Beckman Coulter Allegra X-30 High-Speed Centrifuge
| Brand | Beckman Coulter |
|---|---|
| Origin | USA |
| Manufacturer | Beckman Coulter, Inc. |
| Type | Benchtop Centrifuge |
| Speed Range | 10,000–30,000 rpm (max 16,000 rpm) |
| Max RCF | 23,511 × g |
| Max Capacity | 4 × 400 mL |
| Dimensions (W × D × H) | 46.0 × 55.0 × 35.5 cm |
| Rotor Compatibility | 13 standard rotors including fixed-angle and swing-bucket configurations |
| Temperature Range | Ambient (4–35 °C) |
| Drive System | Brushless three-phase motor |
| Acceleration/Deceleration Profiles | 10 programmable curves each |
| Timer Range | Up to 9 h 59 min, continuous or short-spin mode |
| Speed Accuracy | ±50 rpm |
| Display | Digital RPM and RCF readout (incremental resolution: 100 rpm) |
| Compliance | FDA-listed, ISO 13485 certified, GLP/GMP-ready with audit trail capability (via optional software) |
Overview
The Beckman Coulter Allegra X-30 High-Speed Centrifuge is an engineered benchtop solution designed for laboratories requiring reliable, high-performance separation of biological samples at elevated rotational speeds. Operating on the principle of sedimentation under centrifugal force, the Allegra X-30 generates up to 23,511 × g at its maximum speed of 16,000 rpm—enabling efficient pelleting of mammalian cells, bacterial cultures, subcellular organelles, and macromolecular complexes. Its compact footprint (46 cm wide) integrates high-capacity throughput (up to 1.6 L total volume with SX4400 swing-bucket rotor) without compromising structural rigidity or thermal stability. The instrument employs a brushless three-phase drive system for low-vibration operation, extended service life, and precise speed control—critical for reproducible separations in regulated environments.
Key Features
- Compact benchtop design (46 × 55 × 35.5 cm) optimized for space-constrained labs while supporting full-scale processing workflows
- Intelligent rotor recognition system prevents overspeeding by automatically detecting installed rotor geometry and enforcing safe operational limits
- Dual-display interface showing real-time RPM and RCF values, with 100-rpm incremental resolution and ±50 rpm speed accuracy
- Programmable acceleration and deceleration profiles (10 each) to minimize sample resuspension and protect shear-sensitive analytes
- Brushless motor architecture delivering consistent torque across speed range, reduced maintenance intervals, and lower acoustic emissions (<65 dBA at 16,000 rpm)
- Integrated safety mechanisms: lid interlock, imbalance detection, automatic rotor brake, and overtemperature protection
- Pre-configured application methods for common formats including 1.5 mL microcentrifuge tubes, PCR strips, and 96-well plates
Sample Compatibility & Compliance
The Allegra X-30 supports a broad spectrum of sample containers and volumes—from 0.2 mL PCR tubes to 400 mL bottles—via 13 interchangeable rotors, including fixed-angle (e.g., F15-8×50y), swing-bucket (e.g., SX4400), and microplate carriers. It accommodates routine clinical and research applications such as whole blood fractionation, cell culture harvest, nucleic acid purification, and virus concentration. From a regulatory standpoint, the instrument complies with ISO 13485:2016 for medical device quality management systems and meets essential requirements under IEC 61010-1 for laboratory equipment safety. When operated with Beckman Coulter’s optional Cytomation™ Software Suite, it supports 21 CFR Part 11-compliant electronic records, user-level access control, and full audit trail functionality—making it suitable for GLP and GMP environments where traceability and data integrity are mandatory.
Software & Data Management
While the Allegra X-30 operates autonomously via its front-panel interface, integration with Beckman Coulter’s Cytomation™ Software enables advanced protocol management, remote monitoring, and secure data export. Protocols—including speed, time, acceleration/deceleration profiles, and temperature setpoints (where applicable)—can be saved, duplicated, and version-controlled. All run logs—including start/stop timestamps, actual vs. set parameters, error codes, and rotor ID—are timestamped and digitally signed. Export options include CSV and PDF formats compatible with LIMS and ELN platforms. Audit trails record operator identity, parameter changes, and system events—fully aligned with FDA expectations for analytical instrument qualification (AIQ) and computerized system validation (CSV).
Applications
- Cell biology: Harvesting adherent and suspension mammalian cells, isolating mitochondria and nuclei
- Clinical diagnostics: Serum/plasma separation from whole blood, preparation of PBMCs
- Molecular biology: Precipitation and pelleting of DNA/RNA, plasmid purification, viral vector concentration
- Microbiology: Bacterial pellet collection for lysate preparation or antibiotic susceptibility testing
- Protein biochemistry: Clarification of cell lysates, isolation of inclusion bodies, membrane fractionation
- High-throughput screening: Processing of 96- and 384-well microplates for assay development
FAQ
What is the maximum relative centrifugal force (RCF) achievable with the Allegra X-30?
The instrument delivers a maximum RCF of 23,511 × g when using the F15-8×50y fixed-angle rotor at 16,000 rpm.
Does the Allegra X-30 support refrigerated operation?
No—the Allegra X-30 is a non-refrigerated centrifuge designed for ambient temperature operation (4–35 °C). For temperature-sensitive applications requiring active cooling, Beckman Coulter recommends the Allegra X-30R variant.
How many rotor types are validated for use with this model?
Thirteen (13) Beckman Coulter–certified rotors are supported, including fixed-angle, swing-bucket, and microplate carriers—each pre-calibrated and registered in the instrument’s firmware.
Is the Allegra X-30 compliant with FDA 21 CFR Part 11?
Yes—when paired with Cytomation™ Software and configured with role-based user accounts, electronic signatures, and immutable audit logging, the system meets core technical requirements for Part 11 compliance.
What safety certifications does the Allegra X-30 hold?
It conforms to IEC 61010-1:2010 for electrical safety, carries CE marking for EU markets, and is listed with the U.S. FDA as a Class II medical device (510(k) cleared).

