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
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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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.
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 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.
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.
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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.
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.
AB ANALITICA Srl · Italy
A molecular diagnostic test for HFE gene C282Y mutation detection. This test is used in hemochromatosis screening and genetic assessment.
AB ANALITICA Srl · Italy
A molecular diagnostic test for HFE gene H63D mutation detection. This test is used in hemochromatosis genetic assessment.
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Kit for detecting the S65C mutation of HFE gene by Real Time PCR using TaqMan® probes technology. This diagnostic kit identifies mutations in the HFE gene associated with iron metabolism disorders.
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