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Catalog
E025196
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species
Human
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GeneMCV
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SpecificityThis assay has high sensitivity and excellent specificity for detection of MCVAb. No significant cross-reactivity or interference between MCVAb and analogues was observed. NOTE: cross-reactivity detection between MCVAb and all the analogues, therefore, cross reaction may still exist in some cases.
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SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
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Sensitivity1.0 ng/mL.
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Intended UseHuman MCV ELISA Kit allows for the in vitro quantitative determination of MCV , concentrations in serum, Plasma , tissue homogenates and Cell culture supernates and Other biological fluids.
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StorageFor 5-7days:Store the whole kit at 4℃
For a Long time :Store the Substrate at 4℃, other reagent should store at -20℃.
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Product Categories/FamilyHuman ELISA Kit
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Product Description
specificalIntended Uses: This MCVAb ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human MCVAb. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
Principle of the Assay||MCVAb ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with Mutated Citrullinated Vimentin Antibody. Standards or samples are then added to the microtiter plate wells and MCVAb if present, will bind to the Mutated Citrullinated Vimentin Antibody pre-coated wells. In order to quantitatively determine the amount of MCVAb present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated MCVAb IgG added to each well to "sandwich" the MCVAb 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 MCVAb 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 MCVAb concentration in each sample is interpolated from this standard curve.
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