Genetic Thrombosis
Thrombophilia is a predisposition to abnormal blood clotting. Its inherited forms arise from variants in genes involved in coagulation and fibrinolysis. Identifying these variants supports individual risk assessment, particularly in patients with a personal or family history of thrombosis, recurrent pregnancy loss, or before hormonal treatment or surgery.
The kits below cover each marker individually or in duplex, run from the primary sample under CE-IVD.
The LAMP Human Prothrombin mutation KIT is an in vitro diagnostic test intended for the qualitative detection of Factor II G20210A by Loop-mediated isothermal amplification (LAMP) on EDTA whole blood and extracted DNA.
The LAMP Human FV LEIDEN mutation KIT is an in vitro diagnostic test intended for the qualitative detection of Factor V Leiden G1691A by Loop-mediated isothermal amplification (LAMP) on EDTA whole blood and extracted DNA.
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 by Loop-mediated isothermal amplification (LAMP) on EDTA whole blood and extracted DNA.
The LAMP Human MTHFR mutation KIT is an in vitro diagnostic test intended for the qualitative detection of the methylenetetrahydrofolate reductase (MTHFR) C677T mutation by Loop-mediated isothermal amplification (LAMP) on EDTA whole blood and extracted DNA.
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 by Loop-mediated isothermal amplification (LAMP) on EDTA whole blood and extracted DNA.
The LAMP Human PAI-1 mutation KIT is an in vitro diagnostic test intended for the qualitative detection of PAI-1 insertion/deletion (5G/4G) by Loop-mediated isothermal amplification (LAMP) on EDTA whole blood and extracted DNA.
Autoimmune Diseases
HLA-B27 is associated with the spondyloarthropathies, including ankylosing spondylitis and acute anterior uveitis. Typing contributes to the diagnostic work-up of patients with suggestive symptoms.
LaCAR offers CE-IVD HLA-B27 assays.
LaCAR offers CE-IVD HLA-B27 assays.
Food Intolerance
Genotyping identifies the genetic basis of primary lactose intolerance (lactase non-persistence) and the HLA-DQ2/DQ8 haplotypes associated with coeliac disease.
LaCAR provides CE-IVD kits for these markers, run from the primary sample.
LaCAR provides CE-IVD kits for these markers, run from the primary sample.
Others
Additional inherited conditions where genotyping informs clinical management, including hereditary hemochromatosis (HFE) and alpha-1 antitrypsin deficiency (SERPINA1).
LaCAR provides CE-IVD kits for SNP detection in these conditions.
LaCAR provides CE-IVD kits for SNP detection in these conditions.
You have a question regarding our products ? You want to know more about our method ?
Find out about our other expertises
Genetic testing
CE Kits
Newborn Screening
Genetic testing
CE Kits
Pharmacogenetics
