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  • Alternative name

    Excitatory amino acid transporter 2 ELISA KIT; Glutamate/aspartate transporter II ELISA KIT; Sodium-dependent glutamate/aspartate transporter 2 ELISA KIT; Solute carrier family 1 member 2SLC1A2 ELISA KIT; EAAT2 ELISA KIT; GLT1 ELISA KIT

  • Catalog
  • species
  • GeneEAAT2
  • Standard CurveHuman EAAT2 ELISA Kit
  • Other Species Mouse EAAT2 ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of EAAT2. No significant cross-reactivity or interference between EAAT2 and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityThe minimum detectable dose of EAAT2 is typically less than 0.117ng/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 tw
  • Intended UseHuman EAAT2 ELISA Kit allows for the in vitro quantitative determination of EAAT2 , 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
    Principle of the assay: The microtiter plate provided in this kit has been pre-coated with an antibody specific to EAAT2. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to EAAT2. 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 EAAT2, 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 EAAT2 in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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