F2/ F5-SNP

Mutations in the F2 (prothrombin G20210A) and F5 (Factor V Leiden, G1691A) genes are among the most common inherited risk factors for thrombophilia — a condition that increases the risk of abnormal blood clot formation. Detection of these single nucleotide polymorphisms (SNPs) is essential for assessing genetic predisposition to venous thromboembolism and guiding anticoagulant therapy decisions.
F2 / F5-SNP PCR kits based on real-time PCR technology provide a sensitive and specific method for detecting point mutations in the F2 and F5 genes in human genomic DNA. These molecular diagnostics tools offer accurate and reproducible results in routine and specialized laboratory workflows. Available in CE IVD-marked format for diagnostic use and as research use only (RUO) version, these PCR assays support applications such as thrombophilia screening from clinical samples, family risk assessment, and personalized medicine strategies.