FIELD: medicine, veterinary science, food and pharmaceutical industry. SUBSTANCE: for assay carrying out DNA is isolated from blood sample and polymerase chain reaction (PCR) is carried out. Primers for nucleotide sequence that is general for all microorganisms are used in PCR and reaction is carried out in the presence of internal standard of competitive type. Signals from internal standard and for nucleotide sequence that is general for all microorganisms are detected. Bacterial blood contamination is determined in the case of simultaneous presence of signals from internal standard and from nucleotide sequence that is general for all microorganisms. The absence of bacterial contamination is determined in the case of signal from a single internal standard only. Invention can be used for direct gene testing bacterial contamination of donor blood and its components. EFFECT: enhanced precision of detection of contaminants. 5 dwg, 2 tbl, 4 ex
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Authors
Dates
2003-07-20—Published
2002-08-28—Filed