We are proud to be the sole distributors of CE-IVD certified kits available on the market for SNP analysis based on LAMP technology produced by LACAR MDX Technologies (Belgium). The kits do not require DNA extraction. We offer a variety of panels, including pharmacogenetics, coagulation, and food intolerance.
The LAMP Human 2nd MTHFR mutation KIT is an in vitro diagnostic test intended for the qualitative detection of the methylenetetrahydrofolate reductase (MTHFR) A1298C mutation
The LAMP Human A1AT KIT is an in vitro diagnostic test intended for the qualitative detection of two SERPINA1 alleles, Pi*Z and Pi*S
The LAMP Human CYP2C19 deficiency KIT is an in vitro diagnostic test intended for the qualitative detection of three less functional CYP2C19 alleles (*2, *3, *17)
The LAMP Human CYP2C9 deficiency KIT is an in vitro diagnostic test intended for the qualitative detection of two less functional CYP2C9 alleles (*2, *3)
The LAMP Human DPD4var KIT is an IVDR diagnostic test for the qualitative detection of four different non-functional or less functional DPYD alleles.
The LAMP Human DPD5var KIT is an IVDR diagnostic test for the qualitative detection of five different non-functional or less functional DPYD alleles.
The KIT LAMP Human DPD7 is a diagnostic test for the qualitative detection of the non-functional allele DPDY*7.
The LAMP Human Hemochromatosis 3mut KIT is an in vitro diagnostic test intended for the qualitative detection of the mutations C282Y (rs1800562), H63D (rs1799945) and S65C (rs1800730)
The LAMP Human Prothrombin mutation KIT is an in vitro diagnostic test intended for the qualitative detection of Factor II G20210A
The LAMP Human FII&FVL duplex KIT is an in vitro diagnostic test intended for the qualitative detection of the Factor II G20210A and the Factor V Leiden G1691A polymorphisms
The LAMP Human FV LEIDEN mutation KIT is an in vitro diagnostic test intended for the qualitative detection of Factor V Leiden G1691A
The LAMP Human Fructose Intolerance KIT is an in vitro diagnostic test intended for the qualitative detection of the mutation rs1800546
