摘要:
Die Erfindung betrifft die Verwendung bestimmter Peptide mit extrem hoher Affinität zu anderen Peptiden (Heterodimerbildung) und niedriger Affinität zu sich selbst (Homodimerbildung) im Bereich der in vitro Diagnostik.
摘要:
Immunoassays of improved sensitivity, even when monoclonal antibodies are of poor affinity, are disclosed. An immunoassay method of the invention comprises the steps of: (1) reacting a material to be measured, an immobilized monoclonal antibody (1st antibody) recognizing said material, a monoclonal antibody (2nd antibody) recognizing said material and falling within a different class or subclass fro the 1st antibody, and a labelled antibody (3rd antibody) recognizing the class or subclass of the 2nd antibody to obtain an immuno-complex, and (2) detecting or determining the labelling fragment. In another aspect, the invention provides immunoassay method comprising the steps of: (1) reacts a material to be measured, a protein (the 1st binding protein) to bind specifically to said material, an immobilized protein (the 2nd binding protein) comprising the rest of the 1st binding protein, a part of which having been excised away, and a labelled antibody razing all or part of the excised fragment of the 1st bonding protein to obtain an immuno-complex, and (2) detecting or determining the labelling fragment.
摘要:
An enzyme immunoassay for an antigen using a solid phase, which employs (a) a biotinylated antibody in which a biotin derivative is bound to a thiol group of an Fab′ fragment of an antibody, (b) an enzyme-labelled antibody, and (c) a solid phase immobilized with a substance capable of specifically reacting with the above biotin derivative selected from the group consisting of avidin, streptoavidin and a derivative thereof which is bound to the solid phase directly or via a linkage between another biotin derivative and a high molecular weight substance bound to the solid phase, or alternatively employs (a′) a solid phase immobilized with a biotinylated antibody via a substance selected from the group consisting of avidin, streptoavidin and a derivative thereof wherein said substance is bound to the biotin moiety of said biotinylated antibody and is also bound to the solid phase directly or via a linkage between another biotin derivative and a high molecular weight substance bound to the solid phase, and (b′) an enzyme-labelled antibody, and a solid phase used therefor.
摘要:
Immunoassays of improved sensitivity, even when monoclonal antibodies are of poor affinity, are disclosed. An immunoassay method of the invention comprises the steps of: (1) reacting a material to be measured, an immobilized monoclonal antibody (1st antibody) recognizing said material, a monoclonal antibody (2nd antibody) recognizing said material and falling within a different class or subclass fro the 1st antibody, and a labelled antibody (3rd antibody) recognizing the class or subclass of the 2nd antibody to obtain an immuno-complex, and (2) detecting or determining the labelling fragment. In another aspect, the invention provides immunoassay method comprising the steps of: (1) reacts a material to be measured, a protein (the 1st binding protein) to bind specifically to said material, an immobilized protein (the 2nd binding protein) comprising the rest of the 1st binding protein, a part of which having been excised away, and a labelled antibody razing all or part of the excised fragment of the 1st bonding protein to obtain an immuno-complex, and (2) detecting or determining the labelling fragment.
摘要:
Disclosed is a method for diagnosing cancer by qualitative and quantitative determination according to an immuno-serological assay of cancer-related glycoantigens produced in a body fluid by cancerisation or dedifferentiation of normal cells by determination of the bindability of the glycoantigen to lectin.
摘要:
An improved methodforthe quantitative analysis of antigen by an enzyme-antibody bridge method, which comprises binding (1) an insoluble carrier or a coated insoluble carrier with (2) an antibody being capable of recognizing an antigen (first antibody), (3) an antigen to be determined, (4) arr antibody being capable of recognizing an antigen originated from an animal species different from the animal species of the first antibody (second antibody), (5) an anti-immunoglobulin antibody being capable of recognizing an immunoglobulin of the same animal species as that of the second antibody, (6) an anti-enzyme antibody prepared by using the same animal species as that of the second antibody, (7) an enzyme in this order, and then measuring the amount of the enzyme in the resulting enzyme-anti-enzyme antibody complex, and determining the amount of the antigen therefrom. Said improved method gives a high sensitivity and hence can also be used for the measurement of very low concentration of an antigen.