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Alternative name
Serine/threonine-protein kinase receptor R3 ELISA KIT; Activin receptor-like kinase 1 ELISA KIT; ALK-1 ELISA KIT; TGF-B superfamily receptor type I ELISA KIT; TSR-IACVRL1 ELISA KIT; ACVRLK1 ELISA KIT; ALK1 ELISA KIT; SKR3 ELISA KIT; ALK-1 ELISA KIT; TSR-I ELISA KIT
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Catalog
E000537
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species
Human
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GeneALK1
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Standard Curve
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Other Species
Mouse ALK1 ELISA Kit
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SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
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Intended UseHuman ALK1 ELISA Kit allows for the in vitro quantitative determination of ALK1 , concentrations in serum, Plasma , tissue homogenates and Cell culture supernates and Other biological fluids.
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StorageFor 5-7days:Store the whole kit at 4℃
For a Long time :Store the Substrate at 4℃, other reagent should store at -20℃.
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Product Categories/FamilySignal Transduction
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Product Description
specificalFor Samples: Serum, plasma, cell culture supernatants, body fluid and tissue homogenate
Intended Uses: This ALK1 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human ALK1. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
Principle of the Assay: ALK1 ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for ALK1. Standards or samples are then added to the microtiter plate wells and ALK1 if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of ALK1 present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for ALK1 are added to each well to "sandwich" the ALK1 immobilized on the plate. The microtiter plate undergoes incubation, and then the wells are thoroughly washed to remove all unbound components. Next, substrate solutions are added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period. Only those wells that contain ALK1 and enzyme-conjugated antibody will exhibit a change in color. The enzyme-substrate reaction is terminated by addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The ALK1 concentration in each sample is interpolated from this standard curve.
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