, Golden Syrian Hamster
Details: Mouse IgM Monoclonal Clone #CF3
Applications: IHC, WB, B/N, Flow, ICC/IF, + 1 More
Immunocytochemistry/ Immunofluorescence: CFTR Antibody (CF3) [NB300-511]
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