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X cite led illumination system

Manufactured by Excelitas
Sourced in United Kingdom

The X-Cite LED illumination system is a compact and efficient light source designed for use in a variety of laboratory applications. It provides stable and consistent illumination using high-performance LED technology. The system offers adjustable intensity and precise control, making it a versatile tool for various microscopy, imaging, and analysis techniques.

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2 protocols using x cite led illumination system

1

Fluorescent Microparticle Imaging and Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Fluorescently labeled magnetic microparticles were imaged in optical-bottom 96-well plates on an IX83 inverted microscope (Olympus, Tokyo, Japan). Epifluorescence excitation was produced using an X-Cite LED illumination system (Excelitas, Wheeling, IL). An automated stage was employed to obtain 9 acquisitions per well using a pco.panda camera (PCO, Kelheim, Germany) and a 20x air objective (UPlanXApo, NA = 0.80, Olympus). Each acquisition consisted of a brightfield image to locate the microparticles and a fluorescent image (Cy3 filter cube, Edmond Optics, Barrington, NJ) to record the fluorescence intensity. Imaging analysis, including large fluorescent aggregate removal (e.g., dust/hair), calculation of the total microparticle pixel area and total microparticle fluorescence, was performed in Metamorph Advanced software (Molecular Devices, San Jose, CA), as previously described17 (link).
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2

Fluorescent Magnetic Microparticle Imaging

Check if the same lab product or an alternative is used in the 5 most similar protocols
Fluorescently labelled magnetic microparticles were placed in an optical-bottom 96-well plates (Nunc, Thermo Fisher Scientific, Waltham, MA), and placed on a 96-well neodymium magnet array for 3 s to pull microparticles down to the glass surface. An IX83 inverted microscope (Olympus, Tokyo, Japan), equipped with ZeroDrift IX3-ZDC2 continuous focus, was used to measure samples with bright-field illumination from a pE-100 LED (CoolLED, Andover, UK) and epifluorescence excitation light produced by an X-Cite LED illumination system (Excelitas, Wheeling, IL) passing through a Cy3 Olympus dichroic filter cube set (Edmond Optics, Barrington, NJ). Images were acquired through a 20x air objective (UPlanXApo, NA=0·80, Olympus) and recorded on a scientific CMOS PCO.panda camera (PCO, Kelheim, Germany). MetaMorph software (Molecular Devices, San Jose, CA) coordinated imaging measurements, directing a ProScan III xy-stage (Prior Scientific Instruments, Cambridge, UK) to acquire one bright-field image (100 ms, 1·3% LED power) and one (or two) fluorescence image(s) (10 and 100 ms, 25% LED power) at 9 positions within each 96-well. Images were analysed as described previously.20 (link)
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