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Human TU3A ELISA Kit

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  • Alternative name

    Protein FAM107A ELISA KIT; Down-regulated in renal cell carcinoma 1 ELISA KIT; Protein TU3AFAM107A ELISA KIT; DRR1 ELISA KIT; TU3A ELISA KIT
  • Catalog
    E039761
  • species
    Human
  • GeneTU3A
  • SpecificityThis kit recognizes natural and recombinant Human TU3A. No significant cross-reactivity or interference between Human TU3A and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity46.875pg/mL
  • Intended UseHuman TU3A ELISA Kit allows for the in vitro quantitative determination of TU3A , 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    Intended Uses: This ELISA kit applies to the in vitro quantitative determination of Human TU3A concentrations in serum, plasma and other biological fluids. Principle of the Assay||This ELISA kit uses Sandwich-ELISA as the method. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to TU3A. Standards or samples are added to the appropriate micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for TU3A and Avidin-Horseradish Peroxidase (HRP) conjugate is added to each micro plate well successively and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain TU3A, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm +/- 2 nm. The OD value is proportional to the concentration of TU3A. You can calculate the concentration of TU3A in the samples by comparing the OD of the samples to the standard curve.



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