Mouse TFR ELISA Kit

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  • Alternative name

    Transferrin receptor protein 1 ELISA KIT; T9 ELISA KIT; p90 ELISA KIT; CD_antigen: CD71TFRC ELISA KIT; TR ELISA KIT; TfR ELISA KIT; TfR1 ELISA KIT; Trfr ELISA KIT; sTfR ELISA KIT

  • Catalog
    E070670
  • species
    Mouse
  • GeneTFR
  • Standard CurveMouse TFR ELISA Kit
  • Other Species Human TFR/CD71 ELISA KitHuman TFR ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of TFR. No significant cross-reactivity or interference between TFR and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityThe minimum detectable dose of TFR is typically less than 0.122ng/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 adding two
  • Intended UseMouse TFR ELISA Kit allows for the in vitro quantitative determination of TFR , 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 microtiter plate provided in this kit has been pre-coated with an antibody specific to TFR. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to TFR. 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 TFR, 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 TFR in the samples is then determined by comparing the O.D. of the samples to the standard curve.


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