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Human BAD(Bcl2 antagonist of cell death) ELISA Kit

ORB1146801
Biorbyt
ReactivityHuman
Product group Assays
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Overview

  • Supplier
    Biorbyt
  • Product Name
    Human BAD(Bcl2 antagonist of cell death) 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 Human BAD. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human BAD. 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 Human BAD, 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 Human BAD 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
    0.056 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 Bcl2 antagonist of cell death(BAD). Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Bcl2 antagonist of cell death(BAD). 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 Bcl2 antagonist of cell death(BAD), 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 Bcl2 antagonist of cell death(BAD) in the samples is then determined by comparing the OD of the samples to the standard curve.
  • Reactivity
    Human
  • UNSPSC
    41116158

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