Human ELN Ab ELISA Kit

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  • Alternative name

    Elastin ELISA KIT; TropoelastinELN ELISA KIT;

  • Catalog
    E012886
  • species
    Human
  • GeneELN Ab
  • Standard CurveHuman ELN Ab ELISA Kit
  • Other Species Mouse ELN Ab ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of ELN Ab. No significant cross-reactivity or interference between ELN Ab and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between ELN Ab 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 ng/mL
  • Intended UseHuman ELN Ab ELISA Kit allows for the in vitro quantitative determination of ELN Ab , 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/FamilyCell Biology
  • Product Description
    specifical
    Intended Uses: This ELN Ab ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human ELN Ab. This ELISA kit for research use only, not for therapeutic or diagnostic applications! Principle of the Assay: ELN Ab ELISA kit applies the competitive enzyme immunoassay technique utilizing FLN antigen and an ELN Ab-HRP conjugate. The assay sample and buffer are incubated together with ELN Ab-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 ELN Ab concentration since ELN Ab from samples and ELN Ab-HRP conjugate compete for the FLN antigen binding site. Since the number of sites is limited, as more sites are occupied by ELN Ab from the sample, fewer sites are left to bind ELN Ab-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The ELN Ab concentration in each sample is interpolated from this standard curve.



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