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Alternative name
Arachidonate 5-lipoxygenase ELISA KIT; ALOX5 ELISA KIT; LOG5 ELISA KIT; 5-LO ELISA KIT; 5-lipoxygenase ELISA KIT
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Catalog
E003528
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species
Human
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GeneALOX 5
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Standard Curve
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Other Species
Human ALOX-5 ELISA KitMouse ALOX-5 ELISA Kit
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SpecificityThis assay has high sensitivity and excellent specificity for detection of ALOX5. No significant cross-reactivity or interference between ALOX5 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between ALOX5 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 ng/mL.
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Intended UseHuman ALOX 5 ELISA Kit allows for the in vitro quantitative determination of ALOX 5 , 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 ALOX5 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human ALOX5. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
Principle of the Assay||ALOX5 ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for ALOX5. Standards or samples are then added to the microtiter plate wells and ALOX5 if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of ALOX5 present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for ALOX5 are added to each well to "sandwich" the ALOX5 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 ALOX5 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 ALOX5 concentration in each sample is interpolated from this standard curve.
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