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Guidelines for correct operation and avoiding hazards.
Precautions related to electrical power and connections.
Recommended operating conditions and environmental considerations.
Handling of biological samples and infectious agents.
Safety measures when handling chemicals used with the instrument.
Procedures for safe collection and disposal of waste.
Warnings and precautions regarding moving parts and mechanical risks.
Information on potential heat-related risks from instrument components.
Glossary of safety warning terms in multiple languages.
Explanation of safety symbols and their meanings.
Overview of the manual's structure and content.
Details on technical assistance, policy, and version management.
Description of the instrument's purpose and target users.
Explanation of the automated sample preparation workflow.
Identification and description of the instrument's external components.
Identification and description of the instrument's internal components.
Site, power, and environmental prerequisites for installation.
Instructions for connecting the instrument to electrical power.
Steps for safely removing the instrument from its packaging.
Procedures for setting up the instrument after unpacking.
Instructions for safely packaging the instrument for transport.
Description of the software interface and button functions.
Step-by-step guide for starting and executing protocols.
Instructions for loading reagent bottles, tip racks, and samples.
Procedures for managing protocols on the instrument.
How to save run reports, log files, and other data.
Accessing system information and software versions.
How to use the shaker function independently.
How to use the centrifuge function independently.
Recommended disinfectants and detergents for cleaning.
Procedures for disinfecting instrument surfaces and components.
Steps for removing RNase contamination.
Steps for removing nucleic acid contamination.
Routine tasks after each protocol run.
Tasks to perform at the end of each day.
Tasks to perform on a monthly basis.
Tasks performed as needed or at least every six months.
Specific procedures for cleaning after a plastic crash event.
Information needed to report an error effectively.
Guide to identifying and resolving instrument errors.
Specifications and performance details of the instrument.
Operating and storage conditions for the QIAcube.
Recommended conditions for storing the instrument.
Physical dimensions and key hardware specifications.
Information on proper disposal of electronic waste.
Regulatory compliance statement regarding FCC regulations.
Statement of compliance with European directives.
Diagrams showing correct sample loading for the centrifuge and shaker.
List of available accessories and their catalog numbers.
Legal terms and conditions regarding warranty and liability.
| Automation | Fully automated |
|---|---|
| Interface | Touchscreen |
| Elution Volume | 50-200 µl |
| Processing Time | 30-60 minutes per run |
| Operating Temperature | 15-30°C |
| Humidity Range | 20-80% non-condensing |
| Sample Type | DNA, RNA, protein |
| Capacity | 12 samples per run |
| Power Supply | 100-240 V AC, 50-60 Hz |
| Compatibility | QIAGEN spin-column kits |
| Throughput | Up to 12 samples per run |






