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ELK Biotechnology
SKU:ELK0424
SA(Sialic Acid) ELISA Kit
SA(Sialic Acid) ELISA Kit
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$558.00 USD
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Alternative Names: SA
Assay Type: Competitive Inhibition
Sensitivity: 25.5 µg/mL
standard: 5000 µg/mL
Detection range: 78.13-5000 µg/mL
Sample type: Serum, plasma, tissue homogenates and other biological fluids.
Assay length: 2.5h
Research Area: Signal transduction;Tumor immunity;Hepatology;
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with SA protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to SA. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 SA in the samples is then determined by comparing the OD of the samples to the standard curve.
Assay Type: Competitive Inhibition
Sensitivity: 25.5 µg/mL
standard: 5000 µg/mL
Detection range: 78.13-5000 µg/mL
Sample type: Serum, plasma, tissue homogenates and other biological fluids.
Assay length: 2.5h
Research Area: Signal transduction;Tumor immunity;Hepatology;
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with SA protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to SA. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 SA in the samples is then determined by comparing the OD of the samples to the standard curve.
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