The basis of ELISA is the immobilization of antigen or antibody and the enzymatic labeling of antigen or antibody. The antigen or antibody bound to the surface of the solid support still retains its immunological activity, and the enzyme-labeled antigen or antibody retains its immunological activity, and Retaining the activity of the enzyme. At the time of measurement, the test specimen (the antibody or antigen therein is reacted) reacts with the antigen or antibody on the surface of the solid phase carrier. The antigen-antibody complex formed on the solid phase carrier is mixed with the liquid by washing. The other substances are separated. The enzyme-labeled antigen or antibody is further added to the solid phase carrier by the reaction. At this time, the amount of the enzyme on the solid phase is proportional to the amount of the test substance in the sample. After the substrate, the substrate is catalyzed by the enzyme to become a colored product. The amount of the product is directly related to the amount of the substance to be tested in the sample, so that it can be qualitatively or quantitatively analyzed according to the depth of the color. Due to the high catalytic efficiency of the enzyme, indirectly Amplified the results of the immune response, making the measurement method achieve high sensitivity. Shanghai Jinma Bioanalysis
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