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Human HSP 90 ELISA Kit

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  • Alternative name

    Heat shock protein 90 ELISA KIT; 65 kDa IgE-binding protein ELISA KIT; Heat shock protein hsp1 ELISA KIT; Allergen: Asp f 12hsp90 ELISA KIT; hsp1 ELISA KIT; AFUA_5G04170 ELISA KIT
  • Catalog
    E018015
  • species
    Human
  • GeneHSP 90
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of HSP-90. No significant cross-reactivity or interference between HSP-90 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between HSP-90 and all the analogues, therefore, cross reaction may still exist in some cases.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity0.1 ng/mL.
  • Intended UseHuman HSP 90 ELISA Kit allows for the in vitro quantitative determination of HSP 90 , concentrations in serum, Plasma , tissue homogenates and Cell culture supernates and Other biological fluids.
  • StorageFor 5-7days:Store the whole kit at 4℃
    For a Long time :Store the Substrate at 4℃, other reagent should store at -20℃.
  • Product Categories/FamilySignal Transduction
  • Product Description
    specifical    Principle of the assay: HSP-90 ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for HSP-90. Standards or samples are then added to the microtiter plate wells and HSP-90 if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of HSP-90 present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for HSP-90 are added to each well to "sandwich" the HSP-90 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 HSP-90 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 HSP-90 concentration in each sample is interpolated from this standard curve.



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