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Alternative name
Interleukin-33 ELISA KIT; Interleukin-1 family member 11 ELISA KIT; IL-1F11 ELISA KIT; Nuclear factor from high endothelial venulesIL33 ELISA KIT; C9orf26 ELISA KIT; IL1F11 ELISA KIT; NFHEV ELISA KIT
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Catalog
E057357
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species
Mouse
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GeneIL-33/ST2
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SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
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Intended UseMouse IL-33/ST2 ELISA Kit allows for the in vitro quantitative determination of IL-33/ST2 , 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/FamilyMouse ELISA Kit
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Product Description
specificalIntended Uses: This IL-33/ST2 ELISA kit is intended Laboratory for research use only and is not for use in diagnostic or therapeutic procedures.The Stop Solution changes the color from blue to yellow and the intensity of the color is measured at 450 nm using a spectrophotometer. In order to measure the concentration of IL-33/ST2in the sample, this IL-33/ST2ELISA Kit includes a set of calibration standards. The calibration standards are assayed at the same time as the samples and allow the operator to produce a standard curve of Optical Density versus IL-33/ST2concentration. The concentration of IL-33/ST2in the samples is then determined by comparing the O.D. of the samples to the standard curve.
Principle of the Assay: This IL-33/ST2enzyme linked immunosorbent assay applies a technique called a quantitative sandwich immunoassay. The microtiter plate provided in this kit has been pre-coated with a monoclonal antibody specific for IL-33/ST2. Standards or samples are then added to the microtiter plate wells and IL-33/ST2if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of IL-33/ST2present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for IL-33/ST2are added to each well to "sandwich" the IL-33/ST2immobilized on the plate. The microtiter plate undergoes incubation, and then the wells are thoroughly washed to remove all unbound components. Next, A and B substrate solution is added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period.Only those wells that contain IL-33/ST2and enzyme-conjugated antibody will exhibit a change in colour. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the colour change is measured spectrophotometrically at a wavelength of 450 nm.
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