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
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 .
✦ Product-Specific Coverage
Based on AI-matched alternatives related to this product across Suplivia's medical sourcing network.
Generated for this product
AI-matched supplier coverage based on related product alternatives.
CLONIT SRL
Italy · 21 relevant products
Operon S.A.
Spain · 2 relevant products
GENERI BIOTECH s.r.o.
Czech Republic · 6 relevant products
AB ANALITICA Srl
Italy · 2 relevant products
Blackhills Diagnostic Resources, S.L.U. BDR
Spain · 2 relevant products
Fosun Diagnostics (Shanghai) Co., Ltd
China · 1 relevant product
He Bei GuoGao BiotechnoLogy co .,ltd
China · 1 relevant product
AEHEALTH Limited
China · 1 relevant product
Zeesan Biotech Co., Ltd
China · 1 relevant product
Zhuhai Encode Medical Engineering Co Ltd
China · 1 relevant product
32 more relevant manufacturers available
Get free access to all relevant manufacturers for this product.
See all manufacturers →7 more sourcing countries available
Get free access to all sourcing countries identified for this product.
See all countries →See the full supplier coverage for this product
Get free access to all relevant manufacturers, sourcing countries, and product alternatives.
✓ Free for medical industry professionals.
from other manufacturers
from other manufacturers
12 of 80 closest product alternatives
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.
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.
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.
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.
Blackhills Diagnostic Resources, S.L.U. BDR · Spain
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.
CLONIT SRL · Italy
A diagnostic test kit for detecting the MTHFR C677T mutation related to coagulation pathway abnormalities and thrombophilia risk. The kit contains reagents for 32 tests and is available for QiaSymphony SP/AS systems. It is CE Mark certified.
CLONIT SRL · Italy
A diagnostic test kit for detecting the MTHFR A1298C mutation associated with genetic predisposition to thrombophilia. The kit contains reagents for 32 tests and is compatible with QiaSymphony SP/AS extraction systems. It is CE Mark certified.
CLONIT SRL · Italy
A diagnostic test kit for detecting the MTR A2756G mutation associated with genetic predisposition to thrombophilia. The kit contains reagents for 32 tests and is used in cardiovascular disease assessment. It is CE Mark certified.
68 more product alternatives available
Create a free account to compare more product alternatives and supplier options.
© 2026 Suplivia · Home · Browse Products