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
Specimen requirements
Serum (50 ul) is the recommended sample type for this assay
Turnaround time
24 hours