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Alternative name
Peroxisome proliferator-activated receptor alpha ELISA KIT; Nuclear receptor subfamily 1 group C member 1PPARA ELISA KIT; NR1C1 ELISA KIT; PPAR ELISA KIT; PPAR-alpha ELISA KIT
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Catalog
E063335
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species
Mouse
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GenePPARalpha
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Standard Curve
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Other Species
Human PPARalpha ELISA Kit
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SpecificityThis assay has high sensitivity and excellent specificity for detection of PPARalpha. No significant cross-reactivity or interference between PPARalpha and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between PPARalpha and all the analogues, therefore, cross reaction may still exist in some cases.
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SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
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Sensitivity1.0 pg/mL.
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Intended UseMouse PPARalpha ELISA Kit allows for the in vitro quantitative determination of PPARalpha , 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 Description
specificalPrinciple of the assay: PPARalpha ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for PPARalpha. Standards or samples are then added to the microtiter plate wells and PPARalpha if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of PPARalpha present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for PPARalpha are added to each well to "sandwich" the PPARalpha 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 PPARalpha 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 PPARalpha concentration in each sample is interpolated from this standard curve.
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