Biomek  i5 Span 8 NGS Workstation for Illumina TruSight Tumor Panels Enclosed

C23346


The Biomek i5 Span 8 NGS Workstation configured specifically for Illumina's TruSight Panel assays such as Trusight Tumore 170. The 25 deck positions, Span 8 pipetting pipetting and on-line 360 gripper enable flexibility and efficiency for processing a full or partial kit and helps reduce the required dead-volume. Standard on-deck process control elements such as shakers, peltiers and optional thermocyclers, enable significant reductions in hands-on time while also increasing throughput, productivity, efficiency. The industry leading Biomek software provides technology that enables Beckman Application Scientists and customers to create simple, yet comprehensive methods with unmatched intelligence and flexibility. A repository of demonstrated1 (definition of demonstrated as a footnote on the page) NGS methods (hyperlink italicized text to Demonstrated Biomek Methods Card) is available. Each method comes standard with intuitive User Interfaces and tools like Deck Optix(TM) (hyperlink to Deck Optix) to better ensure accurate setup and reduce costly errors.

Especificações

Minimum Table Support Requirements #N/A / #N/A
Platform Biomek i5 Span 8 Enclosed
Pod and Tool Type Span-8
Installation Category II
Power Requirements 100-240 VAC, 10 A, 50/60 Hz
Operating System Windows® 10
Software Biomek Method Launcher, Biomek PowerPack software, Biomek software, DART 2.0 software, SAMI EX scheduling software
Display 22" controller screen
Operating Mode(s) Semi-automated, manual, controlled by operator
Autoclavable No
Material(s) ABS Cover, Acrylic panels, Aluminum chassis
Finish Hardcoat anodized coating, High-gloss paint
Weight 172 kg / 379.2 lb
Width 112 cm / 44.1 in
Depth 81 cm / 31.9 in
Height 112 cm / 44.1 in
Package Quantity 1
Temperature Range 10° C - 30°C
Humidity Restrictions 20%–85% (non-condensing) at 30°C

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The listed regulatory status for products correspond to one of the below:
IVD: In Vitro Diagnostic Products. These products are labeled "For In Vitro Diagnostic Use."
ASR: Analyte Specific Reagents. These reagents are labeled "Analyte Specific Reagents. Analytical and performance characteristics are not established."
CE: Products intended for in vitro diagnostic use and conforming to European Directive (98/79/EC). (Note: Devices may be CE marked to other directives than (98/79/EC)
RUO: Research Use Only. These products are labeled "For Research Use Only. Not for use in diagnostic procedures."
LUO: Laboratory Use Only. These products are labeled "For Laboratory Use Only."
No Regulatory Status: Non-Medical Device or non-regulated articles. Not for use in diagnostic or therapeutic procedures.