Human genetics

Human genetics PCR kits provide precise and sensitive tools for detecting genetic variations, mutations, and polymorphisms associated with inherited diseases, cancer predisposition, pharmacogenetics, and other clinical conditions. Accurate genetic testing supports personalized medicine, risk assessment, and targeted therapies.
These kits, based on real-time PCR technology, enable reliable detection of single nucleotide polymorphisms (SNPs), insertions/deletions, and gene rearrangements in human genomic DNA. These PCR assays deliver accurate and reproducible results in routine and specialized laboratory workflows. Available in CE IVD-marked formats for diagnostic use and research use only (RUO) versions, applications include hereditary cancer panels (e.g., BRCA1/2), thrombophilia testing (e.g., F2, F5), detection of CML (chronic myelogenous leukemia) associated with M-bcr-abl chromosomal rearrangement, pharmacogenetics, and other genetic markers from clinical samples.