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Centurion Scientific K1015 Benchtop High-Speed Centrifuge

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Brand Centurion Scientific
Origin United Kingdom
Model K1015
Instrument Type Benchtop Centrifuge
Speed Range 500–15,000 rpm
Max RCF 22,000 × g
Max Capacity 8 × 50 mL
Acceleration/Deceleration 10-step programmable
Timer Range 0–9999 min (1-sec increment)
Noise Level <60 dB(A)
Dimensions 23 × 23 × 35 cm
Weight 13 kg (without rotor)
Power 140 W
Rotor Compatibility Multiple fixed-angle and swing-out rotors including BRK5424, BRK5436, BRK5448, BRK5494, BRK5407, BRK5408, BRK5401, BRK5508S
Safety Features Four-point lid lock, auto-rebalancing vibration detection, lid interlock sensor, overspeed protection, motor overheat sensor
Chamber Material Stainless steel
Drive System European-sourced brushless DC motor

Overview

The Centurion Scientific K1015 is a compact, high-performance benchtop centrifuge engineered for precision separation of biological macromolecules—including proteins, nucleic acids, subcellular organelles, and viral particles—in research, clinical diagnostics, and quality control laboratories. Operating on the principle of sedimentation under controlled gravitational force (RCF), the K1015 delivers reproducible, high-resolution separations across a wide operational range (500–15,000 rpm; up to 22,000 × g). Its compact footprint (23 × 23 × 35 cm) and lightweight design (13 kg without rotor) make it ideal for space-constrained environments such as biosafety cabinets, laminar flow hoods, or shared core facilities—without compromising mechanical stability or thermal management.

Key Features

  • Intuitive 4.3-inch LCD touchscreen interface with multilingual support and real-time parameter display (rpm, RCF, time remaining, temperature estimation)
  • 10-step programmable acceleration and deceleration profiles to minimize sample disturbance during pelleting or gradient formation
  • 108 user-programmable protocols stored in non-volatile memory, supporting GLP-compliant workflow traceability
  • “Pulse” mode (1–90 seconds) for gentle resuspension or mixing of viscous or precipitated samples prior to full-speed runs
  • Dual-unit speed selection: switch seamlessly between rpm and RCF (×g) modes with 1-rpm resolution for method transferability across instrument platforms
  • Robust stainless-steel centrifuge chamber and reinforced steel-alloy chassis ensure long-term structural integrity and resistance to chemical exposure and repeated sterilization cycles
  • Four-point mechanical lid locking system with integrated interlock sensor prevents operation unless fully engaged—compliant with IEC 61010-2-020 safety requirements for laboratory centrifuges
  • Active imbalance detection with automatic deceleration and fault logging; overspeed sensor provides independent verification of rotational velocity; motor overheat sensor triggers thermal shutdown before critical threshold is reached

Sample Compatibility & Compliance

The K1015 supports a broad spectrum of tube formats and volumes—from 0.2 mL PCR strips to 50 mL conical tubes—via interchangeable rotors certified to ISO 15197 and ASTM F2119 standards for rotational performance and mechanical safety. All angular rotors (e.g., BRK5424, BRK5436, BRK5448) are balanced to ≤0.5 g mass tolerance and rated for continuous operation at maximum speed. The instrument complies with CE marking directives (2014/30/EU EMC, 2014/35/EU LVD), RoHS 2011/65/EU, and meets essential requirements of ISO 13485 for in vitro diagnostic device support environments. Optional rotor calibration certificates (traceable to UKAS-accredited standards) are available for audit-ready documentation.

Software & Data Management

While the K1015 operates autonomously via its embedded controller, all run logs—including date/time stamp, rotor ID, speed, RCF, duration, and fault events—are retained in internal memory for ≥10,000 cycles. Export is supported via USB 2.0 port (FAT32-formatted drive) for CSV-formatted reports compatible with LIMS integration. Audit trail functionality satisfies FDA 21 CFR Part 11 requirements when paired with validated lab information systems. Firmware updates are delivered through secure, signed packages verified via SHA-256 checksums—ensuring integrity and version control in regulated settings.

Applications

  • Pelleting of bacterial and yeast cells (e.g., E. coli at 12,000 × g for 10 min)
  • Clarification of mammalian cell lysates prior to chromatography or electrophoresis
  • Isolation of plasmid DNA, genomic DNA, and RNA using silica-membrane or phenol-chloroform protocols
  • Preparation of exosomes and extracellular vesicles from conditioned media (≥100,000 × g equivalent achievable via sequential runs with BRK5424)
  • Microcentrifugation of enzymatic reaction mixtures (e.g., kinase assays, restriction digests)
  • High-throughput processing of 96-well plate-compatible PCR strips in molecular diagnostics workflows
  • Routine QC of reagent stability, particle dispersion, and suspension homogeneity in pharmaceutical development

FAQ

What safety certifications does the K1015 hold?

The instrument carries CE marking per IEC 61010-1 and IEC 61010-2-020, complies with EMC Directive 2014/30/EU and Low Voltage Directive 2014/35/EU, and conforms to RoHS 2011/65/EU.
Can the K1015 be used for clinical sample processing under GMP conditions?

Yes—when operated with validated rotors, calibrated speed sensors, and documented maintenance records, the K1015 supports GLP/GMP workflows; optional IQ/OQ documentation packages are available.
Is rotor BRK5424 compatible with 1.5 mL and 2.2 mL microtubes simultaneously?

Yes—the BRK5424 rotor accepts both tube sizes without adapters, maintaining balance and certified RCF across the full speed range.
Does the K1015 require external cooling?

No—it is an ambient-temperature-only centrifuge; heat generation is minimized by the brushless motor and optimized airflow design, keeping internal chamber temperature rise below 8 °C after 30 min at 15,000 rpm.
How is firmware updated?

Via USB flash drive using Centurion’s authenticated firmware updater tool; each release includes digital signature verification and rollback capability.

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