Interleukin-36 beta ELISA KIT; FIL1 eta ELISA KIT; Interleukin-1 eta ELISA KIT; IL-1 eta ELISA KIT; Interleukin-1 family member 8 ELISA KIT; IL-1F8 ELISA KIT; Interleukin-1 homolog 2 ELISA KIT; IL-1H2IL36B ELISA KIT; IL1F8 ELISA KIT; IL1H2 ELISA KIT; IL-1 eta ELISA KIT; IL-1F8 ELISA KIT; IL-1H2 ELISA KIT
GeneIL 36 beta/ IL 1F8/FIL 1h/IL 1H2
SpecificityThis assay has high sensitivity and excellent specificity for detection of IL-36beta. No significant cross-reactivity or interference between IL-36beta and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between IL-36beta and all the analogues, therefore, cross reaction may still exist in some cases.
Intended UseHuman IL 36 beta/ IL 1F8/FIL 1h/IL 1H2 ELISA Kit allows for the in vitro quantitative determination of IL 36 beta/ IL 1F8/FIL 1h/IL 1H2 , 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 Description specificalPrinciple of the Assay: IL-36beta ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-IL-36beta antibody and an IL-36beta-HRP conjugate. The assay sample and buffer are incubated together with IL-36beta-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 IL-36beta concentration since IL-36beta from samples and IL-36beta-HRP conjugate compete for the anti-IL-36beta antibody binding site. Since the number of sites is limited, as more sites are occupied by IL-36beta from the sample, fewer sites are left to bind IL-36beta-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The IL-36beta concentration in each sample is interpolated from this standard curve.
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