← Back to Browse
ProductDiagnostic Tests

Genvinset® HFE S65C

Zaragoza, 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.

Manufactured by

Zaragoza, Spain

As a biotechnology company, BDR is focused on researching, developing, producing and selling in vitro diagnostic products for human diagnostics (CE-IVD). BDR is specialized in Real Time PCR (qPCR), fragment analysis (QF-PCR) and NGS technologies, apart from having its own bioinformatics department in charge of the development of specific software for the analysis of results. Our quality system complies with the most demanding international standards. We have all the required certifications for European manufacturers (UNE-EN-ISO 13485, CE certification, compliance with the European Directive 98/79/CE). In addition, our continuous improvement program includes the yearly participation in External Quality Assessments (EQAs) through different international entities, always obtaining a high score.

✦ Product-Specific Coverage

AI supplier coverage for this product

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.

37
Relevant manufacturers
matched to this product
95
Relevant products analyzed
for supplier coverage
14
Sourcing countries
identified

AI-Matched Alternative Products

from other manufacturers

AI-Matched Alternative Products

from other manufacturers

12 of 95 closest product alternatives

95 products

Haemochromatosis - S65C

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.

View Details

Hemochromatosis Mutations Kit RQ

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.

View Details

HFE Hemochromatosis Genetic Test Kit

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.

View Details

Haemochromatosis - H63D

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.

View Details

RealQuality RS-HEMO H63D

AB ANALITICA Srl · Italy

A molecular diagnostic test for HFE gene H63D mutation detection. This test is used in hemochromatosis genetic assessment.

View Details

RealQuality RS-HEMO C282Y

AB ANALITICA Srl · Italy

A molecular diagnostic test for HFE gene C282Y mutation detection. This test is used in hemochromatosis screening and genetic assessment.

View Details

Attomol Haemochromatosis Realtime TM 2

Attomol GmbH - Molekulare Diagnostika · Germany

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.

View Details

Haemochromatosis - C282Y

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.

View Details

Human MTHFR Gene Typing Detection Reagent Kit (PCR-Fluorescent Probe Method)

Coyote Bioscience Co.,Ltd · China

A molecular diagnostics reagent kit for human MTHFR gene typing using PCR with fluorescent probes. The kit enables genetic analysis for clinical and personalized medicine applications.

View Details

Attomol Hämochromatose-Duplex Realtime LT

Attomol GmbH - Molekulare Diagnostika · Germany

Real-time PCR diagnostic test kit for simultaneous detection of hemochromatosis mutations C282Y and H63D. Available with 20 or 100 determinations.

View Details

gb GENETIC LACTO

GENERI BIOTECH s.r.o. · Czech Republic

CE IVD real-time PCR kit for detection of genetic polymorphisms and mutations in human genomic DNA using fluorescently labelled probes. Enables genotyping of pharmacogenetic variants including CYP2C19, TPMT, UGT1A1, and alpha-1 antitrypsin mutations for personalized medicine applications.

View Details

Genetic Disease Screening Kit

Axbio (shenzhen) Co.,LTD · China

Diagnostic test kit for identification of genetic mutations and inherited disorders through nucleic acid sequencing. Supports clinical genetic testing and carrier screening applications.

View Details

83 more product alternatives available

Create a free account to compare more product alternatives and supplier options.

Get Free Access →

© 2026 Suplivia · Home · Browse Products