MT-Prep™ 24
Full automation for everyday sample purification
With a small footprint, it is the perfect partner for laboratories with limited bench space and flexible medium throughput sample processing.
Total processing time (24 samples):
55 mins
Total hands-on time:
10 mins
Features & Benefits
- Minimise errors and contamination with full automation
- Flexible throughput — process between 1 to 24 samples with no reagent and plastics waste
- Minimum maintenance requirements mean maximum productivity
- Purify RNA or DNA from up to 24 samples in 55 minutes
- Sample and reagent traceability
Maximum convenience and versatility
Process between 1 to 24 samples without reagent or plastic waste. Pre-packaged reagent cassettes and reaction chambers are merged for quick and easy setup, whilst sample racks can be easily removed to also serve as convenient carriers. With the flexible throughput options, and ready-to-use reagents, achieve high quality sample purification with maximum convenience.
Uniquely designed for better performance
With proven liquid handling technology, the MT-Prep™ 24 is engineered with advanced motor controls and features a unique reaction chamber design delivering unrivalled mixing ability. The result is high-yield and high-purity nucleic acid extraction with elevated lysis and elution efficiencies and minimal magnetic bead and alcohol residues in the final eluate. Consistently obtain high purity and high yield nucleic acids for the next stage of your workflow.
True walk-away efficiency
Full sample extraction is performed in only 55 minutes, allowing minimal turnaround times, and freeing up time to conduct other critical work. Setup is easy and intuitive with the user-friendly user interface. Customised magnetic bead separation technology that eliminates tip congestion, combined with the sample traceability system allows minimal hands-on time which prevents inherent handling errors.
Virtual Demo
Explore the MT-Prep™ 24
System Specifications
MT-Prep 24™ System is intended for in vitro diagnostics use by authorised clinical testing laboratories in Australia, and the European Economic Area and is included on the Australian Register of Therapeutic Goods (ARTG), and compliant with the European IVD Directive 98/79/EC.
