Enzyme Immunoassay for the quantitative determination of 5-Hydroxy-3-Indole Acetic Acid (5-HIAA) in urine. First, 5-HIAA is derivatized by methylation. The subsequent competitive ELISA uses the microtiter plate format. The antigen is bound to the solid phase of the microtiter plate. The methylated analyte in the standards, controls and samples and the solid phase bound analyte compete for a fixed number of antibody binding sites. After the system has reached 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. NAME: 5-HIAA ELISADESCRIPTION: Enzyme immunoassay (ELISA) for the quantitative determination of 5-HIAA (5-hydroxyindoleacetic acid)DESIGN: Common sample preparation. 6 Standards. 2 Controls. ready for use.SAMPLE VOLUME: 50 µl urineTOTAL ASSAY TIME: Sample preparation 20 min and ELISA 2.5 hSTANDARD RANGE: 0 / 0.5 - 50 mg/lSENSITIVITY: 0.17 mg/lSTORAGE: 2 - 8 ° CKIT: 96 DeterminationsADVANTAGES: No interference by medical drugs knownWide standard ranges. convenient measurement of pathological samples without predilutionCE MARK: CE Marked
Academic Discount – Customers performing Academic Research are entitled to a 10% discount on all Coagulation and Biochemistry products. Use Voucher Code ACAD10 at checkout.