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ELK Biotechnology
SKU:ELK10958
Horse a2M(Alpha-2-Macroglobulin) ELISA Kit
Horse a2M(Alpha-2-Macroglobulin) ELISA Kit
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$476.00 USD
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Alternative Names: α2MG; α2Mg; CPAMD5; C3 and PZP-like alpha-2-macroglobulin domain-containing protein 5
Assay Type: Sandwich
Sensitivity: 2.16 µg/mL
standard: 500 µg/mL
Detection range: 7.82-500 µg/mL
Sample type: serum, plasma, urine and other biological fluids
Assay length: 3.5h
Research Area: Tumor immunity;Infection immunity;Hematology;
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 Horse a2M. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Horse a2M. 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 Horse a2M, 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 Horse a2M in the samples is then determined by comparing the OD of the samples to the standard curve.
Assay Type: Sandwich
Sensitivity: 2.16 µg/mL
standard: 500 µg/mL
Detection range: 7.82-500 µg/mL
Sample type: serum, plasma, urine and other biological fluids
Assay length: 3.5h
Research Area: Tumor immunity;Infection immunity;Hematology;
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 Horse a2M. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Horse a2M. 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 Horse a2M, 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 Horse a2M in the samples is then determined by comparing the OD of the samples to the standard curve.
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