Automated DNA & RNA 

Extraction System


The abGenix™ is a mid throughput system for automated nucleic acid extraction. It offers the flexibility to simultaneously process 1-32 samples per run, meeting your sample processing requirement.

Redefining extraction



abGenix™ comes with user friendly software; saving time and labour

Rapid Extraction

Streamline your work process

Reliable System

With cost effective and affordable kits for various kind of samples

High quality nucleic acid extraction

Using Magnetic Pillar Rod Technology

Small footprint

Fits easily on lab bench top

abGenix 100118

Product Details

Technical Specification

Catalogue No.800800
Extraction MethodMagnetic pillar rod technology
Capacity1- 32 samples per batch
Processing time30- 60 mins (Kit dependent)
Processing volumeFixed volume: 100- 200µl (Kit dependent)
Elution volumeFixed volume: 60- 100µl (Kit dependent)
Collection efficiency of magnetic particles>95% depending on sample and reagent kit
Heating temperatureRoom temperature to 120°C
Contamination controlUV light
Hardware• Integrated microprocessor, no external PC required
• Touch control panel
• Tablet pairing and control
Operation interfaceEnglish/ Chinese language operating system
Protocols15 pre-installed protocol in instrument, unlimited in tablet
Dimension (W x D x H)440mm x 420mm x 440mm
Net weight31.5kg
Power usageAC 100- 240V, 50/ 60Hz
Power consumption600VA
Operational ambient temperature10- 40°C

Order Information

Cat. NoProductProduct Description
800800abGenix™ Automated DNA & RNA Extraction SystemMagnetic pillar automated system for extraction of DNA/ RNA, up to 32 samples per run. Tablet included.
800850abGenix™ Strip Reagent AdapterAdapter to hold the pre-filled strip reagents. Holds up to 8 reagent strips.
800851abGenix™ Mixing SleevesMixing sleeves
800853abGenix™ Magnetic BaseMagnetic base for standard 96-well plates and abGenix™ extraction plates.

For more information, please call (65) 6778 6822 or email

No, the mixing sleeve is sterilized by ethylene oxide and is disposable.

No, autoclaving it may affect the structure of the adapter. We recommend using disinfector such as hypochloric acid or ethyl alcohol to do sterilization.

850µl, i.e. without solution splashing out during mixing.

Yes, you can connect 2 tablets to one instrument and both tablets are able to control the abGenix™.

The UV light will stop when the instrument door is opened. abGenix™ will continue with the UV disinfection upon closing the instrument door again.

The window of experiment cabin door is tinted for UV protection. It is possible to have normal LED lighting but it requires rewiring and assembly.

Its lifespan ranges from 3 to 5 years depending on the usage frequency. It is recommended to replace the UV light bulb when the UV intensity is lower than 70µW/cm.

The abGenix™ can be placed inside a biosafety cabinet, but since the instrument may shake within a certain range, it is necessary to strengthen the biosafety cabinet. The exterior is not resistant to UV light.

Yes, by utilizing the adapter, both strips and plate can be used concurrently in a run.

The abGenix™ will prompt a message allowing the operator to choose between continuing or ending the experiment run after power has resumed.

No, the elution volume is fixed due to the pre-filled condition of the cartridges.

It is not recommended to reduce the volume any lower than 60µl, which is required for proper mixing. Furthermore, results are not guaranteed.

Yes, the protocol is optimized that way.

The temperature in the manual is the optimum performance parameter. This has been done many times without the viral RNA degrading. It is not recommended to change the temperature parameter.

All our elution buffer are made without EDTA.

Size of the beads may differ for each kit and have different binding capacity.

Due to reagent drops hanging on and liquid residues on foil film, the actual measured elution buffer volume may be less than 60µl or 100µl. PCR result will not be affected should the difference be within 10µl. Also, if the difference between start volume and final volume is within 20µl, the PCR reaction should work just as well. This difference is mainly caused by evaporation during the extraction process.

The lysis temperature in the protocol is referring to the heating block temperature; the actual temperature of the place will not exceed 60°C.