FiCA™ CEA is a fluorescence immunoassay (FIA) for quantitative determination of carcinoembryonic antigen (CEA) in human serum, plasma and whole blood. It is used for the monitoring of patients with tumor after radiation therapy or surgery.
For in vitro diagnostic use only. For professional use only.
TEST PRINCIPLE
This kit uses double antibody sandwich method and fluorescence immunochromatography technology to quantitatively detect the concentration of AFP in human serum, plasma, and whole blood samples.
DETECTION RANGE: 1-500 ng/mL
APPLICABLE INSTRUMENT
FiCA™ tests only can be performed with FiCA™ analyzers.
STORAGE
Test Kits should be stored at 2°C~30°C in a cool, dark, dry place, valid for 24 months; Do not freeze or use after the period of validity by all means.