Mouse PGF2alpha ELISA Kit

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  • Alternative name

    Prostaglandin F2-alpha receptor ELISA KIT; Prostanoid FP receptorPTGFR ELISA KIT; PGF receptor ELISA KIT; PGF2-alpha receptor ELISA KIT

  • Catalog
  • species
  • GenePGF2alpha
  • Other Species Human PGF2alpha ELISA KitHuman 8-epi-PGF2alpha ELISA KitHuman 9alpha, 11beta PGF2alpha ELISA KitMouse 8-epi-PGF2alpha ELISA KitMouse 9alpha, 11beta PGF2alpha ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Mouse PGF2alpha. No significant cross-reactivity or interference between Mouse PGF2alpha and analogues was observed. Note: Limited by current skills and knowledge, it is impossible for us to complete the cross- reactivity detection between Mouse PGF2alpha and all the analogues, therefore, cross reaction may still exist.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity9.375pg/mL
  • Intended UseMouse PGF2alpha ELISA Kit allows for the in vitro quantitative determination of PGF2alpha , 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
    Description: The kit is a competitive enzyme immunoassay for in vitro quantitative measurement of PGF2alpha in Mouse serum, plasma and other biological fluids Principle of the Assay: This ELISA kit uses Competitive-ELISA as the method. The microtiter plate provided in this kit has been pre-coated with Mouse PGF2alpha. During the reaction, Mouse PGF2alpha in the sample or standard competes with a fixed amount of Mouse PGF2alpha on the solid phase supporter for sites on the Biotinylated Detection Ab specific to Mouse PGF2alpha. Excess conjugate and unbound sample or standard are washed from the plate, and Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm +/- 2 nm. The concentration of Mouse PGF2alpha in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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