资料摘要
资料下载The kit assay Human FGF-23 level in the sample，use Purified Human FGF-23 antibody to coat microtiter plate wells, make solid-phase antibody, then add FGF-23 to wells, Combined FGF-23 antibody which With HRP labeled, become antibody - antigen - enzyme-antibody complex, after washing Completely, Add TMB substrate solution,TMB substrate becomes blue color At HRP enzyme-catalyzed, reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. The concentration of Human FGF-23 in the samples is then determined by comparing the O.D. of the samples to the standard curve.
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