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Flash Spectrum ClearFirst-500L Protein Purification System

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Brand Flash Spectrum
Origin Shanghai, China
Manufacturer Type Authorized Distributor
Product Category Domestic
Model ClearFirst-500L
Pricing Available Upon Request
Flow Rate Range 0–40 mL/min
Maximum System Pressure 0.2 MPa (2 bar / 30 psi)
UV Detection Wavelength 280 nm (LED-based)
Wavelength Accuracy ±3 nm
Optical Path Length 2 mm
Conductivity Range 0–500 mS/cm
Fraction Collector Configurations 48-position (18 mm × 150 mm tubes), 130-position (1.5 mL tubes), 88-position (13 mm × 100 mm tubes), 80-position (15 mm × 150 mm tubes), 20-position (50 mL tubes)
Solvent Compatibility Aqueous Buffers Commonly Used in Biomolecular Purification
Detection Systems UV (280 nm), Conductivity, Optional pH (with temperature compensation)
Control Interface Android-based Touchscreen Console + Optional PC Software (ClearFirst PC Edition)
Compliance Designed for GLP-compliant workflows

Overview

The Flash Spectrum ClearFirst-500L Protein Purification System is an integrated, benchtop-scale liquid chromatography platform engineered for reproducible, scalable purification of biomolecules—including recombinant proteins, monoclonal antibodies, nucleic acids, and vaccine antigens—using standard chromatographic modes: affinity, ion exchange, hydrophobic interaction, and size exclusion. Built upon a dual-pump gradient architecture with three-way injection valves and pulse-free peristaltic flow delivery, the system implements classical low-pressure liquid chromatography (LPLC) principles optimized for biological sample integrity. Its pressure rating of 0.2 MPa (2 bar) ensures compatibility with soft- and medium-pressure resins (e.g., Sepharose CL, Capto, and SOURCE series), while maintaining full biocompatibility via inert fluidic pathways constructed from PEEK, PTFE, and chemically resistant elastomers. The system operates under ambient or refrigerated conditions (compatible with standard chromatography cold cabinets), supporting both analytical characterization and milligram-to-gram scale preparative isolation.

Key Features

  • Dual high-precision peristaltic pumps enabling accurate, low-pulsation gradient formation (A/B solvent mixing) without mechanical pulsation artifacts—critical for baseline stability in UV and conductivity detection.
  • Three-way sample injection valve with air-free loading mechanism to prevent bubble entrapment and ensure volumetric accuracy during loop-based or direct-injection sample introduction.
  • 280 nm LED-based UV detector featuring 2 mm pathlength flow cell, ±3 nm wavelength accuracy, and extended operational lifetime (>10,000 hours), optimized for real-time monitoring of aromatic amino acid absorbance in proteins.
  • High-fidelity conductivity detector with identical transducer architecture and calibration methodology to leading international OEMs, delivering linear response across 0–500 mS/cm range for buffer exchange and elution profiling.
  • X-Y matrix-style fraction collector with motor-free base design—enhancing mechanical reliability, reducing electromagnetic interference, and improving safety in cold-room environments.
  • Multi-format tube compatibility: standardized 48-position 18 mm rack (for 15 mL conical tubes), plus optional racks for 1.5 mL, 13 mm, 15 mm, and 50 mL vessels—enabling seamless transition from screening to scaled-up collection.
  • Intelligent peak-triggered fractionation with configurable logic (peak threshold, slope, width, volume, or manual override), minimizing cross-contamination and maximizing recovery yield.
  • Integrated waste diversion three-way valve permitting continuous unattended operation with selective component capture—ideal for multi-step purification protocols requiring intermediate pooling or buffer exchange.
  • Android-powered touchscreen console with intuitive Chinese-English bilingual interface, local method storage, user role management (admin/operator), and embedded instrument self-diagnostic suite.
  • Optional pH sensor module with automatic temperature compensation (ATC), offering resolution and drift performance exceeding typical imported equivalents in physiological pH ranges (pH 3–10).

Sample Compatibility & Compliance

The ClearFirst-500L accommodates a broad spectrum of biomolecular samples—including His-tagged and GST-fusion proteins, IgG subclasses, plasmid DNA, mRNA intermediates, and viral capsid proteins—across diverse buffer systems (Tris-HCl, phosphate, acetate, HEPES) and additive concentrations (NaCl, imidazole, glycerol, arginine). All wetted materials meet USP Class VI and ISO 10993 biocompatibility standards. While not certified for GMP manufacturing, the system supports GLP-aligned data integrity practices through timestamped method logging, electronic signatures (via PC software), and audit-trail-capable user authentication—fully compatible with FDA 21 CFR Part 11 requirements when deployed with validated ClearFirst PC Edition software and controlled IT infrastructure.

Software & Data Management

The ClearFirst workstation—available in embedded Android (v11+) and Windows-compatible PC editions—provides comprehensive method development, execution, and post-run analysis capabilities. Predefined method templates cover common workflows (e.g., Ni-NTA affinity, SP Sepharose cation exchange, Phenyl HP hydrophobic interaction). All methods are stored in encrypted local databases with version control, supporting rapid recall and parameter adjustment. Chromatograms (UV, conductivity, pH if installed) are saved in vendor-neutral CSV and native binary formats, with optional export to third-party analysis tools (e.g., OriginLab, GraphPad Prism). PC Edition adds remote monitoring, scheduled runs, automated report generation (PDF/Excel), and integration with LIMS via configurable API endpoints.

Applications

The ClearFirst-500L serves core applications in academic research laboratories, CROs, and early-stage biomanufacturing facilities: purification of CRISPR-Cas9 complexes prior to functional assays; isolation of extracellular vesicles from conditioned media using size-exclusion chromatography; buffer exchange and desalting of antibody fragments post-cleavage; parallel optimization of elution gradients for bispecific IgG purification; and preparative isolation of histone variants for epigenetic studies. Its modular architecture allows straightforward adaptation to novel ligands (e.g., custom affinity matrices) and emerging modalities such as circular RNA or virus-like particles—without hardware modification.

FAQ

What chromatographic techniques does the ClearFirst-500L support?
Affinity, ion exchange, hydrophobic interaction, and size exclusion chromatography—all using standard prepacked or custom-packed columns rated for ≤2 bar operating pressure.
Is the system compatible with cold-room installation?
Yes—the compact footprint (W×D×H: 560 × 470 × 420 mm) and motor-free fraction collector enable stable operation inside standard 4 °C chromatography refrigerators.
Can I import/export methods between instruments?
Yes—method files are portable across ClearFirst-500L units via USB drive or network share when using PC Edition software.
Does the system support regulatory compliance documentation?
The PC Edition software includes 21 CFR Part 11-ready features (electronic signatures, audit trails, secure user roles); validation documentation packages are available upon request for qualified customers.
What maintenance is required for long-term reliability?
Routine replacement of pump tubing (every 3–6 months depending on usage), annual calibration of UV and conductivity detectors, and periodic verification of valve timing and fraction positioning accuracy using reference standards.

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