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Human CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) ELISA Kit

Human CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) ELISA Kit

The Human (CFTR) Cystic Fibrosis Transmembrane Conductance Regulator ELISA Kit measures Cystic Fibrosis Transmembrane Conductance Regulator in samples. The plate has been pre-coated with Human CFTR antibody. CFTR present in the sample is added and binds to antibodies coated on the wells. And then biotinylated Human CFTR Antibody is added and binds to CFTR in the sample. Then Streptavidin-HRP is added and binds to the Biotinylated CFTR antibody. After incubation unbound Streptavidin-HRP is washed away during a washing step. Substrate solution is then added and color develops in proportion to the amount of Human CFTR. The reaction is terminated by addition of acidic stop solution and absorbance is measured at 450 nm.

Catalog No: E4110hu
Regular price $595.00 USD
Regular price $458.00 USD Sale price $595.00 USD
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2.5 weeks
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Product Details

Species Reactivity Human
Sensitivity 9.28 ng/L
Detection Range 20-3800 ng/L
Sample Type Serum, plasma, cell culture supernates
Incubation(s) 1.5 hour(s)
Research Areas Signal Transduction
Background Epithelial ion Channel that plays an important role in the regulation of epithelial ion and water transport and fluid homeostasis (PubMed: 26823428). Mediates the transport of chloride ions across the cell membrane (PubMed: 10792060, PubMed: 11524016, PubMed: 11707463, PubMed: 12519745, PubMed: 15010471, PubMed: 12588899, PubMed: 17036051, PubMed: 19398555, PubMed: 19621064, PubMed: 22178883, PubMed: 25330774, PubMed: 1712898, PubMed: 8910473, PubMed: 9804160, PubMed: 12529365, PubMed: 17182731, PubMed: 26846474, PubMed: 28087700). Channel activity is coupled to ATP hydrolysis (PubMed: 8910473). The ion Channel is also permeable to HCO(3-); selectivity depends on the extracellular chloride concentration (PubMed: 15010471, PubMed: 19019741). Exerts its function also by modulating the activity of other ion Channels and transporters (PubMed: 12403779, PubMed: 22178883, PubMed: 22121115, PubMed: 27941075). Plays an important role in airway fluid homeostasis (PubMed: 16645176, PubMed: 19621064, PubMed: 26823428). Contributes to the regulation of the pH and the ion content of the airway surface fluid layer and thereby plays an important role in defense against pathogens (PubMed: 14668433, PubMed: 16645176, PubMed: 26823428). Modulates the activity of the epithelial sodium Channel (ENaC) complex, in part by regulating the cell surface expression of the ENaC complex (PubMed: 17434346, PubMed: 27941075, PubMed: 17182731). Inhibits the activity of the ENaC Channel containing subunits SCNN1A, SCNN1B and SCNN1G (PubMed: 17182731). Inhibits the activity of the ENaC Channel containing subunits SCNN1D, SCNN1B and SCNN1G, but not of the ENaC Channel containing subunits SCNN1A, SCNN1B and SCNN1G (PubMed: 27941075). May regulate bicarbonate secretion and salvage in epithelial cells by regulating the transporter SLC4A7 (PubMed: 12403779). Can inhibit the chloride Channel activity of ANO1 (PubMed: 22178883). Plays a role in the chloride and bicarbonate homeostasis during sperm epididymal maturation and capacitation (PubMed: 19923167, PubMed: 27714810). Source: UniProt Consortium (2025)
Shipping Condition Shipped on cold gel packs.
Storage Condition and Shelf Life 2-8C
Analyte Cystic Fibrosis Transmembrane Conductance Regulator
Regulatory Status For Research Use Only
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