Human PGDS ELISA Kit

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  • Alternative name

    Hematopoietic prostaglandin D synthase ELISA KIT; GST class-sigma ELISA KIT; Glutathione S-transferase (EC:2.5.1.18) ELISA KIT; Glutathione-dependent PGD synthase ELISA KIT; Glutathione-requiring prostaglandin D synthase ELISA KIT; Prostaglandin-H2 D-isomeraseHPGDS ELISA KIT; GSTS ELISA KIT; PGDS ELISA KIT; PTGDS2 ELISA KIT; H-PGDS ELISA KIT

  • Catalog
    E031253
  • species
    Human
  • GenePGDS
  • Other Species Human L PGDS ELISA KitHuman L-PGDS ELISA KitMouse L-PGDS ELISA KitMouse PGDS ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of human PGDS. No significant cross-reactivity or interference between human PGDS and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityThe minimum detectable dose of human PGDS is typically less than 0.078 ng/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 the me
  • Intended UseHuman PGDS ELISA Kit allows for the in vitro quantitative determination of PGDS , 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: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for PGDS has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any PGDS present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for PGDS is added to the wells. After washing, avidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PGDS bound in the initial step. The color development is stopped and the intensity of the color is measured.



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