SpecificityThis assay has high sensitivity and excellent specificity for detection of Human deltaSIP-alpha. No significant cross-reactivity or interference between Human deltaSIP-alpha and analogues was observed. Note: Limited by current skills and knowledge, it is impossible for us to complete the cross- reactivity detection between Human deltaSIP-alpha and all the analogues, therefore, cross reaction may still exist.
Intended UseHuman deltaSIP-alpha ELISA Kit allows for the in vitro quantitative determination of deltaSIP-alpha , 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 specificalDescription: The kit is a competitive enzyme immunoassay for in vitro quantitative measurement of deltaSIP-alpha in human serum, plasma and other biological fluids
Principle of the Assay: This ELISA kit uses Competitive-ELISA as the method. The microtiter plate provided in this kit has been pre-coated with Human deltaSIP-alpha. During the reaction, Human deltaSIP-alpha in the sample or standard competes with a fixed amount of Human deltaSIP-alpha on the solid phase supporter for sites on the Biotinylated Detection Ab specific to Human deltaSIP-alpha. Excess conjugate and unbound sample or standard are washed from the plate, and Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm +/- 2 nm. The concentration of Human deltaSIP-alpha in the samples is then determined by comparing the O.D. of the samples to the standard curve.