Fast and Easy Detection of FII
Lamp Human Prothrombin mutation kit (rs1799963)
Risk Factors of Genetic Thrombosis:
An in vitro diagnostic test that allows the detection and genotyping of a single point mutation (G20210A) of the human Factor II gene, referred to as Factor II mutation, directly from human whole blood.
Clotting factor II, or prothrombin, is a vitamin K–dependent proenzyme that functions in the blood coagulation cascade. Factor II deficiency is a common, inherited or acquired bleeding disorder.
Inherited factor II deficiency is an autosomal recessive disorder that can manifest as hypoprthrombinemia ,a decrease in the overall synthesis of prothrombin, or as dysprothrombinemia, the synthesis of dysfunctional prothrombin.*1
• RAPIDITY: 1 minute hand-time & 30 minutes amplification + detection
• SIMPLICITY: No laborious DNA extraction procedure
• EFFICIENCY: Perfect distinction of the heterozygote