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NovoCyte benchtop flow cytometer system, designed for all types of laboratories
Instrument control and data acquisition software for GC/MSD, GC/TQ, and GC/Q-TOF
Incorporate new and emerging biomarkers for tumor genomic profiling with custom cancer NGS panels
Fully automated, rapid, sample-to-report CGP solution for hematologic malignancies
Advanced technology for sensitive DNA variant detection with a streamlined workflow
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The NovoCyte Opteon spectral flow cytometer, with up to 5 lasers, is designed to further your flow cytometry research.
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NovoCyte Advanteon with 1- 3 laser options, up to 21 fluorescence channels, 23 independent detectors
Bond Elut 96 round-well plates support well-plate SPE applications with smaller sample volumes.
Comprehensive GPC/SEC software for GPC/SEC instrument control, data acquisition, and analysis
Comprehensive genomic profiling of solid tumors to detect key classes of somatic alterations.
SPEC disk SPE delivers superior flow characteristics and trouble-free automation.
TOP-DNA enables good recovery of high-purity synthetic DNA oligonucleotides.
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Have the flexibility to choose from up to 30 fluorescence channels utilizing up to 5 lasers.
Bond Elut Lipid Extraction SPE 1 mL cartridges and 2 mL 96-well plates provide highly selective and efficient extraction of lipids for lipid analysis, lipid profiling, and lipidomics workflows.
Provides cost efficient and flexible analysis beyond flame atomic absorption
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Parallel capillary electrophoresis system for ultra-high-throughput labs with robotic integration.
Achieve trace-level analysis of volatile and semi-volatile organic compounds.
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Satisfies all your automated multiangle reflectance and transmission spectrophotometer needs.
DNA library prep solutions with hybrid capture-based target enrichment for complex libraries
|SureSelectXT Reagent Kits enable post-capture pooling of enriched, sequencing-ready libraries. The kits are compatible with FFPE samples and high-quality libraries can be generated from 3 μg DNA input or lower 200 ng input. This kit provides high-complexity libraries for rare allele detection.