Specifications for cell^M

Multi-fluorescence 3-D time-lapse
    imaging
Reduced photo-bleaching
Graphical experiment set-up
Data archiving, processing and analysis
Back to main page Print
Key FeaturesSpecificationsApplications

Hardware Olympus microscopes BX50 -BX61, BX61WI, IX50-IX81
CCD, EMCCD cameras, various models
Imaging Computer (latest generation PC)
Illumination system MT10
Short arc burners, 150 W Xenon or Mercury-Xenon
8 Filter positions diameter 25 mm
Filter switch min. 85 ms (neighbouring positions)
Attenuation 7 levels, 4% - 100%
Attenuation switch  <85 ms
Shutter, on/off time 5 ms
Operation sequentially
Hardware control Control board with additional CPU, independent from imaging PC System coordinator
Temporal resolution 10 ms (camera 1 ms)
Timing precision ca. 15 ms
Camera control trigger (level trigger if accepted by camera)
Peripheral device control via TTL pulses optional: 3 BNC connectors
Multi-task acquisition with hardware switch (z-position, exciter filter etc.), 50 ms exposure 3-4 full frames/sec with sequential hardware switch
Experiment set-up and control Graphical interface Experiment Manager
Drag-and-drop alignment of command icons
7-D acquisition (xyz, excitation and emission colour, time, stage position)
Loop-in-loop capability (repetition of complex command groups)
Experiments with varying acquisition speed and camera exposure
Autofocus, repeatedly during experiment
Live image display and online analysis
User interaction: pause, resume, set marker
Imaging software cell^M
Structured database for multi-dimensional data handling and storage
Image types: (n x 16) bit, 8 - 24 bit export and import
Image processing: filters, extended focal imaging, shading and background correction, arithmetic…
Measurements and analyses: number, length, distance, area, circumference, angle, grey value, histograms, line profiles, tables, statistics, diagrams…
Fluorescence analyses: intensity kinetics, ratioing, Δ F/F
Spectral unmixing for optimised colour resolution
Deblurring, SliceViewer, VoxelViewer
Macros and automated functions: imaging C module, macro recorder
Options Piezo-electric objective drive (all microscopes) or nosepiece drive (IX51, IX71, IX81 only)
TIRFM lasers and illumination combiners, multi-line
FRET, hardware and analysis (different algorithms)
Deconvolution for resolution enhancement
3-D rendering for three-dimensional image generation
Particle detection and tracking
Upgradeability To cell^R




cell^M
  Brochures
Manuals
System Charts
Glossary
Contact Us
Compare Products