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ELK Biotechnology
SKU:ELK4074
Human SI(Sucrase Isomaltase) ELISA Kit
Human SI(Sucrase Isomaltase) ELISA Kit
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Alternative Names: Oligosaccharide Alpha-1;6-Glucosidase
Assay Type: Sandwich
Sensitivity: 0.108 ng/mL
standard: 20 ng/mL
Detection range: 0.32-20 ng/mL
Sample type: Tissue homogenates and other biological fluids.
Assay length: 3.5h
Research Area: Enzyme & Kinase;
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 SI. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human SI. 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 SI, 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 SI in the samples is then determined by comparing the OD of the samples to the standard curve.
UniProt ID: P14410
Assay Type: Sandwich
Sensitivity: 0.108 ng/mL
standard: 20 ng/mL
Detection range: 0.32-20 ng/mL
Sample type: Tissue homogenates and other biological fluids.
Assay length: 3.5h
Research Area: Enzyme & Kinase;
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 SI. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human SI. 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 SI, 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 SI in the samples is then determined by comparing the OD of the samples to the standard curve.
UniProt ID: P14410
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