whole blood, serum, plasma
The AFP Rapid Test Device (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of AFP in whole blood, serum or plasma to aid in the diagnosis of Hepatocellular Carcinoma or fetal open neural tube defects.
Store as packaged inthe sealed pouch either at room temperature or refrigerated (2-30°C). The test device is stable through the expiration date printed on the sealed pouch. The test device must remain in the sealed pouch until use. DO NOT FREEZE.
The AFP Alpha-Fetoprotein Rapid Test Device(Whole Blood/Serum/Plasma) has correctly identified a panel ofspecimensand has been compared to a leading commercial AFP EIA test using clinical specimens. The results show that the relative sensitivity of the AFP Alpha-Fetoprotein Rapid Test Device (Whole Blood/Serum/Plasma) is 99.0%.