VD2(Vitamin D2) ELISA Kit
Alternative Names: Ergocalciferol; Deltalin; Drisdol; Calcidol
Species: General
Assay Type: Competitive Inhibition
Sensitivity: 0.53 ng/mL
Standard: 100 ng/mL
Detection range: 1.57-100 ng/mL
Sample type: Serum, plasma and other biological fluids.
Assay length: 2h
Research Area: Metabolic pathway;Neuro science;Nutrition metabolism;Bone metabolism;
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with VD2 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to VD2. 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 VD2 in the samples is then determined by comparing the OD of the samples to the standard curve.
Price | 1.525,00 RON (preturile sunt fara TVA) |
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Description |
Alternative Names: Ergocalciferol; Deltalin; Drisdol; Calcidol Species: General Assay Type: Competitive Inhibition Sensitivity: 0.53 ng/mL Standard: 100 ng/mL Detection range: 1.57-100 ng/mL Sample type: Serum, plasma and other biological fluids. Assay length: 2h Research Area: Metabolic pathway;Neuro science;Nutrition metabolism;Bone metabolism; Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with VD2 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to VD2. 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 VD2 in the samples is then determined by comparing the OD of the samples to the standard curve. |