An expanded synthetic biology platform enables the assembly of long, high-complexity DNA sequences, reducing technical barriers and supporting next-generation research in medicine, vaccines, and agriculture.

A low DNA binding consumables range minimizes interactions between nucleic acids and plastic surfaces, supporting more reliable NGS library preparation.

A redesigned 1.6 mL storage tube minimizes dead volume near the base to improve sample recovery while maintaining pipette access.

New validated automated workflows enable higher-throughput, more reproducible NGS library preparation using on-deck fragmentation, ligation, and auto-normalization.

An extraction-free kit enables gene expression analysis directly from hepatocyte lysates, delivering results in 75 minutes with sensitivity comparable to RNA purification.

Researchers are using long-read whole-genome sequencing as a first-line test to study sudden unexplained death in childhood, pairing each child’s genome with parental data to detect complex variants and clarify inherited and de novo risk.