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ELK Biotechnology
SKU:ELK9036
Human suPAR(soluble urokinase-type plasminogen activator receptor) ELISA Kit
Human suPAR(soluble urokinase-type plasminogen activator receptor) ELISA Kit
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Alternative Names: CD87; PLAUR; PLAU-R; U-PAR; URKR; Monocyte Activation Antigen Mo3
Assay Type: Sandwich
Sensitivity: 0.056 ng/mL
standard: 10 ng/mL
Detection range: 0.16-10 ng/mL
Sample type: Serum, plasma and other biological fluids.
Assay length: 3.5h
Research Area: Tumor immunity;
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 suPAR. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human suPAR. 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 suPAR, 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 suPAR in the samples is then determined by comparing the OD of the samples to the standard curve.
Assay Type: Sandwich
Sensitivity: 0.056 ng/mL
standard: 10 ng/mL
Detection range: 0.16-10 ng/mL
Sample type: Serum, plasma and other biological fluids.
Assay length: 3.5h
Research Area: Tumor immunity;
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 suPAR. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human suPAR. 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 suPAR, 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 suPAR in the samples is then determined by comparing the OD of the samples to the standard curve.
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