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Illumina develops, manufactures and markets integrated systems for the analysis of genetic variations and biological functions. The company also provides sequencing and array-based solutions for genetic analysis, as well as genotyping, NIPT and whole-genome sequencing services for government laboratories, hospitals, an ...
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Covid-19 Illumina

Clinical Laboratory

SARS-CoV-2 (COVID-19) Test
Illumina COVIDSeq Test

The Illumina COVIDSeq Test is the first NGS test approved for use under the US Food and Drug Administration’s Emergency Use Authorization (EUA). This amplicon-based NGS test includes 2019-nCoV primers designed to detect RNA from the SARS-CoV-2 virus in nasopharyngeal, oropharyngeal, and mid-turbinate nasal swabs from patients with signs and symptoms of infection who are suspected of COVID-19. The test can be run on the Illumina NovaSeq 6000 Sequencing System, NextSeq 500 Sequencing System, NextSeq 550 Sequencing System, or NextSeq 550Dx Instrument.
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About Illumina

Illumina develops, manufactures and markets integrated systems for the analysis of genetic variations and biological functions. The company also provides sequencing and array-based solutions for genetic analysis, as well as genotyping, NIPT and whole-genome sequencing services for government laboratories, hospitals, and reference laboratories, among others.
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NGS System

NGS System

Model: NextSeq 550Dx
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Description:

The NextSeq 550Dx is a FDA-regulated and CE-IVD marked next-generation sequencing (NGS) system with dual boot functionality, and includes a diagnostic mode (Dx mode) and a research mode, providing the flexibility to perform both clinical research and develop a range of IVD assays on a single instrument.
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Full Description Specifications

Description

The NextSeq 550Dx is a FDA-regulated and CE-IVD marked next-generation sequencing (NGS) system with dual boot functionality, and includes a diagnostic mode (Dx mode) and a research mode, providing the flexibility to perform both clinical research and develop a range of IVD assays on a single instrument. It offers a validated high-throughput platform for large clinical laboratories, and fully-integrated onboard analysis software with modular software architecture to support current and future assays. Request Information

Specifications

• Instrument configuration RFID tracking for consumables
• Instrument control computer Processor: Dual Intel® Xeon® E5-2648L v3
1.8 GHz CPU, Memory: 128 GB
Hard Drive, Dx Mode: 2  2 TB (RAID 1)
Hard Drive, Research Mode: 2  2 TB (RAID 1)
Operating System: Windows 10
• Operating environment Temperature: 19°C to 25°C (22°C ± 3°C)
Humidity: Noncondensing 20%–80% relative humidity
Altitude: 0-2000 m (6500 ft)
Ventilation: Up to 2048 BTU/hr @ 600 W
For Indoor Use Only
• Light emitting diode (LED) 520 nm, 650 nm; Laser diode: 780 nm, Class IIIb
• Dimensions W × D × H: 54 cm × 69 cm × 58 cm
Weight: 186 lbs, Crated Weight: 360 lbs
• Power requirements 100–120 VAC 15 A, 220–240 VAC 10 A
• Radio frequency identifier (RFID) Frequency: 13.56 MHz
Power: Supply current 120 mA, RF output power 200 mW
• Product safety and compliance NRTL certified IEC
61010-1 CE marked
FCC/IC approved Request Information

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