Human GF(Glycosylated Ferritin) ELISA Kit
Alternative Names: Glycosylated Ferritin; GF
Species: Human
Assay Type: Competitive Inhibition
Sensitivity: 10.19 nmol/mL
Standard: 2000 nmol/mL
Detection range: 31.25-2000 nmol/mL
Sample type: serum, plasma
Assay length: 2h
Research Area: Diabetes
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human GF protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human GF. 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 GF in the samples is then determined by comparing the OD of the samples to the standard curve.
Price | 2.490,00 RON (preturile sunt fara TVA) |
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Description |
Alternative Names: Glycosylated Ferritin; GF Species: Human Assay Type: Competitive Inhibition Sensitivity: 10.19 nmol/mL Standard: 2000 nmol/mL Detection range: 31.25-2000 nmol/mL Sample type: serum, plasma Assay length: 2h Research Area: Diabetes Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human GF protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human GF. 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 GF in the samples is then determined by comparing the OD of the samples to the standard curve. |