Mouse LNGFR ELISA Kit

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  • Alternative name

    Tumor necrosis factor receptor superfamily member 16 ELISA KIT; Gp80-LNGFR ELISA KIT; Low affinity neurotrophin receptor p75NTR ELISA KIT; Low-affinity nerve growth factor receptor ELISA KIT; NGF receptor ELISA KIT; p75 ICD ELISA KIT; CD_antigen: CD271Ngfr ELISA KIT; Tnfrsf16 ELISA KIT; NGF receptor ELISA KIT

  • Catalog
    E058933
  • species
    Mouse
  • GeneLNGFR
  • Standard CurveMouse LNGFR ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of LNGFR. No significant cross-reactivity or interference between LNGFR and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity0.058ng/mL.
  • Intended UseMouse LNGFR ELISA Kit allows for the in vitro quantitative determination of LNGFR , 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
    Intended Uses: The kit is a sandwich enzyme immunoassay for in vitro quantitative measurement of LNGFR in mouse serum, plasma, tissue homogenates and other biological fluids. Principle of the Assay||The microtiter plate provided in this kit has been pre-coated with an antibody specific to LNGFR. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to LNGFR. 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 LNGFR, 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 LNGFR in the samples is then determined by comparing the O.D. of the samples to the standard curve.



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