Human sFLT(Soluble Fms-Like Tyrosine Kinase Receptor 1) ELISA Kit

Biorbyt

Human sFLT(Soluble Fms-Like Tyrosine Kinase Receptor 1) ELISA Kit

10

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 sFLT. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human sFLT. 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 sFLT, 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 sFLT in the samples is then determined by comparing the OD of the samples to the standard curve

0.16-10 ng/mL

0.059 ng/mL

Research Use Only

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 Fms-Like Tyrosine Kinase Receptor 1(sFLT). Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Soluble Fms-Like Tyrosine Kinase Receptor 1(sFLT). 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 Fms-Like Tyrosine Kinase Receptor 1(sFLT), 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 Fms-Like Tyrosine Kinase Receptor 1(sFLT) in the samples is then determined by comparing the OD of the samples to the standard curve.

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