Pre-owned / Used 1999 AGILENT TECHNOLOGIES 2100 Bioanalyzer ELECTROPHORESIS SYSTEMS for Sale

Hardware Summary

Agilent 2100 Bioanalyzer with microfluidic capillary electrophoresis, 12-sample simultaneous analysis, 488nm/635nm dual laser excitation, ±2% sizing accuracy, 10-15bp resolution range, US...

Software Summary

Agilent 2100 Expert Software vB.02.08 or later, Windows 10/11 compatible, FDA 21 CFR Part 11 compliant, GLP/GMP compliant data logging, automated assay setup, real-time data visualization...

Accessories Summary

Agilent RNA 6000 Pico Kit, DNA 1000 Kit, Protein 230 Kit, Agilent 2100 Electrode Cleaner, Agilent 2100 Buffer Kit, Agilent 2100 Chip Priming Station, Agilent 2100 Vacuum Pump, USB 2.

Hardware

The Agilent 2100 Bioanalyzer is a microfluidic capillary electrophoresis system designed for precise nucleic acid, protein, and cell analysis. The system features a compact benchtop design with integrated laser-induced fluorescence detection, thermal control module, and microfluidic chip interface. Key specifications include: detection sensitivity of 0.5 pg/µL for dsDNA, dynamic range of 5 orders of magnitude, sample volume requirement of 1 µL per assay, run time of 30-40 minutes per chip, power consumption of 100-240V AC at 50/60Hz, dimensions of 32.5 cm (W) x 26.5 cm (D) x 27.5 cm (H), weight of 12 kg. The system incorporates a high-precision syringe pump for fluidic control, a Peltier-based thermal module for temperature stability, and a photomultiplier tube detector with 488nm and 635nm excitation wavelengths. The device is equipped with a touch-sensitive LCD display for local operation and status monitoring.

Software / Upgrade / OS / Applications / Worklist

The Agilent 2100 Expert Software provides comprehensive control, data acquisition, and analysis capabilities for the Bioanalyzer system. The software operates on Windows 10/11 platforms and is compliant with FDA 21 CFR Part 11, ensuring electronic record integrity and audit trail functionality. Key features include automated assay setup with predefined protocols for RNA, DNA, and protein analysis, real-time data visualization with customizable plot views, automated peak detection and sizing with ±2% accuracy, multi-user access control with role-based permissions, electronic signature capability for regulatory compliance, and comprehensive data export options including PDF, CSV, and direct LIMS integration. The software supports GLP/GMP compliant data logging with timestamped records, automated calibration verification, and system suitability testing. Data integrity features include checksum validation, write-protection mechanisms, and secure data archiving.

Accessories

The Agilent 2100 Bioanalyzer ecosystem includes a comprehensive range of certified accessories and consumables designed for optimal performance and regulatory compliance. Core consumables include Agilent RNA 6000 Pico Kit (50 assays, 50-5000 nt range), DNA 1000 Kit (100 assays, 25-1000 bp range), and Protein 230 Kit (100 assays, 14-230 kDa range). Essential accessories include the Agilent 2100 Electrode Cleaner for maintaining electrode integrity, Agilent 2100 Buffer Kit for consistent electrophoresis conditions, Agilent 2100 Chip Priming Station for microfluidic chip preparation, and Agilent 2100 Vacuum Pump for fluidic control. Additional components include certified USB 2.0 cables for data transfer, universal power adapters with international certifications, calibration standards for fluorescence intensity verification, and Agilent 2100 Quality Control Kits for system performance validation.

Warranty Inclusions & Exclusions

This pre-owned Agilent 2100 Bioanalyzer is offered with comprehensive warranty and support options designed to meet clinical laboratory requirements. The seller provides a 12-month limited warranty covering all mechanical and electrical components, including the laser excitation system, thermal control module, and detection optics. The warranty includes on-site service response within 5 business days for critical failures affecting clinical operations, with parts replacement guaranteed within 10 business days. Extended warranty options are available at additional cost, including 24-month and 36-month coverage with enhanced service level agreements. The warranty covers all manufacturer defects and includes calibration verification services to maintain CE-IVD compliance. Technical support is provided by Agilent-certified engineers with expertise in capillary electrophoresis systems, including remote troubleshooting capabilities and on-site intervention when required.

Service History

This Agilent 2100 Bioanalyzer has undergone comprehensive preventive maintenance and performance verification according to manufacturer specifications. The service history includes quarterly calibration verifications using certified reference materials, annual performance qualification testing with system suitability standards, and bi-annual preventive maintenance procedures. Maintenance records document laser alignment verification, photomultiplier tube sensitivity calibration, thermal control module recalibration, and fluidic system integrity checks. The system has been serviced by Agilent-certified engineers with documented compliance to ISO 13485 quality management standards. All maintenance activities are recorded in the system's electronic service log with timestamps, technician identification, and verification signatures. The service history includes replacement of consumable components such as electrode cartridges, microfluidic chip interfaces, and optical filters according ...

Packing List

The complete packing list for this Agilent 2100 Bioanalyzer includes all original components, accessories, documentation, and certification materials required for installation and operation. The system is packaged in a custom-designed shipping crate with foam padding and electrostatic discharge protection. Included components are: main Bioanalyzer unit with integrated thermal control module, 120V/240V universal power adapter with international plug adapters, 2-meter certified USB 2.0 data cable, Agilent 2100 Expert Software installation media (DVD) with license key, comprehensive user manual in English and additional language options, quick reference guide, safety instructions, and regulatory compliance documentation. The accessory kit includes Agilent RNA 6000 Pico Kit (50 assays), DNA 1000 Kit (100 assays), Protein 230 Kit (100 assays), Agilent 2100 Electrode Cleaner, Agilent 2100 Buffer Kit, Agilent 2100 Chip Priming Station, Agilent 2100 Vacuum Pump, and certified calibration st...

Additional Information

This Agilent 2100 Bioanalyzer represents a premium-grade capillary electrophoresis system designed for high-precision molecular analysis in clinical and research laboratories. The system is CE-IVD marked for in vitro diagnostic use and complies with European Medical Device Regulation (MDR) 2017/745, ensuring conformity with essential safety and performance requirements for medical devices. The Bioanalyzer is also compliant with FDA Quality System Regulation (21 CFR Part 820) and meets the requirements for Clinical Laboratory Improvement Amendments (CLIA) in the United States. The system has been validated for use in clinical applications including nucleic acid quality control, protein characterization, and cell analysis, with demonstrated performance in accordance with ISO 15189 standards for medical laboratories. Clinical applications include next-generation sequencing sample preparation, CRISPR validation, gene expression analysis, and protein biomarker research. The system integrates seamlessly with laboratory information management systems (LIMS) through standardized data export formats, enabling automated result reporting and compliance with electronic health record (EHR) systems. The Bioanalyzer's microfluidic technology reduces sample and reagent consumption by up to 90% compared to traditional gel electrophoresis methods, while maintaining superior resolution and reproducibility. The system's compact design and benchtop configuration make it suitable for installation in standard clinical laboratories with limited bench space. All components are manufactured under ISO 13485 quality management systems, and the system undergoes rigorous testing for electromagnetic compatibility (EMC) in accordance with IEC 61326-1 standards. The device is classified as Class IIa medical device under the European MDR framework and requires annual performance verification for continued compliance.