Human LN11 ELISA Kit

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  • Alternative name

    Laminin subunit gamma-1 ELISA KIT; Laminin B2 chain ELISA KIT; Laminin-1 subunit gamma ELISA KIT; Laminin-10 subunit gamma ELISA KIT; Laminin-11 subunit gamma ELISA KIT; Laminin-2 subunit gamma ELISA KIT; Laminin-3 subunit gamma ELISA KIT; Laminin-4 subunit gamma ELISA KIT; Laminin-6 subunit gamma ELISA KIT; Laminin-7 subunit gamma ELISA KIT; Laminin-8 subunit gamma ELISA KIT; Laminin-9 subunit gamma ELISA KIT; S-laminin subunit gamma ELISA KIT; S-LAM gammaLAMC1 ELISA KIT; LAMB2 ELISA KIT; S-LAM gamma ELISA KIT

  • Catalog
    E022148
  • species
    Human
  • GeneLN11
  • Standard CurveHuman LN11 ELISA Kit
  • Other Species Mouse LN11 ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of LN11. No significant cross-reactivity or interference between LN11 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between LN11 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 LN11 ELISA Kit allows for the in vitro quantitative determination of LN11 , 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
    specifical
    Principle of the assay: LN11 ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-LN11 antibody and an LN11-HRP conjugate. The assay sample and buffer are incubated together with LN11-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 LN11 concentration since LN11 from samples and LN11-HRP conjugate compete for the anti-LN11 antibody binding site. Since the number of sites is limited, as more sites are occupied by LN11 from the sample, fewer sites are left to bind LN11-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The LN11 concentration in each sample is interpolated from this standard curve.



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