FIELD: medicine.
SUBSTANCE: method provides using a solid phase of an influenza virus vaccine for sensitisation, whereas antigen-antibody complexes formed by incubating the sensitised surface of an immunosorbent with a test serum containing the influenza virus antibodies are visualised by means of an optical contrast carbon-protein G conjugate for 10-15 minutes.
EFFECT: producing simple, high-sensitive, operative, clear and reliable diagnostic system for estimating a level of post-vaccine immunity to the influenza virus.
1 ex, 1 dwg
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