InviGenius® PLUS

Walk-away DNA/RNA sample preparation

The InviGenius PLUS is a true walk-away system for DNA/RNA extraction and purification from clinical samples – providing a reliable “Sample in – Eluate out” technology!

The combination of well-established magnetic bead based InviMag technology and state-of-the-art process automation allows for standardization and streamlining of
laboratory workflows. Innovative functionality and optimized protocols for demanding samples and applications result in reliable performance and superior DNA and RNA quality for molecular diagnostics*.

New PLUS features

  • Heat lysis and heat elution
  • LIMS connectivity
  • Choice of elution tubes or plates
  • Barcoded labware for complete sample traceability
  • Plug-in for separate hand-held barcode scanner
  • Drop catcher minimizes the risk of cross contamination
  • UV light enables decontamination of the worktable

Starting materials

Whole blood, serum, plasma, urine, stool*, sputum*, BAL, swab, saliva, transport media
*) Sample pretreatment is necessary

Target nucleic acids

genomic DNA, cell-free circulating DNA, RNA & DNA from viruses, bacterial DNA

Fully automated extraction system


InviGenius PLUS deck layout


Sample and reagent loading racks


Separate hand-held barcode scanner


Heat incubator


Waste management

Kits for the InviGenius PLUS

Nucleic acid

Kit

genomic & bacterial DNA, viral DNA/RNA

InviMag Universal Kit/ IG

Virus DNA/RNA

InviMag Virus Midi Kit/ IG
(available from Q1 2017)

genomic DNA

InviMag Blood DNA Mini Kit/ IG (200 µl)

InviMag Blood DNA Maxi Kit/ IG (2 ml)

InviMag SalivaGene DNA Kit/ IG

cell-free, circulating DNA (cfDNA)

InviMag Free Circulating DNA Kit/ IG

Ordering information

Product

Package Size

Catalogue No

InviGenius PLUS

1 unit

5011102000

Sheaths

1000 pieces

5011100200

Sheaths Bundle

10 x 48 pieces/ rack

5011100300

Conductive filter tips, 1100 µl (bundle)

10 x 96 pieces/ rack

5011100400

Waste tray/ IG (disposable)

25 pieces

5011100100

*) In compliance with the Directive 98/79/EC on in vitro diagnostic medical devices (IVD-Directive). Products which are CE-marked according to the IVD-Directive can be used for diagnostic applications in countries where this directive is recognized. The device is not approved by the US FDA.

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