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Human F13 ELISA Kit

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  • Alternative name

    Coagulation factor XIII A chain ELISA KIT; Protein-glutamine gamma-glutamyltransferase A chain ELISA KIT; Transglutaminase A chainF13A1 ELISA KIT; F13A ELISA KIT; Coagulation factor XIIIa ELISA KIT
  • Catalog
    E009866
  • species
    Human
  • GeneF13
  • Standard CurveHuman F13 ELISA Kit
  • Other Species Mouse F13 ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Coagulation Factor XIII (F13). No significant cross-reactivity or interference between Coagulation Factor XIII (F13) and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityTypically less than 9.5pg/mL.
  • Intended UseHuman F13 ELISA Kit allows for the in vitro quantitative determination of F13 , 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 Coagulation Factor XIII (F13). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Coagulation Factor XIII (F13). 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 Coagulation Factor XIII (F13), 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 Coagulation Factor XIII (F13) in the samples is then determined by comparing the O.D. of the samples to the standard curve.


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