This Fibronectin enzyme linked immunosorbent assay (ELISA) applies a technique called a quantitative sandwich immunoassay. The microtiter plate has been pre-coated with an Anti-Fibronectin Antibody. Standards or samples are then added to the microtire plate wells and Fibronectin, if present, will bind to the antibody pre-coated on the wells. In order to quantify the amount of Fibronectin present in the sample, Anti-Fibronectin Antibody (Biotin) is added to each well to "sandwich" the Fibronectin immobilised on the plate. The microtiter plate then undergoes incubation, followed by thorough washing of the wells to remove all unbound components. Next, Avidin-Biotin-Peroxidase Complex is added to each well for a short incubation period, followed by thorough washing of the wells to remove all unbound conjugates. Next, a TMB (3,3',5,5' tetramethyl-benzidine) substrate solution is added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period. Only those wells that contain Fibronectin will exhibit a change in colour. The enzyme-substrate reaction is terminated by the addition of a stop solution and the colour change is measured spectrophotometrically at a wavelength of 450nm ± 2nm.
Plate-forme
Microplate
Méthode de détection
Colorimetric
Type d'échantillon
Serum, plasma, body fluids, tissue lysates, and cell culture supernatants.
Sensibilité
< 10 pg/ml
Gamme de detection
156-10,000 pg/ml
Reactivité
Human
Precision
Intra-assay CV: < 8%, Inter-assay CV: < 10%
Stockage
Store at 2-8°C for 4 months or at -20°C for 8 months.
