Biacore 3000, Cytiva (CAT#: STEM-CTEPO-0070-ZJF)

The Biacore 3000 is manufactured by Cytiva.
The Biacore 3000 processing unit is an established, label-free system for detailed studies of biomolecular interactions. The Biacore 3000 system delivers comprehensive characterization of the interaction, answers questions about the rate constants, affinity, specificity, and determines the active concentration of components. The unique ability to recover and transfer interaction partners directly to MALDI targets for identification and further characterization makes the system highly applicable to fast identification of unknown interactants.
This unit is discontinued by GE, but we offer Service Contracts and can assist with repairs.
Fully re-furbished, calibrated to manufacturer standard.

Condition: Certified pre-owned
Analysis temperature: 4 - 40°C 
Application: Kinetic/affinity characterizationkinetic/affinity screening and profilingconcentration measurement LMW interaction analysisThermodynamic characterization and sample recovery for MS 
Automation: Automated sample loading and injection 
Baseline drift: <0.3 RU/min 
Baseline noise: <0.3 RU (RMS) 
Capacity: Up to 2 x 96 samples 
Depth: 350 mm 
Detection Spots: 4 
Detection technology: Surface plasmon resonance (SPR) biosensor 
Flow rate: < 100 μl/min, through flow cell, steps of 1 μl 
Height: 610 mm 
In-line reference subtraction: Yes (flow cell 2 to 1, 3 to 1, 4 to 1, 4 to 3) 
Includes: Biacore 3000 processing unit, control and evaluation software, handbooks 
Injection volume: 5-750 µl 
Molecular weight detection: >180 Da 
Number of flow cells: 4 (Used individually, in series or as 2 pairs) 
Power consumption: 580 VA 
Sample concentration min.: 10 x 10-12 M 
Sample volume min.: Injected volume + 20 to 80 μl, depending on application 
Voltage: 100-120 V; 220-240 V 
Volume: 0.03 µl 
Weight: 50 kg
Width: 760 mm
Pack size: 1
Warranty: 90-day warranty (US and Canada ONLY)

Recover and characterize interaction partners using MALDI-MS interface.
Elucidate disease mechanisms by characterizing native or recombinant protein interactions.
Define potential drug targets or diagnostic markers.

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