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Use: This test is intended to be used as an aid to the diagnosis of human granulocytic anaplasmosis (HGA), a condition formerly known as human granulocytic ehrlichiosis (HGE) caused by Anaplasma phagocytophilum.
Limitations:This test was developed and its performance characteristics determined by Labcorp. It has not been cleared or approved by the Food and Drug Administration.
Methodology: Polymerase chain reaction (PCR)
Collection Instructions:
Specimen: Whole blood
Volume: 1 mL
Minimum Volume: 0.2 mL
Container: Lavender-top (EDTA) tube or yellow-top (ACD) tube
Storage Instructions: Refrigerate.
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