Human IL-7 ELISA Kit is based on the quantitative sandwich enzyme-linked immunosorbent assay technique to measure concentration of human IL-7 in the samples. A monoclonal antibody specific for human IL-7 has been immobilized onto microwells. Standard or samples are pipetted into the wells, followed by the addition of biotin-linked monoclonal antibody specific for IL-7, and IL-7 present is bound by the immobilized antibody and detect antibody following the first incubation. After removal of any unbound substances, streptavidin-HRP is added for a second incubation. After washing, substrate solution reacts with HRP and color develops in proportion to the amount of IL-7 bound by the immobilized antibody. The color development is stopped by addition of acid and the optical density value is measured by microplate reader.
Plate-forme
Microplate
Méthode de détection
Colorimetric
Type d'échantillon
Cell culture supernatant, serum and plasma.
Sensibilité
0.22 pg/ml
Gamme de detection
7.81 - 500 pg/ml
Récupération
101% (Average Recovery from Serum Samples).
Spécificité
This kit can assay both natural and recombinant human IL-7.
Reactivité
Human
Réactivité croisée
This assay has shown no significant cross-reactivity.