Human LTE4 ELISA Kit

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  • Alternative name

    Lytic transglycosylase, catalytic ELISA KIT; Lytic transglycosylase, catalyticCLP_3833 ELISA KIT;

  • Catalog
  • species
  • GeneLTE4
  • Other Species Mouse LTE4 ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Human LTE4. No significant cross-reactivity or interference between Human LTE4 and analogues was observed. Note: Limited by current skills and knowledge, it is impossible for us to complete the cross- reactivity detection between Human LTE4 and all the analogues, therefore, cross reaction may still exist.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity18.75pg/mL
  • Intended UseHuman LTE4 ELISA Kit allows for the in vitro quantitative determination of LTE4 , 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 LTE4 in human 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 Human LTE4. During the reaction, Human LTE4 in the sample or standard competes with a fixed amount of Human LTE4 on the solid phase supporter for sites on the Biotinylated Detection Ab specific to Human LTE4. 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 Human LTE4 in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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