CFTR polyclonal, anti-human, mouse, rat, monkey, xenopus

Protein Family: Receptors and Channels, Transporters

Pathway and Disease: Membrane Transport, Metabolic Disorders

Description:
Cystic fibrosis transmembrane conductance regulator (CFTR), a ABC transporter, is involved in the transport of chloride ions and regulates bicarbonate secretion in epithelial cells by regulating the SLC4A7 transporter. CFTR is localized in aggresome bodies when proteasome's degradative capacity is exceeded and lysosomal degradation is engaged via autophagy. Defects in CFTR are the cause of cystic fibrosis.

Alternate Names: Cystic fibrosis transmembrane conductance regulator, CFTR, cAMP-dependent chloride channel, ATP-binding cassette transporter sub-family C member 7, ABCC7

Application Notes: E: 1:500-1:1,000; WB: 1:100-1:500

Accession No.: P13569, NP_000483

Antigen: KLH-conjugated synthetic peptide encompassing a sequence within the N-term region of human CFTR.

Format: Each vial contains 0.1 mg IgG in 0.1 ml (1 mg/ml) of PBS pH7.4 with 0.09% sodium azide. Antibody was purified by Protein-G affinity chromatography.

Storage:
Store at -20°C. Minimize freeze-thaw cycles. Product is guaranteed one year from the date of shipment.