Human alpha-CTx ELISA Kit

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  • Catalog
    E001614
  • species
    Human
  • Genealpha-CTx
  • Other Species Mouse alpha-CTx ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Human alpha-CTx. No significant cross-reactivity or interference between Human alpha-CTx and analogues was observed. Note: Limited by current skills and knowledge, it is impossible for us to complete the cross- reactivity detection between Human alpha-CTx and all the analogues, therefore, cross reaction may still exist.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity56.25pg/mL
  • Intended UseHuman alpha-CTx ELISA Kit allows for the in vitro quantitative determination of alpha-CTx , 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 Description
    specifical
    Description: The kit is a competitive enzyme immunoassay for in vitro quantitative measurement of alpha-CTx in human serum, plasma and other biological fluids Principle of the Assay: This ELISA kit uses Competitive-ELISA as the method. The microtiter plate provided in this kit has been pre-coated with Human alpha-CTx. During the reaction, Human alpha-CTx in the sample or standard competes with a fixed amount of Human alpha-CTx on the solid phase supporter for sites on the Biotinylated Detection Ab specific to Human alpha-CTx. Excess conjugate and unbound sample or standard are washed from the plate, and Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm +/- 2 nm. The concentration of Human alpha-CTx in the samples is then determined by comparing the O.D. of the samples to the standard curve.


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