Claudia Jaffe

Co-Founder & Executive Vice President of Business Development, Lumencor

Claudia Jaffe, Ph.D., is Co-Founder & Executive Vice President of Business Development at Lumencor (Beaverton, OR).

Coupling of a solid-state light engine to an inverted fluorescence microscope. Locations 1–5 marked in yellow correspond to the points in the light path used for throughput measurements reported in the table. The green line shows the direction of the light path from the collimating adapter input to the sample plane.
Lasers & Sources

Optimizing solid-state illumination, from source to sample plane

Dec. 10, 2020
When photons from a light engine are getting lost on their way to the microscope’s sample plane, follow this path to find the failure point(s).
Data courtesy of Mark Sanders, Director, Twin Cities University Imaging Centers, University of Minnesota
To investigate the bleaching rate of fluorescein isothiocyanate (FITC) with different light sources, 1mM FITC in water under a coverslip was collected with a Nikon E800 and 40x, 0.75 numerical aperture objective at 1 s intervals for 1 min using a CoolSNAP MYO camera (Photometrics). The red dotted line represents a 120 W metal-halide source at full power with the microscope shutter set to block illumination between exposures using an enhanced green fluorescent protein (eGFP) filter set. The green solid line is similar, using the cyan line of the self-shuttering Lumencor SpectraX Light Engine at full power, pulsing at 1 ms intervals during the 1 s exposure. Note t0 = 2,000 counts and 5,081 counts for metal-halide and light engine, respectively.

FLUORESCENCE MICROSCOPY/LIGHT SOURCES: Light engines: Lighting the way to mercury-free microscopy

Nov. 19, 2013
Fluorescence microscopes and other scientific instruments still rely on mercury-based light sources -- despite associated costs and hazards and many mandates to eliminate the ...