FIELD: medicine. SUBSTANCE: method involves covering solid body carrier having twelve various conditionally pathogenic bacteria antigens absorbed thereon with control serum and sera under study in working dilution of 1:100 - 1: 1600. Immunoenzyme analysis is carried out and optical density of the control serum and sera under study is measured to determine difference between optical density of sample under study and negative control sample. The value being equal to or greater than 0.3, increased humoral immunity to conditionally pathogenic bacteria is considered to be the case. EFFECT: high accuracy of the method. 6 tbl
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Authors
Dates
2003-10-10—Published
2002-09-19—Filed