1,5-AG(1,5-Anhydroglucitol) ELISA Kit
Alternative Names: LycoMark; 1-Deoxy-D-glucose; 1-Deoxy-D-glucopyranose; 1,5-Anhydro-D-glucitol; 1,5-Anhydrosorbitol; Aceritol; Polygalytol
Species: General
Assay Type: Competitive Inhibition
Sensitivity: 0.6 µg/mL
Standard: 150 µg/mL
Detection range: 2.35-150 µg/mL
Sample type: serum, plasma and other biological fluids
Assay length: 2h
Research Area: Enzyme & Kinase;Metabolic pathway;Endocrinology;Nutrition metabolism;
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with 1,5-AG protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to 1,5-AG. 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 1,5-AG 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: LycoMark; 1-Deoxy-D-glucose; 1-Deoxy-D-glucopyranose; 1,5-Anhydro-D-glucitol; 1,5-Anhydrosorbitol; Aceritol; Polygalytol Species: General Assay Type: Competitive Inhibition Sensitivity: 0.6 µg/mL Standard: 150 µg/mL Detection range: 2.35-150 µg/mL Sample type: serum, plasma and other biological fluids Assay length: 2h Research Area: Enzyme & Kinase;Metabolic pathway;Endocrinology;Nutrition metabolism; Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with 1,5-AG protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to 1,5-AG. 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 1,5-AG in the samples is then determined by comparing the OD of the samples to the standard curve. |