Bio-Connect

Horse sCD14 ELISA Kit

ORB1173547
Biorbyt
ReactivityEquine
Product group Assays
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Overview

  • Supplier
    Biorbyt
  • Product Name
    Horse sCD14 ELISA Kit
  • Delivery Days Customer
    10
  • Application Supplier Note
    standard: 20 ng/mL. Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Horse sCD14. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Horse sCD14. 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 Horse sCD14, 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 Horse sCD14 in the samples is then determined by comparing the OD of the samples to the standard curve
  • Applications
    ELISA
  • Applications Supplier
    ELISA
  • Assay Detection Range
    0.32-20 ng/mL
  • Assay Sensitivity
    0.238 ng/mL
  • Certification
    Research Use Only
  • Scientific Description
    The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to soluble cluster of differentiation 14(sCD14). Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to soluble cluster of differentiation 14(sCD14). 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 soluble cluster of differentiation 14(sCD14), 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 soluble cluster of differentiation 14(sCD14) in the samples is then determined by comparing the OD of the samples to the standard curve.
  • Reactivity
    Equine
  • UNSPSC
    41116158