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Human MPIF1 ELISA Kit

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  • Alternative name

    C-C motif chemokine 23 ELISA KIT; CK-beta-8 ELISA KIT; CKB-8CCL23 ELISA KIT; MIP3 ELISA KIT; MPIF1 ELISA KIT; SCYA23 ELISA KIT; CKB-8 ELISA KIT; MIP-3 ELISA KIT; MPIF-1 ELISA KIT
  • Catalog
    E025312
  • species
    Human
  • GeneMPIF1
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Myeloid Progenitor Inhibitory Factor 1 (MPIF1). No significant cross-reactivity or interference between Myeloid Progenitor Inhibitory Factor 1 (MPIF1) and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityTypically less than 0.47pg/mL.
  • Intended UseHuman MPIF1 ELISA Kit allows for the in vitro quantitative determination of MPIF1 , 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: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Myeloid Progenitor Inhibitory Factor 1 (MPIF1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Myeloid Progenitor Inhibitory Factor 1 (MPIF1). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Myeloid Progenitor Inhibitory Factor 1 (MPIF1), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Myeloid Progenitor Inhibitory Factor 1 (MPIF1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.



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