Human GREM1 ELISA Kit

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  • Alternative name

    Gremlin-1 ELISA KIT; Cell proliferation-inducing gene 2 protein ELISA KIT; Cysteine knot superfamily 1, BMP antagonist 1 ELISA KIT; DAN domain family member 2 ELISA KIT; Down-regulated in Mos-transformed cells protein ELISA KIT; Increased in high glucose protein 2 ELISA KIT; IHG-2GREM1 ELISA KIT; CKTSF1B1 ELISA KIT; DAND2 ELISA KIT; DRM ELISA KIT; PIG2 ELISA KIT; IHG-2 ELISA KIT

  • Catalog
    E017471
  • species
    Human
  • GeneGREM1
  • Standard CurveHuman GREM1 ELISA Kit
  • Other Species Mouse GREM1 ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of GREM1. No significant cross-reactivity or interference between GREM1 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between GREM1 and all the analogues, therefore, cross reaction may still exist in some cases.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity0.1 ng/mL.
  • Intended UseHuman GREM1 ELISA Kit allows for the in vitro quantitative determination of GREM1 , 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: GREM1 ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for GREM1. Standards or samples are then added to the microtiter plate wells and GREM1 if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of GREM1 present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for GREM1 are added to each well to "sandwich" the GREM1 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 GREM1 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 GREM1 concentration in each sample is interpolated from this standard curve.


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