A real-time PCR diagnostic test for detecting mutations C282Y and H63D associated with haemochromatosis. The kit provides 2x48 determinations and is used for molecular genetic diagnosis of 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
A genetic diagnostic test for detecting the C282Y mutation in the HFE gene associated with hereditary hemochromatosis. The test kit contains 32 tests and is available for use with QiaSymphony SP/AS extraction systems (reference EER032032QS). It is designed to identify this specific mutation that causes iron metabolism disorders potentially resulting in cirrhosis, hepatoma, heart failure, arrhythmia, and diabetes.
CLONIT SRL · Italy
A genetic diagnostic test for detecting the H63D mutation in the HFE gene associated with hereditary hemochromatosis. The test kit contains 32 tests and is available for use with QiaSymphony SP/AS extraction systems (reference EER33032QS). It identifies this HFE gene mutation involved in intracellular iron transport disorders.
CLONIT SRL · Italy
A genetic diagnostic test for detecting the S65C mutation in the HFE gene associated with hereditary hemochromatosis. The test kit contains 32 tests and is available for use with QiaSymphony SP/AS extraction systems (reference EER031032QS). It is used to identify this mutation responsible for iron metabolism disorders.
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