FIELD: medicine.
SUBSTANCE: it involves sampling of immune specific serums containing antibodies to basic virus antigens and having various concentrations of these antibodies, and also sampling of healthy donor serums with a null titre. Serum sampling for a performance panel is ensured by the PCR-analysis data for viral RNA and separate protein titration in immune-enzyme assay. The immune specific serums are those which have the optical density shown by immune-enzyme assay less than a critical optical density.
EFFECT: method enables a correct assessment of serologic assay data and higher quality control of sensitivity and specificity of test systems and immunoblots.
6 cl, 1 ex
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Authors
Dates
2010-12-27—Published
2009-03-26—Filed