This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Human FSH. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Human FSH are added to the micro ELISA plate wells. Human FSH in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Human FSH.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Human FSH. The concentration of Human FSH in the samples is then determined by comparing the OD of the samples to the standard curve.
This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Human GAL3. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Human GAL3 are added to the micro ELISA plate wells. Human GAL3 in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Human GAL3.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Human GAL3. The concentration of Human GAL3 in the samples is then determined by comparing the OD of the samples to the standard curve.
This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Human GDF15. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Human GDF15 are added to the micro ELISA plate wells. Human GDF15 in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Human GDF15.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Human GDF15. The concentration of Human GDF15 in the samples is then determined by comparing the OD of the samples to the standard curve.
This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Human HCG. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Human HCG are added to the micro ELISA plate wells. Human HCG in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Human HCG.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Human HCG. The concentration of Human HCG in the samples is then determined by comparing the OD of the samples to the standard curve.
This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to HO1 . Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for HO1 and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain HO1 , biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 19 nm. The OD value is proportional to the concentration of HO1 . You can calculate the concentration of HO1 in the samples by comparing the OD of the samples to the standard curve.
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