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  • Alternative name

    Monocyte to macrophage differentiation factor ELISA KIT; Progestin and adipoQ receptor family member 11 ELISA KIT; Progestin and adipoQ receptor family member XIMMD ELISA KIT; PAQR11 ELISA KIT

  • Catalog
  • species
  • GeneMMA
  • Standard CurveHuman MMA ELISA Kit
  • Other Species Human MMA ELISA KitMouse MMA ELISA KitBovine MMA ELISA KitCanine MMA ELISA KitChicken MMA ELISA KitGeneral MMA ELISA KitPorcine MMA ELISA KitRabbit MMA ELISA KitRat MMA ELISA KitCamel MMA ELISA KitGoat MMA ELISA KitGuinea Pig MMA ELISA KitHamster MMA ELISA KitHorse MMA ELISA KitMonkey MMA ELISA KitSheep MMA ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of MMA. No significant cross-reactivity or interference between MMA and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityThe minimum detectable dose of human MMA is typically less than 0.061ng/mL. The sensitivity of this assay, or Lower Limit of Detection (LLD) was defined as the lowest protein concentration that could be differentiated from zero. It was determined by addin
  • Intended UseHuman MMA ELISA Kit allows for the in vitro quantitative determination of MMA , 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
    Principle of the assay: The microtiter plate provided in this kit has been pre-coated with an antibody specific to MMA. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to MMA. 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 MMA, 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 MMA in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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