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Catalog
E006751
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species
Human
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                                    GeneCAR 
                                
                             
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                                    SpecificityThis assay has high sensitivity and excellent specificity for detection of CAR. No significant cross-reactivity or interference between CAR and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between CAR 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 ng/mL.
                                
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                                Intended UseHuman CAR ELISA Kit allows for the in vitro quantitative determination of CAR  , 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: CAR ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-CAR antibody and an CAR-HRP conjugate. The assay sample and buffer are incubated together with CAR-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 CAR concentration since CAR from samples and CAR-HRP conjugate compete for the anti-CAR antibody binding site. Since the number of sites is limited, as more sites are occupied by CAR from the sample, fewer sites are left to bind CAR-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The CAR concentration in each sample is interpolated from this standard curve.
                                 
                                                                                                                                                                                                    
                                                        
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