Clinical Use:
Background: For in vitro diagnostic use in the quantitative determination of carcinoembryonic antigen (CEA) in serum to aid in the management of cancer patients in whom changing concentrations of CEA are observed using the ADVIA Centaur and ADVIA Centaur XP systems.
Reference Ranges: 0 – 2.5 µg/L
Associated Diseases:
Patient Preparation:
Specimen Requirements: Serum (50 ul) is the recommended sample type for this assay
Turnaround Time: 24 hours
Additional Information:
Referred Test: