Human CGRP ELISA Kit

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  • Alternative name

    Calcitonin gene-related peptide ELISA KIT; CALCA ELISA KIT; CALC ELISA KIT; CGRP ELISA KIT

  • Catalog
    E005961
  • species
    Human
  • GeneCGRP
  • Standard CurveHuman CGRP ELISA Kit
  • Other Species Mouse CGRP ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of CGRP. No significant cross-reactivity or interference between CGRP and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between CGRP and all the analogues, therefore, cross reaction may still exist in some cases.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity1.0pg/mL.
  • Intended UseHuman CGRP ELISA Kit allows for the in vitro quantitative determination of CGRP , 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/FamilyNeurobiology
  • Product Description
    specifical
    Intended Uses||This CGRP ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human CGRP. This ELISA kit for research use only, not for therapeutic or diagnostic applications! Principle of the Assay: CGRP ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for CGRP. Standards or samples are then added to the microtiter plate wells and CGRP if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of CGRP present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for CGRP are added to each well to "sandwich? the CGRP immobilized on the plate. The microtiter plate undergoes incubation, and then the wells are thoroughly washed to remove all unbound components. Next, substrate solutions are added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period. Only those wells that contain CGRP and enzyme-conjugated antibody will exhibit a change in color. The enzyme-substrate reaction is terminated by addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The CGRP concentration in each sample is interpolated from this standard curve.




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