A diagnostic test kit for detecting mutations C282Y and H63D in the HFE gene associated with hereditary hemochromatosis. The kit contains 2x20 test determinations and is used to identify genetic variants related to iron metabolism disorders.
Manufactured by
Attomol GmbH - Molekulare Diagnostika
Bronkow, Germany
Driving Diagnostic Excellence: Attomol - Where Expertise Meets Innovation. With over two decades of unwavering commitment, our owner-managed company, deeply rooted in Lusatia (Brandenburg), comprises a team of 30+ highly qualified professionals. We embody values of honesty, openness, and mutual respect, serving the global laboratory medicine community with patented, reliable diagnostic tools. Specializing in mutation detection, autoantibody tests, and multiplex bead assays , our advanced solutions streamline daily workflows. At Attomol, our dedicated team defines our identity, delivering sophisticated test systems and unparalleled expert support. Customer satisfaction is our top priority, with prompt responses and steadfast assistance. We express gratitude for our robust network, cultivated through memberships in DiagnostikNet-BB e.V. and BioResponse e.V. Join us in advancing diagnostic capabilities – Attomol, Precision in Every Test .
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CLONIT SRL
Italy · 21 relevant products
Operon S.A.
Spain · 2 relevant products
GENERI BIOTECH s.r.o.
Czech Republic · 6 relevant products
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CLONIT SRL · Italy
A comprehensive genetic diagnostic test kit for detecting three HFE gene mutations (C282Y, H63D, and S65C) associated with hereditary hemochromatosis. The kit contains 40 tests and uses real-time quantitative PCR (RQ) methodology to identify mutations that cause iron metabolism disorders and associated complications including cirrhosis, hepatoma, heart failure, and diabetes.
Operon S.A. · Spain
A molecular diagnostic test for the detection of hemochromatosis genetic mutations in human samples. Used for in vitro diagnosis of hereditary hemochromatosis.
GENERI BIOTECH s.r.o. · Czech Republic
CE IVD real-time PCR kit for detection of HFE gene mutations associated with hereditary hemochromatosis in human genomic DNA. Facilitates early identification and management of iron overload disorders.
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