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This single test interrogates over 500 genes to profile a patient’s solid tumor, helping to increase the likelihood of identifying an immuno-oncology biomarker or clinically actionable biomarkers that enable targeted therapy options or clinical trial enrollment.

Scientists need to be aware of many factors to build accurate and reproducible serial dilution protocols. 

The Zymo-Seq™ SPLAT DNA Library Kit employs SPlinted Ligation Adapter Tagging (SPLAT) technology, a unique method that directly ligates adapters onto single-stranded DNA fragments.

Nanopore sequencing platforms provide researchers the freedom to rapidly sequence long microbial nucleic acid fragments in the field. 

The Quick-DNA/RNA™ Water Kit is designed to provide researchers with the tools they need to achieve superior results in a variety of applications, from pathogen surveillance to environmental monitoring. 

Nonviral genetic engineering methods for improved cancer immunotherapy

The new CellDrop FLi launch includes enhanced hardware for improved cell counting performance, along with six new cell counting applications including fixed samples, hepatocytes and Erythrosin B

Optimizing nonviral genetic engineering of resting T cells for improved cancer immunotherapy

A modern take on supercritical fluid chromatography separates fact from fiction.

Assay Automation Makes Cutting-Edge Research More Accessible to Labs

Liquid chromatography-mass spectrometry allows scientists to accurately assess the quantity and quality of synthesized oligonucleotides. 

It makes it easy to consolidate and analyze bioprocess data in one central location, helping to solve the puzzle and transfer data to insights. 

A streamlined protocol for generating iNK cells from PSC spheroids

This new initiative aims to empower scientists around the world with cuttingedge RNA sequencing (RNA-Seq) technologies to explore the transcriptome of ANY organism.

The Sapio Partner Program ensures services partners are certified in the deployment and support of Sapio's lab informatics platform.

Expansion of metabolite identification database accelerates insights, translation of findings for small molecule biomarker studies

Discover how researchers expand their understanding of neurological disorders by using cytometry by time of flight (CyTOF) analysis. 

A robust platform for analyzing 3D genome architecture and epigenomic features enables a deeper understanding of gene regulation in specific cell types.

Explore a cfDNA library preparation workflow that provides high yield and conversion to improve sensitivity and detection of low variant allele frequencies (VAF).