Parallel capillary electrophoresis system that integrates with robotic arms for high-throughput labs.
- Robotic integration - a custom API and powered drawers offer seamless integration with most laboratory automation systems
- High throughput separations - unattended analysis of more than 2,400 samples every 24 hours
- High separation resolution - resolve a wide range of DNA and RNA fragments. Achieve as low as 3 bp resolution with high sizing accuracy for fragments under 300 bp
- Low cost per sample - choose qualitative or quantitative gel kits that best suit your analysis needs. Realize lower operational costs than other analytical instruments
- Decreased prep time - with room temperature stable reagents and no daily array handling, minimal work is needed to setup runs
- Wide dynamic range - most reagent kits cover approximately two orders of magnitude. High and Standard Sensitivity Kits are available for most applications, extending the overall range of detection
- User-friendly software - automate data scoring. Calculate fragment size and concentration. Create, save, and load customized reports and scoring parameters for flagging and smear analysis
- IQ/OQ services available for use in GMP environments
- Desktop PC supplied with a comprehensive 3-year warranty through HP
The 5400 fragment analyzer system redefines the bounds of nucleic acid QC analysis by using automated parallel capillary electrophoresis. Capable of interfacing with world leading robotic systems, analysis of DNA and RNA samples can now be performed around-the-clock through robotic integration.
The 5400 fragment analyzer system is compatible with all the same high-quality reagent kits available for the 5300 Fragment Analyzer system. Use quantitative kits for analyzing NGS libraries, large fragment smears, genomic DNA, RNA, and small RNA. Additionally, you can use qualitative kits for analyzing PCR amplicons, SSRs/microsatellites, CRISPR generated mutations, or digested DNA.
Caution: For research use only. Not for use in diagnostic procedures.
