FIELD: medicine, hematology. SUBSTANCE: method is carried out by the following manner: analyzing extract is added to well cut in agar where the monospecific diagnostic serum is dispersed preliminary. Reaction is carried out in 1.5% agar in barbital-sodium barbital buffer using diagnostic serum with the known content of IgG. The level of IgG is determined in g/l by calibrating curve after measurement of precipitation rings and detected level of immunoglobulins in analyzing object is compared with its minimal level necessary for providing the detection of antigen Glm(1), i. e. 1.4 g/l and above. Based on obtained data the conclusion is made about the blood group by system Gm. Method provides the identification of analyzing blood in particular person. EFFECT: improved assay method.
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Authors
Dates
2004-05-27—Published
2002-03-11—Filed