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CFTR antibody

Antigen

CFTR

Clonality Polyclonal
Host
Alternatives

Rabbit

Reactivity
Alternatives

Human, Rat (Rattus)

Application
Alternatives Western Blotting (WB), Immunohistochemistry (IHC)
Catalog no. ABIN459908
Quantity 100µg  (1 mg/ml)  (Variants)
Price 743.71 $   Plus shipping costs $35.00
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Availability Ships within 7 to 10 Business Days

Additional Information

Format Liquid
Description CFTR, for cystic fibrosis transmembrane conductance regulator, is a cyclic adenosine monophosphate (cAMP)-regulated chloride channel protein. CFTR belongs to the MDR subfamily within the ATP-binding transport protein family. It has two transmembrane domains (TMDs), two nucleotide binding domains (NBDs) and one regulatory domain. Mutations of CFTR are associated with cystic fibrosis (CF), a disease characterized by chronic bronchopulmonary disease, elevated sweat electrolytes and insufficient pancreatic function. CFTR mutations can also result in congenital bilateral absence of vas deferens (CBAVD), a form of male sterility that a majority of male CF patients exhibit.
Synonyms: CFTR, ABC35, ABCC7, CBAVD, CF, CFTR/MRP, DJ760C5.1, MRP7, TNR-CFTR
Specificity CFTR (E733) pAb detects endogenous levels of CFTR protein.
Molecular Weight 168 kDa

Application Details

Application Notes IHC: 1:50-1:200 WB: 1:500-1:1000
Concentration 1 mg/ml
Purity > 95% (by SDS-PAGE).
Purification The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Buffer 1 mg/ml in Phosphate buffered saline (PBS) with 0.05% sodium azide, approx. pH 7.2.
Storage Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
Restrictions For Research Use only