Human SGLT1 ELISA Kit

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  • Alternative name

    Sodium/glucose cotransporter 1 ELISA KIT; High affinity sodium-glucose cotransporter ELISA KIT; Solute carrier family 5 member 1Slc5a1 ELISA KIT; Na(+)/glucose cotransporter 1 ELISA KIT

  • Catalog
    E035615
  • species
    Human
  • GeneSGLT1
  • Standard CurveHuman SGLT1 ELISA Kit
  • Other Species Mouse SGLT1 ELISA Kit
  • SpecificityThis assay has high sensitivity and excellent specificity for detection of SGLT1. No significant cross-reactivity or interference between SGLT1 and analogues was observed.
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • SensitivityThe minimum detectable dose of human SGLT1 is typically less than 0.056ng/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 add
  • Intended UseHuman SGLT1 ELISA Kit allows for the in vitro quantitative determination of SGLT1 , 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 SGLT1. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to SGLT1. 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 SGLT1, 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 SGLT1 in the samples is then determined by comparing the O.D. of the samples to the standard curve.




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