Genetic deafness gene detection kit (PCR flow cytometry fluorescence hybridization method)

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.

A molecular diagnostics reagent kit for human CYP2C19 gene typing using PCR with fluorescent probes. The kit supports pharmacogenetic testing for personalized medicine applications.

A gene genotyping detection kit for human MTHFR gene analysis using PCR with fluorescent probe methodology. It enables genetic testing for personalized medicine applications. Available variants: Human MTHFR Gene Genotyping Detection Kit (PCR Fluorescent Probe Method).

A gene genotyping detection kit for human CYP2C19 gene analysis using PCR with fluorescent probe methodology. It supports pharmacogenetic testing for precision medicine applications. Available variants: Human CYP2C19 Gene Genotyping Detection Kit (PCR Fluorescent Probe Method).

PCR-based detection kit for HCMV nucleic acids used in early diagnosis and assessment of fetal, neonatal, and maternal infections. Enables timely clinical management of HCMV-related complications.

A molecular diagnostics reagent kit for human SLCO1B1 and ApoE gene typing using PCR with fluorescent probes. The kit enables genetic analysis for clinical and metabolic assessment.

A diagnostic kit based on GENETRON's proprietary 'one-step method' technology enabling completion of library construction in 1.5 to 3 hours (China patent ZL 201710218529.4). It detects EGFR, KRAS, BRAF, HER2, and PIK3CA gene mutations in DNA and ALK and ROS1 gene fusions in RNA from FFPE tissue samples of non-small cell lung cancer patients, as well as MET gene 14 exon skipping mutations.

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

Genetic testing for hereditary and congenital hearing loss to identify causative variants in deafness-related genes. Supports diagnosis and management of genetic hearing disorders.

Diagnostic test for identifying genetic disorders through molecular analysis of biological samples. The test can detect chromosomal abnormalities and inherited genetic conditions.

Comprehensive testing system for identification of genetic abnormalities and hereditary disorders. Supports clinical diagnosis and prenatal screening applications.

A molecular detection kit for identifying hereditary disease markers and genetic predispositions. Designed for clinical screening and diagnostic purposes in genetic medicine applications.