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One single mix for testing of six relevant risk factors for thrombophilia.
A test for the detection of the 7 most common variants associated with the risk of developing cardiovascular diseases in one reaction mixture.
Kit enabling the simultaneous detection of the 3 most frequent mutations and the corresponding WT variants in the HFE gene.
NGS kit for the identification of 12 SNPs in polygenic FH & the 6 SNPs to predict statin response.
Kits for the detection of the two most common FII G20210A and FVL G1691A variants associated with the risk of thrombosis.
Kits for the detection of two variants of the MTHFR gene associated with the risk of thrombosis using LAMP technology.
Product for the detection of 4G/5G polymorphism in the promoter of the PAI-1 gene associated with the risk of thrombosis using LAMP technology.
Kit for detecting the two most common variants in the HFE gene using LAMP technology.
Detection of SNV, InDel and CNV germline mutations for a wide range of cardiac and metabolic diseases by NGS.