Thermo Fisher Scientific
Instrument
The Applied Biosystems™ 3500 Series Genetic Analyzers are specifically designed to support the demanding performance needs of validated and regulated environments while retaining the unsurpassed application versatility that life science researchers expect. The 8-capillary 3500 Genetic Analyzers continue to set the standard in capillary electrophoresis.
– Number of capillaries: 8 capillaries
– Compatible capillary length: 36 cm or 50 cm
– Number of fluorescent dyes: 6 colors
– Capacity: 2 plates, compatible with 96-well plates or 8-tube strips
– Compatible with dye sets: E, Z, F, E5, D, G5, J6, J6-T
– Polymer: POP-4™, POP-6™, POP-7™
‘- Sample throughput: ≥368 samples/day for sequencing, ≥1104 for fragment analysis
‘- Average read length in 90% of samples ≥ 850 bases
– Minimum run time: ≤30 minutes
– Dimensions: 61 cm x 61 cm (122 cm open) x 72 cm (LxWxH)
– Weight: 82 kg
– Operating conditions:
+ Temperature 15°C–30°C
+ Humidity: 20-80%
+ Power supply: 100–240V (±10%); 50–60 Hz (±10%)
+ Electrophoresis voltage: Up to 20 kV”
The Applied Biosystems SeqStudio 8 Flex Genetic Analyzer offers design improvements and technological advances to the capillary electrophoresis (CE) workflow. It delivers gold-standard Sanger sequencing and fragment analysis data quality with increased flexibility, easier operation, and cloud connectivity to enable researchers to manage their workloads and work/life balance effectively. Designed for ultimate ease-of-use, this mid-throughput system offers high quality, excellent reliability, and an optimal user experience for researchers who want to work smarter in the lab.
The Applied Biosystems™ 3500 Series Genetic Analyzers are specifically designed to support the demanding performance needs of validated and regulated environments while retaining the unsurpassed application versatility that life science researchers expect. The 24-capillary 3500xL Genetic Analyzers continue to set the standard in capillary electrophoresis.
The 3500xL Genetic Analyzer is a 24-capillary sequencing platform that can be used for a wide variety of applications, including de novo sequencing and resequencing (mutational profiling), as well as microsatellite analysis, MLPA™, LOH, MLST, and SNP validation or screening. The majority of applications can be run on a single polymer and capillary array.
Through evolution and innovation, the EmbryoMap solution has been analytically validated for detection of whole- and sub-chromosomal imbalances with highly reproducible copy-number, using cell line reference material and embryo biopsy samples
Samples are prepared for sequencing using the EmbryoMap Sample Prep Kit, sequenced on the Illumina MiSeq Sequencing System and data analysis and reporting performed using eMap software
The QuantStudio™ 12K Flex system is a highly flexible, comprehensive real-time PCR platform that leverages the best of Applied Biosystems real-time technology in a single instrument. The QuantStudio™ 12K Flex Real-Time PCR System includes easy-to-change blocks that can accommodate OpenArray® plates, TaqMan® array cards, 384-well, 96-well, and FAST 96-well plates allowing you to select the format that is right for your project whether it’s now or in the future, for maximum flexibility and consistency in your research.
Thermo Fisher Cloud
Thermo Fisher Cloud provides scientists with a secure place to store, analyze, and share data. Applied Biosystems qPCR Analysis Modules within the Thermo Fisher Cloud are web browser-based software tools that are flexible, fast and easy to use. These software tools are compatible with Mac or PC as well as most Applied Biosystems instrument file types.
The QuantStudio™ 12K Flex System’s intuitive software, easy touch screen setup, automation integration, effortless block exchange, and easy-to- use OpenArray® components are designed to let you get started right away and reduce hands on time. Plan for the future and save time, money, and space in your lab with the only all-in-one qPCR instrument enabling a broad range of applications with maximum throughput.
• Consolidated Workflow: DNA denaturation and bisulfite conversion process in one step.
• High Yield: Desulfonation and purification on a spin-column allows elution of bisulfite-converted DNA in as little as 10 µl.
• Suitable for Various Downstream Applications: Bisulfite-converted DNA can be robustly PCR amplified for downstream analyses including endonuclease digestion, sequencing, microarrays, etc.
NovaSeq X also significantly reduces waste and environmental impact, reflecting Illumina’s commitment to using its technology to support the health of people and the planet. NovaSeq X features a 90% reduction in packaging waste and weight and 50% reduction in plastic usage compared to NovaSeq 6000.
Model: Basic Yellow
Manufacturer: Lynn Peavey
Origin: United States