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Posted in | Spectrofluorometers

X-Cite 120LED High – Power Broad Spectrum LED Solution from Lumen Dynamics

The new X-Cite® 120LED offers a totally new perspective to LED illumination with no compromise. The 120 LED offers a completely new perspective to LED illumination without any compromise. The 120LED offers exceptional field uniformity and superior optical power at the specimen level with the broadest spectrum of fluorescence illumination through manual, PC and TTL control.

With 25,000h guaranteed LEDs and no need to replace modules or lamps, X-Cite 120LED offers convenience and simplicity to researchers permitting them to focus on their experiments instead of equipment maintenance.

Key Features

The key features of the X-Cite 120LED from Lumen Dynamics are:

  • Maximum power and individual LED control

  • Adaptable plug-and-play modularity

  • Unmatched field uniformity at the specimen

  • Rapid wavelength switching to capture fast cell dynamics

  • Flexible triggering for simultaneous or sequential imaging

  • Live-cell mode to limit cellular and photobleaching damage

  • Use up to four high power LED modules with fine excitation control while balancing illumination intensity between channels and protecting specimens against photodamage.

  • X-Cite® microscope adaptors lead the industry in field uniformity without the need for alignment, while saving time on maintenance and ensuring peace-of-mind in experimental results.

  • Each LED module and associated optical components can be quickly swapped in the field for another wavelength depending on the needs of your application.

  • Each LED module is designed to integrate and easily interchange individual excitation filters, allowing accelerated wavelength switching beyond the scope of motorized filter wheels.

  • Triggering sequences can be combined with a high degree of control over individual LED intensity to excite and image multiple fluorophores when examining very fast moving specimens or for live-cell ratio imaging.

  • Researchers can extend the time frame of their live-cell imaging experiments by reducing the degree of free radical formation caused by the continuous illumination of fluorescent proteins.

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