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Human Nesp1 ELISA Kit

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  • Alternative name

    Nesprin-1 ELISA KIT; Enaptin ELISA KIT; Myocyte nuclear envelope protein 1 ELISA KIT; Myne-1 ELISA KIT; Nuclear envelope spectrin repeat protein 1 ELISA KIT; Synaptic nuclear envelope protein 1 ELISA KIT; Syne-1SYNE1 ELISA KIT; C6orf98 ELISA KIT; KIAA0796 ELISA KIT; KIAA1262 ELISA KIT; KIAA1756 ELISA KIT; MYNE1 ELISA KIT; Myne-1 ELISA KIT; Syne-1 ELISA KIT
  • Catalog
    E025993
  • species
    Human
  • GeneNesp1
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of Nesprin 1 (Nesp1). No significant cross-reactivity or interference between Nesprin 1 (Nesp1) and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityTypically less than 0.105ng/mL.
  • Intended UseHuman Nesp1 ELISA Kit allows for the in vitro quantitative determination of Nesp1 , 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 Nesprin 1 (Nesp1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Nesprin 1 (Nesp1). 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 Nesprin 1 (Nesp1), 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 Nesprin 1 (Nesp1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.



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