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CFTR (Phospho-Ser737) Polyclonal Antibody

Product Specifications

Background

Cystic fibrosis transmembrane conductance regulator (CFTR) Homo sapiens This gene encodes a member of the ATP-binding cassette (ABC) transporter superfamily. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White) . This protein is a member of the MRP subfamily that is involved in multi-drug resistance. The encoded protein functions as a chloride channel and controls the regulation of other transport pathways. Mutations in this gene are associated with the autosomal recessive disorders cystic fibrosis and congenital bilateral aplasia of the vas deferens. Alternatively spliced transcript variants have been described, many of which result from mutations in this gene. [provided by RefSeq, Jul 2008]

Product Name Alternative

Cystic fibrosis transmembrane conductance regulator (CFTR; ATP-binding cassette sub-family C member 7; Channel conductance-controlling ATPase; EC 3.6.3.49; cAMP-dependent chloride channel)

Gene ID

1080

Swiss Prot

P13569

Cross Reactivity

Human; Mouse; Rat

Clonality

Polyclonal

Source

Rabbit

Applications

IHC-p; IF (paraffin section) ; WB

Dilution

IHC-p 1:50-200, WB 1:500-2000

Buffer

Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

Molecular Weight

166

Storage Conditions

-20°C/1 year

Protein Weight

166

Available Sizes

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