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Alternative name
Proteinase-activated receptor 1 ELISA KIT; Coagulation factor II receptor ELISA KIT; Thrombin receptorF2R ELISA KIT; CF2R ELISA KIT; PAR1 ELISA KIT; TR ELISA KIT; PAR-1 ELISA KIT
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Catalog
E064960
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species
Mouse
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GenePAR1
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SpecificityThis assay has high sensitivity and excellent specificity for detection of PAR1. No significant cross-reactivity or interference between PAR1 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between PAR1 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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Sensitivity0.1 ng/mL.
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Intended UseMouse PAR1 ELISA Kit allows for the in vitro quantitative determination of PAR1 , 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
specificalPrinciple of the assay: PAR1 ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-PAR1 antibody and an PAR1-HRP conjugate. The assay sample and buffer are incubated together with PAR1-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the PAR1 concentration since PAR1 from samples and PAR1-HRP conjugate compete for the anti-PAR1 antibody binding site. Since the number of sites is limited, as more sites are occupied by PAR1 from the sample, fewer sites are left to bind PAR1-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The PAR1 concentration in each sample is interpolated from this standard curve.
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