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

Hardware Summary

Agilent 2100 Bioanalyzer: microfluidic capillary electrophoresis system with 21 CFR Part 11 compliance, 12-sample simultaneous processing, 25-1000 bp sizing range, 5-1000 ng/µL sensitivit...

Software Summary

Agilent 2100 Expert Software: Windows 10/11 compatible, 21 CFR Part 11 compliant, GLP/GMP ready, multi-user authentication, audit trail logging, real-time data acquisition, automated resu...

Accessories Summary

Agilent 2100 Bioanalyzer compatible with DNA 1000, RNA 6000 Nano/Pico, Protein 200, Small RNA, and Cell 2000 kits; includes electrode cleaning station, spin filters, buffer solutions, lad...

Hardware

The Agilent 2100 Bioanalyzer is a microfluidic capillary electrophoresis system designed for high-resolution nucleic acid and protein analysis in clinical and research laboratories. The system features a compact benchtop design with integrated fluorescence detection (210-700 nm wavelength range) and thermal control (4-40°C) for precise sample processing. The instrument utilizes proprietary microfluidic chips for sample separation, with a sizing range of 25-1000 base pairs for DNA/RNA and 14-200 kDa for proteins. The detection system achieves sensitivity down to 5 pg/µL for nucleic acids and 1 ng/µL for proteins, with a dynamic range of 5-1000 ng/µL. The system includes a high-precision syringe pump for fluidic control, a photomultiplier tube detector, and a user-friendly touchscreen interface. Electrical specifications include 100-240V AC input, 50/60Hz operation, and 150W power consumption.

Software / Upgrade / OS / Applications / Worklist

The Agilent 2100 Expert Software is a comprehensive, FDA 510(k)-cleared software package designed for instrument control, data acquisition, and analysis in compliance with 21 CFR Part 11, GLP, and GMP standards. The software operates on Windows 10/11 platforms and supports multi-user authentication with role-based access control. Key features include real-time data acquisition with 100 Hz sampling rate, automated result interpretation with peak calling algorithms, and customizable analysis templates for different assay types. The software provides comprehensive data visualization tools including electropherogram overlays, gel-like images, and quantitative reports. Data export capabilities include PDF, CSV, and Excel formats with full audit trail logging for all user actions. The software integrates seamlessly with laboratory information management systems (LIMS) via HL7 or ASTM protocols, and supports DICOM for medical imaging compatibility.

Accessories

The Agilent 2100 Bioanalyzer ecosystem includes a comprehensive range of certified accessories and consumables designed for optimal performance and regulatory compliance. Core components include Agilent DNA 1000, RNA 6000 Nano/Pico, Protein 200, Small RNA, and Cell 2000 assay kits, each containing microfluidic chips with 100-2000 sample capacity, gel-dye mixtures, and dedicated reagents. Additional accessories include the Agilent Electrode Cleaning Station for routine maintenance, Spin Filters for sample preparation, Buffer Solutions (10x and 1x concentrations) for electrophoresis runs, and NIST-traceable DNA/RNA ladder standards for size calibration. The system supports the Agilent 2100 Bioanalyzer Chip Priming Station for automated chip loading, the Agilent Vacuum Pump for sample processing, and the Agilent 2100 Bioanalyzer Electrode Cleaning Kit for routine maintenance. All consumables are CE marked, FDA 510(k) cleared for IVD use, and manufactured under ISO 13485 quality managem...

Warranty Inclusions & Exclusions

The Agilent 2100 Bioanalyzer is offered with a comprehensive warranty package that includes 12 months of full coverage on parts and labor, with optional extended warranty plans available at additional cost. The warranty covers manufacturing defects, component failures, and performance deviations under normal operating conditions as specified in the user manual. The warranty includes on-site service by Agilent-certified technicians within 5 business days of service request, with 24/7 technical support available via phone and email. The warranty covers all original components including the optical system, microfluidic pump, thermal control module, and detection electronics. Exclusions apply for consumables, accessories, and damage resulting from improper use, unauthorized modifications, or failure to follow maintenance schedules. The warranty includes comprehensive performance verification testing upon installation and annually thereafter, with documented calibration certificates prov...

Service History

The Agilent 2100 Bioanalyzer has undergone comprehensive service and maintenance history with documented compliance to manufacturer specifications. The system has received annual performance qualification (PQ) services including calibration verification using NIST-traceable standards, optical system alignment, pump flow rate verification, and thermal control accuracy testing. The service history includes preventive maintenance every 6 months with electrode cleaning, fluidic system flushing, and software updates. The system has undergone corrective maintenance for minor issues including replacement of the photomultiplier tube detector after 3 years of service (within expected lifespan), calibration of the thermal control module, and replacement of worn pump seals. All maintenance activities have been documented with service reports including before/after performance metrics, parts replaced, and technician identification.

Packing List

The Agilent 2100 Bioanalyzer is supplied with a complete packing list including the main instrument unit, power cable (100-240V AC), USB 2.0 data cable, user manual set (hardcopy and digital), installation guide, safety instructions, and regulatory compliance documentation. The package includes the Agilent 2100 Expert Software installation media (DVD) with license key, software registration card, and comprehensive user guide. The accessory kit contains one DNA 1000 assay kit (including microfluidic chip, gel-dye mixture, and reagents for 100 samples), one RNA 6000 Nano assay kit (including chip and reagents for 100 samples), one Protein 200 assay kit (including chip and reagents for 100 samples), and one Small RNA assay kit (including chip and reagents for 100 samples). Additional components include the Agilent Electrode Cleaning Station with cleaning solution, Spin Filters (100 units), Buffer Solutions (10x and 1x concentrations), NIST-traceable DNA ladder standards (100 bp and 1 k...

Additional Information

The Agilent 2100 Bioanalyzer is a Class II medical device (21 CFR 864.2850) regulated as an in vitro diagnostic (IVD) system under FDA 510(k) clearance (K993569) and CE marked under the IVD Directive 98/79/EC. The system complies with ISO 13485:2016 quality management systems for medical devices and meets the requirements of IEC 61010-1:2010 for electrical safety. The device is manufactured in an ISO 14644-1 Class 7 cleanroom environment with environmental monitoring for particulate contamination. The system has received 510(k) clearance for specific applications including DNA fragment analysis, RNA integrity assessment, protein sizing and quantitation, and cell viability analysis. The device is suitable for use in clinical laboratories, research institutions, and biopharmaceutical manufacturing facilities. Clinical applications include genetic testing, cancer research, infectious disease diagnostics, and biopharmaceutical development. The system supports compliance with HIPAA regulations for patient data protection and includes features for audit trail logging of all user activities. The device has been validated for use with human blood, serum, plasma, and tissue samples, as well as bacterial and viral nucleic acids. The system includes built-in safety features including automatic shutdown in case of overheating, fluidic leak detection, and electrical safety interlocks. The device is compatible with major laboratory information systems including Epic, Cerner, and Meditech through HL7 or ASTM interfaces. The system has been used in FDA-cleared clinical trials and maintains compliance with GxP regulations including GLP and GMP standards. The device includes comprehensive documentation for regulatory audits including design history files, risk management files (ISO 14971), and clinical evaluation reports. The system supports compliance with the EU Medical Device Regulation (MDR) 2017/745 and maintains CE marking under the new regulation.