Human MPIF 1 ELISA Kit

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  • Alternative name

    C-C motif chemokine 23 ELISA KIT; CK-beta-8 ELISA KIT; CKB-8 ELISA KIT; Macrophage inflammatory protein 3 ELISA KIT; MIP-3 ELISA KIT; Myeloid progenitor inhibitory factor 1 ELISA KIT; MPIF-1 ELISA KIT; Small-inducible cytokine A23Cleaved into the following 4 chains:CCL23(19-99) ELISA KIT; CCL23(22-99) ELISA KIT; CCL23(27-99) ELISA KIT; CCL23(30-99)CCL23 ELISA KIT; MIP3 ELISA KIT; MPIF1 ELISA KIT; SCYA23 ELISA KIT; CKB-8 ELISA KIT; MIP-3 ELISA KIT; MPIF-1 ELISA KIT

  • Catalog
    E025309
  • species
    Human
  • GeneMPIF 1
  • Standard CurveHuman MPIF 1 ELISA Kit
  • Other Species Human MPIF-1/CCL23 ELISA KitHuman MPIF-1 ELISA KitMouse MPIF-1 ELISA Kit
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity1.0 pg/mL.
  • Intended UseHuman MPIF 1 ELISA Kit allows for the in vitro quantitative determination of MPIF 1 , 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
    Principle of the Assay: MPIF-1 ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for MPIF-1. Standards or samples are then added to the microtiter plate wells and MPIF-1 if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of MPIF-1 present in the sample, a standardized preparation of horseradish peroxidase (HRP) -conjugated polyclonal antibody, specific for MPIF-1 are added to each well to "sandwich" the MPIF-1 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 MPIF-1 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 MPIF-1 concentration in each sample is interpolated from this standard curve.



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