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Horse BNIP3L(Leucine rich repeat and Ig domain containing 1) ELISA Kit

ORB1146863
Biorbyt
ReactivityEquine
Product group Assays
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Overview

  • Supplier
    Biorbyt
  • Product Name
    Horse BNIP3L(Leucine rich repeat and Ig domain containing 1) ELISA Kit
  • Delivery Days Customer
    10
  • Application Supplier Note
    standard: 10 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 Lingo1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Horse Lingo1. 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 Lingo1, 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 Lingo1 in the samples is then determined by comparing the OD of the samples to the standard curve
  • Assay Detection Range
    0.16-10 ng/mL
  • Assay Sensitivity
    0.097 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 Horse Lingo1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Horse Lingo1. 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 Lingo1, 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 Lingo1 in the samples is then determined by comparing the OD of the samples to the standard curve.
  • Reactivity
    Equine
  • UNSPSC
    41116158