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Zebrafish GR(Glutathione Reductase) ELISA Kit

ORB1088180
Biorbyt
Product group Assays
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Overview

  • Supplier
    Biorbyt
  • Product Name
    Zebrafish GR(Glutathione Reductase) ELISA Kit
  • Delivery Days Customer
    10
  • Application Supplier Note
    standard: 5000 pg/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 Zebrafish GR. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Zebrafish GR. 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 Zebrafish GR, 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 Zebrafish GR in the samples is then determined by comparing the OD of the samples to the standard curve
  • Assay Detection Range
    78.13-5000 pg/mL
  • Assay Sensitivity
    37 pg/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 Glutathione Reductase(GR). Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Glutathione Reductase(GR). 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 Glutathione Reductase(GR), 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 Glutathione Reductase(GR) in the samples is then determined by comparing the OD of the samples to the standard curve.
  • UNSPSC
    41116158