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Detection of IgM antibodies to Brucella abortus in human sera
This test was developed, and its performance characteristics determined, by LabCorp. It has not been cleared or approved by the US Food and Drug Administration (FDA).
Enzyme immunoassay (EIA)
Specimen should be free of bacterial contamination, hemolysis, and lipemia.
Maintain specimen at room temperature.
Causes for Rejection
Hemolysis; lipemia; gross bacterial contamination
|Order Code||Order Code Name||Order Loinc||Result Code||Result Code Name||UofM||Result LOINC|
|164624||Brucella Antibody IgM, EIA||24388-1||164050||Brucella Antibody IgM, EIA||24388-1|