SpecificityThis assay has high sensitivity and excellent specificity for detection of GLY. No significant cross-reactivity or interference between GLY and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between GLY and all the analogues, therefore, cross reaction may still exist in some cases.
Intended UseHuman GAGs ELISA Kit allows for the in vitro quantitative determination of GAGs , concentrations in serum, Plasma , tissue homogenates and Cell culture supernates and Other biological fluids.
StorageFor 5-7days:Store the whole kit at 4℃
For a Long time :Store the Substrate at 4℃, other reagent should store at -20℃.
Product Categories/FamilyCell Biology
Product Description specificalIntended Uses: This GLY ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human GLY. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
Principle of the Assay||GLY ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for GLY. Standards or samples are then added to the microtiter plate wells and GLY if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of GLY present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for GLY are added to each well to "sandwich" the GLY immobilized on the plate. The microtiter plate undergoes incubation, and then the wells are thoroughly washed to remove all unbound components. Next, substrate solutions are added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period. Only those wells that contain GLY and enzyme-conjugated antibody will exhibit a change in color. The enzyme-substrate reaction is terminated by addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The GLY concentration in each sample is interpolated from this standard curve.