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ELK6538-48T, Human OXM(Oxyntomodulin) ELISA Kit, 48T
2.142,00 RON
Human OXM(Oxyntomodulin) ELISA Kit
SKU
ELK6538-48T
Alternative Names: OXM
Species: Human
Assay Type: Competitive Inhibition
Sensitivity: 2.73 ng/mL
Standard: 500 ng/mL
Detection range: 7.82-500 ng/mL
Sample type: Serum, plasma and other biological fluids
Assay length: 2h
Research Area: Metabolic pathway;Endocrinology;Gastroenterology;Hormone metabolism;
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human OXM protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human OXM. 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 Human OXM in the samples is then determined by comparing the OD of the samples to the standard curve.
| Price | 1.800,00 RON (preturile sunt fara TVA) |
|---|---|
| Description |
Alternative Names: OXM Species: Human Assay Type: Competitive Inhibition Sensitivity: 2.73 ng/mL Standard: 500 ng/mL Detection range: 7.82-500 ng/mL Sample type: Serum, plasma and other biological fluids Assay length: 2h Research Area: Metabolic pathway;Endocrinology;Gastroenterology;Hormone metabolism; Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human OXM protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human OXM. 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 Human OXM in the samples is then determined by comparing the OD of the samples to the standard curve. |
