Human PTPRZ ELISA Kit

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  • Alternative name

    Receptor-type tyrosine-protein phosphatase zeta ELISA KIT; Protein-tyrosine phosphatase receptor type Z polypeptide 1 ELISA KIT; Protein-tyrosine phosphatase receptor type Z polypeptide 2 ELISA KIT; R-PTP-zeta-2PTPRZ1 ELISA KIT; HTPZP2 ELISA KIT; PTPRZ ELISA KIT; PTPRZ2 ELISA KIT; PTPZ ELISA KIT; R-PTP-zeta ELISA KIT

  • Catalog
    E031865
  • species
    Human
  • GenePTPRZ
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of PTPRZ. No significant cross-reactivity or interference between PTPRZ and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity0.054ng/mL.
  • Intended UseHuman PTPRZ ELISA Kit allows for the in vitro quantitative determination of PTPRZ , 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: The kit is a sandwich enzyme immunoassay for in vitro quantitative measurement of PTPRZ in human tissue homogenates, cell lysates and other biological fluids. Principle of the Assay||The microtiter plate provided in this kit has been pre-coated with an antibody specific to PTPRZ. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to PTPRZ. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain PTPRZ, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm +/- 10nm. The concentration of PTPRZ in the samples is then determined by comparing the O.D. of the samples to the standard curve.



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