Hemochromatosis
Hereditary hemochromatosis (HH) is a recessive genetic disorder characterized by an increased intestinal iron absorption resulting in systemic iron overload, especially in the liver, pancreas, joints and testes. If untreated, HH can cause liver fibrosis, cirrhosis and hepatocellular carcinoma. HH is commonly caused by certain variants in the HFE gene.
The LAMP Human Hemochromatosis KIT is an in vitro diagnostic test intended for the qualitative detection of the mutations C282Y (rs1800562) and H63D (rs1799945) on EDTA whole blood and extracted DNA.
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) on EDTA whole blood and extracted DNA.
Genetic Thrombosis
Explore our specialized kits and consumables designed for reliable and fast detection.
Easily identify common SNPs directly from the primary sample with our CE-IVD certified solution.
Easily identify common SNPs directly from the primary sample with our CE-IVD certified solution.
Autoimmune Diseases
Our innovative kits and consumables simplify the detection of autoimmune markers.
Achieve precise results directly from the initial sample with our proven CE-IVD technology.
Achieve precise results directly from the initial sample with our proven CE-IVD technology.
Food Intolerance
Streamline the detection of food intolerances with our advanced kits.
A quick and efficient solution to analyze the primary sample, backed by CE-IVD certification.
A quick and efficient solution to analyze the primary sample, backed by CE-IVD certification.
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