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Catalog
E022004
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species
Human
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GeneLA
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Standard Curve
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Other Species
Human alpha-La ELISA KitHuman D La ELISA KitHuman D-LA ELISA KitHuman LA DR ELISA KitHuman LAC/LA ELISA KitHuman SS B/La ELISA KitHuman SS-B/La ELISA KitMouse alpha-La ELISA KitMouse D-LA ELISA KitMouse LA ELISA KitMouse LA-DR ELISA KitMouse LAC/LA ELISA KitMouse SS-B/La ELISA Kit
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SpecificityThis assay has high sensitivity and excellent specificity for detection of L-ARG. No significant cross-reactivity or interference between L-ARG and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between L-ARG 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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Sensitivity0.1 ug/mL.
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Intended UseHuman LA ELISA Kit allows for the in vitro quantitative determination of LA , 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 Description
specificalIntended Uses: This L-ARG ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human L-ARG. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
Principle of the Assay: L-ARG ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-L-ARG antibody and an L-ARG-HRP conjugate. The assay sample and buffer are incubated together with L-ARG-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the L-ARG concentration since L-ARG from samples and L-ARG-HRP conjugate compete for the anti-L-ARG antibody binding site. Since the number of sites is limited, as more sites are occupied by L-ARG from the sample, fewer sites are left to bind L-ARG-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The L-ARG concentration in each sample is interpolated from this standard curve.
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