Product: AP10443PU-NABCC7 / CFTR antibody
Quantity: 0.1 mg
Synonyms: ATP-binding cassette transporter sub-family C member 7, Channel conductance-controlling ATPase, Cystic fibrosis transmembrane conductance regulator, cAMP-dependent chloride channel
Presentation: Purified
Clonality: Polyclonal
Host: Rabbit
Isotype:
CAS NO: 35457-80-8 Product: Midecamycin
Shipping to: Worldwide
Immunogen: Synthetic peptide derived from Cter domain of human CFTR protein.GeneID:1080
Application: ELISA: 1/2000-1/32000. Western Blot: 1/500-1/1000.Immunofluorescence. Immunoprecipitation.
Background: Cystic Fibrosis (CF) is a common lethal genetic disease characterized by chronic bronchopulmonary disease, elevated sweat electrolytes and insufficient pancreatic function. CF is caused by mutations of the CFTR gene, which encodes the cystic fibrosis tran
Concentration: 1 mg/ml
Storage: Store lyophilized at 2-8°C for 6 months or at -20°C long term.After reconstitution store the antibody undiluted at 2-8°C for one monthor (in aliquots) at -20°C long term.Avoid repeated freezing and thawing.Shelf life: one year from despatch.
Buffer System: 0.1M Tris 0.1M Glycine, 2% Sucrose
Preservatives: None
State: Lyophilized purified antibodyPurified
Specifictiy: Reacts with Human 168 kDa CFTR.
