3500 Dx Genetic Analyzer by Thermo Fisher Scientific Invitrogen
Manufacturer Thermo Fisher Scientific Invitrogen
The 3500 Dx Genetic Analyzer CS2 is the latest addition to our family of Applied Biosystems® genetic analyzers based on capillary electrophoresis. The 3500 Dx Genetic Analyzer CS2 is an IVD-labeled instrument, making it the first Sanger sequencing platform cleared for sequencing analysis of DNA.
Designed with you in mind, the 3500 Dx Genetic Analyzer CS2 gives you automated operation, easy-to-install consumables, electronic tracking of instrument performance and maintenance tasks, and integrate... Read more
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3500 Dx Genetic Analyzer
The 3500 Dx Genetic Analyzer CS2 is the latest addition to our family of Applied Biosystems® genetic analyzers based on capillary electrophoresis. The 3500 Dx Genetic Analyzer CS2 is an IVD-labeled instrument, making it the first Sanger sequencing platform cleared for sequencing analysis of DNA.
Designed with you in mind, the 3500 Dx Genetic Analyzer CS2 gives you automated operation, easy-to-install consumables, electronic tracking of instrument performance and maintenance tasks, and integrated analysis software—so you can focus on the outcome.
You can run the instrument in either IVD mode (for diagnostic HLA typing by SeCore® HLA typing kits) or RUO mode to develop other applications, including de novo sequencing and resequencing, as well microsatellite analysis, MLPA®, LOH, MLST, and SNP confirmation or screening and fragment analysis.
Features & Benefits:
Designed with you in mind, the 3500 Dx Genetic Analyzer CS2 gives you automated operation, easy-to-install consumables, electronic tracking of instrument performance and maintenance tasks, and integrated analysis software—so you can focus on the outcome.
You can run the instrument in either IVD mode (for diagnostic HLA typing by SeCore® HLA typing kits) or RUO mode to develop other applications, including de novo sequencing and resequencing, as well microsatellite analysis, MLPA®, LOH, MLST, and SNP confirmation or screening and fragment analysis.
Features & Benefits:
- The 3500 Dx Genetic Analyzer CS2 is an IVD-labeled platform for Sequencing-Based Typing using SeCore® HLA typing kits. Sanger sequencing is known as the "gold-standard" for its accuracy, reliability, and ease of use. It is also used for confirmatory sequencing by clinical labs.
- High accuracy: 99% concordance as shown in clinical trials using SeCore® HLA typing kits
- Proven through decades of results—including sequencing of the first human genome—Applied Biosystems® genetic analysis systems are trusted standards for Sanger sequencing.
Reduced instrument hands-on time with simplified installation and removal of consumables and accessories - Controlled and efficient run setup with intuitive user interface, preconfigured plate templates, and software-controlled functions (plate setup, data collection, analysis)
- Instrument run-times as short as 1 hour; sample-to-result in as little as 1.5 days
- Maintenance calendar with programmable prompts and service history
- Security and electronic signature, RFID (radio frequency identification) tracking of consumables, built-in quality controls, and real-time data quality evaluation
Collect data in either IVD (diagnostic for HLA typing) or RUO mode - Develop other applications in RUO mode, including de novo sequencing and re-sequencing, as well as fragment analysis applications such as microsatellite analysis, MLPA®, LOH, MLST, and SNP confirmation or screening
- Partner with Life Technologies to develop assays for FDA submission
- Different configurations to meet your throughput needs: 8-capillary (3500 Dx) and 24-capillary (3500xL Dx) versions
Product Overview
3500 Dx Genetic Analyzer
Manufacturer Thermo Fisher Scientific Invitrogen
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