Human CHRM2 Ab ELISA Kit

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  • Alternative name

    Muscarinic acetylcholine receptor M2 ELISA KIT; CHRM2 ELISA KIT;

  • Catalog
    E008267
  • species
    Human
  • GeneCHRM2 Ab
  • Standard CurveHuman CHRM2 Ab ELISA Kit
  • Other Species Mouse CHRM2 Ab ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of CHRM2-Ab. No significant cross-reactivity or interference between CHRM2-Ab and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between CHRM2-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 CHRM2 Ab ELISA Kit allows for the in vitro quantitative determination of CHRM2 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/FamilyImmunology
  • Product Description
    specifical
    Intended Uses: This CHRM2-Ab ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human CHRM2-Ab. This ELISA kit for research use only, not for therapeutic or diagnostic applications! Principle of the Assay||CHRM2-Ab ELISA kit applies the competitive enzyme immunoassay technique utilizing a CHRM2 antigen and an CHRM2-Ab-HRP conjugate. The assay sample and buffer are incubated together with CHRM2-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 CHRM2-Ab concentration since CHRM2-Ab from samples and CHRM2-Ab-HRP conjugate compete for the CHRM2 antigen binding site. Since the number of sites is limited, as more sites are occupied by CHRM2-Ab from the sample, fewer sites are left to bind CHRM2-Ab-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The CHRM2-Ab concentration in each sample is interpolated from this standard curve.




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