Human IL 12p35 ELISA Kit

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  • Alternative name

    Interleukin 12 polypeptide 35 ELISA KIT; Interleukin 12 polypeptide 35IL12 ELISA KIT;

  • Catalog
  • species
  • GeneIL 12p35
  • Standard CurveHuman IL 12p35 ELISA Kit
  • Other Species Mouse IL-12p35 ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of IL-12p35. No significant cross-reactivity or interference between IL-12p35 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between IL-12p35 and all the analogues, therefore, cross reaction may still exist in some cases.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity1.0 pg/mL.
  • Intended UseHuman IL 12p35 ELISA Kit allows for the in vitro quantitative determination of IL 12p35 , 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 Categories/FamilyImmunology
  • Product Description
    Intended Uses||This IL-12p35 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human IL-12p35. This ELISA kit for research use only, not for therapeutic or diagnostic applications! Principle of the Assay: IL-12p35 ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-IL-12p35 antibody and an IL-12p35-HRP conjugate. The assay sample and buffer are incubated together with IL-12p35-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-12p35 concentration since IL-12p35 from samples and IL-12p35-HRP conjugate compete for the anti-IL-12p35 antibody binding site. Since the number of sites is limited, as more sites are occupied by IL-12p35 from the sample, fewer sites are left to bind IL-12p35-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The IL-12p35 concentration in each sample is interpolated from this standard curve.

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