GABA (GABA) Rapid ELISA kit

This Rapid ELISA kit applies Competitive Inhibition enzyme immunoassay technique for the quantitative detection. The micro ELISA plate provided in this kit has been pre-coated with gABA. During the reaction, gABA in the sample or standard competes with a fixed amount of gABA on the solid phase supporter for sites on the Biotinylated Detection Ab specific to gABA. Excess conjugate and unbound sample or standard are washed away, and Avidin-Horseradish Peroxidase (HRP) conjugate are added to each micro plate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns from blue to yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of gABA in tested samples can be calculated by comparing the OD of the samples to the standard curve.