HUMAN PLACENTA DNA

COT I Human DNA reference material (3 × 500 µg) for molecular biology applications including microarray screening, PCR validation, and quality control. Used as a standard in real-time PCR assays and genomic research protocols.

HCMV DNA liquid standards for molecular diagnostics and quality control in cytomegalovirus testing. These calibrated reference materials enable accurate quantification and validation of CMV DNA detection assays in clinical and research laboratories. Suitable for PCR, qPCR, and nucleic acid amplification method standardization.

Specialized system for maximizing cell-free DNA yield from plasma samples. Optimized for non-invasive prenatal testing and circulating tumor DNA applications.

Nucleic acid purification kit for extracting and isolating DNA/RNA from biological samples in molecular diagnostic workflows. Designed for use with genetic testing, cancer screening, and infectious disease detection assays. Enables downstream nucleic acid analysis including PCR and sequencing applications.

High purity albumin protein extracted from human placenta. This purified protein is used in diagnostic and laboratory applications.

Human blood products and disease-state control plasmas for in vitro diagnostic testing and laboratory quality assurance. These reference materials enable standardization and validation of hematology, immunology, and coagulation assays. Customizable formulations support development, calibration, and performance verification of diagnostic systems.

Integrated platform for molecular diagnostic testing including PCR-based nucleic acid detection systems for infectious disease and genetic testing.

Human tissue and blood-derived materials for in vitro diagnostic development and biomarker research. Available in frozen, fresh, or lyophilized formats as standardized controls, pools, and reference standards for IVD assay validation and quality control testing.

Human control sera for in vitro diagnostics calibration and quality assurance. Provides reference materials for validation of diagnostic assays and laboratory test methods. Produced to specified standards for clinical chemistry and immunodiagnostic applications.

Quality control material for prenatal screening assays across laboratory analyzers. Designed for clinical chemistry and immunology applications with up to 3-year shelf life. Compatible with multiple device platforms including POCT systems for parameters such as NT-proBNP, CK-MB, hsTnI, and AMH.