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Adapt your existing lab stereo microscopes for fluorescence
The NIGHTSEA Stereo Microscope Fluorescence Adapter adapts just about any stereo microscope (dissecting microscope) for fluorescence with no modification to the microscope itself. The modular design lets you easily switch between several different excitation/emission combinations to work with a variety of fluorescent proteins and other fluorophores. There are now six different excitation/emission combinations available, plus white light.
Up to now we have offered what we call the ‘standard’ base with simple on/off operation, and a separate intensity control option, which we called DIM. As of August 2026 all systems will include the intensity control feature.
The intensity control does not degrade performance compared to the on/off switch. When first energized the unit comes on at the same full power level, while further rotation of the rotary knob reduces the intensity to about 30% of maximum.
Why would you want to reduce the excitation intensity, given that usually you want as much fluorescence response as you can get? There are situations for which it can be beneficial to reduce the excitation, and you can read about them in this article.
This simple system is excellent for

The light head, barrier filter, and filter shield are interchangeable so that you can easily switch between excitation/emission light+filter combinations.
The microscope mounting adapter fits up to 67mm to work with the majority of stereo microscopes. An oversize adapter and an adapter for the Leica EZ4 series are also available.
Once you are set up for one excitation/ emission wavelength combination, additional combinations can be added by purchasing a kit that consists of a light head, barrier filter, and viewing shield. These three elements can be removed and replaced in seconds, and color coding ensures that you are using the right combination. The barrier filter clicks on to the ring adapter magnetically, so it is easy to remove it to switch back to white light viewing.
For more in-depth information on excitations, see this Technical Data Sheet![]()
| Designation | Excitation | Emission | Fluorophores |
| UV – Ultra Violet | 360-380nm | 415nm LP | DAPI, ... |
| VI – Violet | 400-415nm | 450nm LP | CFP, ... |
| RB – Royal Blue | 440-460nm | 500nm LP | GFP, eGFP, fluorescein... |
| RB-GO – Green Only | 440-460nm | 500-560nm BP | GFP, eGFP, fluorescein... |
| CY – Cyan | 490-515nm | 550nm LP | YFP, Venus, Lucifer Yellow... |
| GR – Green | 510-540nm | 600nm LP | DsRed, dTomato... |
The Green-Only (GO) Barrier Filter isolates the green part of the spectrum and is for use with the Royal Blue excitation source. While our other barrier filters are longpass filters this filter is a bandpass, transmitting from approximately 500 to 560nm. The longpass filter has served well for most users who need to visualize green-fluorescent protein (GFP), and if you are exploring fluorescence in nature it is preferable. The primary motivation for adding the green-only filter to the line-up was for the benefit of researchers using GFP in plants such as Arabidopsis thaliana, a common research model. Plants contain chlorophyll, which has a distinctive red fluorescence that can sometimes mask the GFP emission, making it harder to see and photograph.
Microscope Mounting Adapter - standard size fits up to 67mm. Also available for oversize (up to 84mm) and Leica EZ4 Series.
Fluorescence for Education and Outreach
NIGHTSEA Brochure (PDF)
Mazel, C., 2013. Adding Fluorescence to Stereo Microscopes. Microscopy Today, 21(5): 12-17. (PDF)
Aitken, J., V. Ramnath, V. Feygels, A. Mathur, M. Kim, J. Y. Park, and G. Tuell, 2010. Prelude to CZMIL: seafloor imaging and classification results achieved with CHARTS and the rapid environmental assessment (REA) processor. Proc. SPIE 7695, Algorithms and Technologies for Multispectral, Hyperspectral, and Ultraspectral Imagery XVI.
Anastasio, N. C., et al., 2013. Functional status of the serotonin 5-HT2C receptor (5-HT2CR) drives interlocked phenotypes that precipitate relapse-like behaviors in cocaine dependence. Neuropsychopharmacology (13 August 2013). doi:10.1038/npp.2013.199.
Baillie, L. D., V. Hagen, K,. M. Gardner, and S. J. Mulligan, 2011. Functional imaging within individual pain fibres ex vivo with optical microscopy. Journal of Neuroscience Methods, 198(2): 274-279....more citations