| Assay principle |
Enzyme Immunoassay for the quantitative determination of dopamine. Flexible test system for various biological sample types and volumes.
Dopamine is extracted by using a cis-diol-specific affinity gel, acylated and then converted enzymatically.
The competitive ELISA kit uses the microtiter plate format. The antigen is bound to the solid phase of the microtiter plate. The derivatized standards, controls and samples and the solid phase bound analyte compete for a fixed number of antibody binding sites. After the system is in equilibrium, free antigen and free antigen-antibody complexes are removed by washing. The antibody bound to the solid phase is detected by an anti-rabbit IgG-peroxidase conjugate using TMB as a substrate. The reaction is monitored at
450 nm.
Quantification of unknown samples is achieved by comparing their absorbance with a standard curve prepared with known standard concentrations.
|
