Delivers flexible testing, powerful software and a user-friendly interface, features that help both clinical and basic researchers optimize their overall workflow. The system has the capacity to conduct 5-color analysis using either a single (488nm) laser or a dual (488nm/635nm) air-cooled laser configuration. Coupled with the ability to perform tube or plate based automated analysis, the system enables you to easily manage and automate every aspect of your flow cytometric analysis. The FC 500 incorporates ADC technology, the most advanced method of color compensation available. Combined with high resolution acquisition electronics, its proven algorithm provides superior correction of spectral overlap for more accurate results. With ADC technology, biological samples can be used for automated color compensation, without the limitations of latex beads. 20-bit Digital Signal Processing (DSP) on the system is responsible for excellent linearity, drift-free amplification and accurate color compensation. High resolution color compensation is available during acquisition and in Listmode analysis, increasing the flexibility of the system. Both optical and digital systems work together to yield unrivalled visualization of low intensity fluorescence populations.

Specifications

Platform FC500
Resolution 0.5 μm diameter particles. HPCV is <2% to <4% depending on the laser.
Performance <600 MESF for APC, <600 MESF for FITC, <300 MESF for PE
Optics/Laser Power 488 nm argon ion laser (20 mW), 635 nm solid state laser (25 mW)
Flow Cell BioSense 150 μm x 450 rectangular channel with an integral lens
Signal Processing Digital System with 4 decade data display
Software CXP software
Power Requirements 100-240 VAC, 50/60 Hz, Requires dedicated lines
Temperature Range 16°C - 32°C
Humidity Restrictions 35%-85% (non-condensing)
Regulatory Status IVD
Installation Category II (per IEC 1010-1 standard)
Weight 84.8 kg / 187 lb
Width 97.8 cm / 38.5 in
Depth 88.9 cm / 35 in
Height 61 cm / 24 in
UNSPSC 41116015

NOT ALL PRODUCTS ARE AVAILABLE IN ALL COUNTRIES
PRODUCT AVAILABILITY AND REGULATORY STATUS DEPENDS ON COUNTRY REGISTRATION PER APPLICABLE REGULATIONS

The listed regulatory status for products correspond to one of the below:
IVD: In Vitro Diagnostic Products. These products are labeled "For In Vitro Diagnostic Use."
ASR: Analyte Specific Reagents. These reagents are labeled "Analyte Specific Reagents. Analytical and performance characteristics are not established."
CE: Products intended for in vitro diagnostic use and conforming to European Directive (98/79/EC). (Note: Devices may be CE marked to other directives than (98/79/EC)
RUO: Research Use Only. These products are labeled "For Research Use Only. Not for use in diagnostic procedures."
LUO: Laboratory Use Only. These products are labeled "For Laboratory Use Only."
No Regulatory Status: Non-Medical Device or non-regulated articles. Not for use in diagnostic or therapeutic procedures.