WOLF® G2 Cell Sorter
NanoCellectGentle Sorting. Healthy Cells. Better Science.
Gentle Sorting. Healthy Cells. Better Science.
A module for the WOLF ® G2 Cell Sorter to provide cooling and stirring of sample.
QIAseq FastSelect: Increase your unique reads, discover more biology
QIAseq FastSelect: Increase your unique reads, discover more biology
VisualAIâ„¢, an add-on module for VisualSpreadsheet 6, is a pre-trained, AI-driven image analysis module that recognizes images of biopharmaceutical aggregates captured on any FlowCam 8100 or FlowCam LO instrument. VisualAI is a powerful tool for quantifying protein aggregate and silicone oil droplet content in protein-based drug products.
BioData Solutions® offers bioanalytical consulting for Operational Program Management, Validation, Method Development, Data Review and Analysis, Market Planning for modalities from small molecule to cell and gene therapies.Â
Ariadne Software®, a brand of BioData Solutions®, offers automation software for bioanalytical auditing of small and large molecule pharmacokinetic data as well as cut point and sensitivity determination for ADA data.Â
First IHC companion diagnostic for determining folate receptor alpha (FOLR1) protein expression in EOC patients who may benefit from ELAHEREâ„¢ (mirvetuximab soravtansine)

The Luminex xMAP INTELLIFLEX is an advanced platform for accurate protein measurement in a compact instrument. With an option for a second reporter laser, it allows detection of two parameters on a single bead, maximizing data points and sample processing. Designed for high throughput, it is the most advanced Luminex instrument. Compatible with R&D Systems Luminex assays and Quantist Analysis Software.
The FLEXMAP 3D is a versatile and powerful multiplexing platform from Luminex. Fast read time, compatibility with 96- and 384-well plates, and ease of integration with front-end automation systems make the FLEXMAP 3D a reliable choice for high-throughput applications. Â Compatible with R&D Systems Luminex assays and Quantist Analysis Software.
The Luminex 200 utilizes principles of flow cytometry and is the gold standard for basic multiplexing protein needs. Simultaneously multiplex up to 100 analytes in a single microplate well. Delivers fast and cost-effective results on many assay formats. The Compatible with all R&D Systems Luminex assays and the Quantist Analysis Software.
Fully automatic tube laser marker.
Easy-to-use, accessible benchtop single-molecule protein sequencing platform that empowers any lab, anywhere to obtain critical proteomic insights quickly and efficiently from the convenience of your lab, no expertise or infrastructure required.
The Twist 96-Plex Library Preparation kit enables high-throughput library construction for whole genome sequencing.Â
The Twist Alliance CeGaT RNA Fusion Panel is a targeted RNA sequencing solution designed to detect both known and novel gene fusions across 160 genes associated with over 30 cancer types, enhancing cancer and precision medicine research.
Twist Exome 2.0 is a comprehensive exome sequencing panel designed to detect rare and inherited diseases, as well as germline cancers. Its high uniformity and low off-target rate deliver best-in-class sequencing efficiency, enabling quality data collection with less sequencing.
For best-in-class results, use best-in-class tools
Delivers excellent uniformity and increased on-target rates
The Twist Standard Hybridization Reagent Kit v2 is the gold standard for efficient and specific binding of panel probes to your regions of interest. Coupled with Twist’s Catalog or Custom Panels, this standard hybridization workflow provides the optimal conditions for a broad range of content.
Enables sequencing of genes that are difficult or impossible to fully sequence with short read technology.Â
Focus on important genes in pharmacogenomics that are critical to drug metabolism and patient therapeutic response.
Twist Diversity SNP Panel gives researchers a new flexible ethnicity-neutral gold standard to use for GBS
Deep coverage of clinically focused targets that allow for the study of methylation patterns that may be relevant to early cancer detection and diagnosis from tumor and liquid biopsy samples.