This product detects hereditary hypercholesterolemia risk-related genes including LDLR, APOB, PCSK9, LDLRAP1, ABCG5, and ABCG8, and simultaneously screens for drug-related genes SLCO1B1 and APOE to support clinical diagnosis and assessment.
Manufactured by
Cygnus Biosciences (Beijing)Co., Ltd.
China
Cygnus Biosciences was founded by a team from Peking University including Academician Xie Xiaoliang. The company specializes in gene sequencing technology R&D, production and commercialization, with over 100 patents filed in China and internationally. Utilizing proprietary Fluorogenic and ECC error-correction coding sequencing technologies, Cygnus provides gene sequencing platforms and solutions for oncology, microbiology, reproductive health, and food safety applications.
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Randox Laboratories Ltd. · United Kingdom
Diagnostic tests and genetic screening for familial hypercholesterolemia detection. These products support identification and management of inherited lipid disorders.
Nonacus · United Kingdom
A collaborative design NGS panel for familial hypercholesterolemia genetic analysis. Detects pathogenic variants associated with hereditary hypercholesterolemia. Available as a pre-designed panel for rapid implementation in germline testing.
Origin Biotechnology Co., Ltd. · Taiwan
A molecular detection kit for identifying hereditary disease markers and genetic predispositions. Designed for clinical screening and diagnostic purposes in genetic medicine applications.
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