Fluorescence Imaging

Fluorescence imaging

What is fluorescence imaging?

Fluorescence imaging is an imaging technique that visualizes cells and molecules by fluorescently labeling them using fluorescent dyes and fluorescent proteins. Generally, cells and molecules are colorless and transparent, so they cannot be observed as they are. There are various staining methods other than fluorescent labeling to visualize cells; however, many of them can damage the cells. Fluorescent dyes and fluorescent proteins used in fluorescence imaging can label cells while they are alive, enabling live cell imaging of organisms. This allows us to obtain various information such as cell structure and function, and molecular interactions. Fluorescence imaging has become an important tool in the development of biology.

Confocal microscopy

Fluorescence imaging made significant advancements thanks to the Nobel Prize in Chemistry awarded in 2008 to three researchers: Professor Osamu Shimomura, Professor Martin Chalfie, and Professor Roger Y. Tsien. The prize recognized their discovery and development of the green fluorescent protein (GFP). GFP is a protein isolated from the bioluminescent jellyfish. Professor Shimomura was the first to successfully isolate GFP from jellyfish after observing that it emits green light when exposed to ultraviolet radiation. Subsequently, Professor Martin Chalfie contributed to understanding the fluorescence emission mechanism and successfully expressed GFP within living cells using genetic engineering techniques. Additionally, Professor Roger Y. Tsien elucidated the molecular mechanism of GFP chromophore formation, allowing the creation of artificial fluorescent proteins that emit various colors beyond green. This breakthrough enabled the expression of different colored fluorescent proteins within living organisms, facilitating simultaneous tracking of multiple biological phenomena, including the analysis of interactions between different proteins.

Structure of green fluorescent protein

Figure 1: Structure of green fluorescent protein (GFP)

Example of fluorescently stained cell imaging

Figure 2: Example of fluorescence-stained cells

What is fluorescence microscopy?

A fluorescence microscope is a type of microscope used for imaging cellular structures through fluorescence. A sample labeled with a fluorescent dye or protein is irradiated with excitation light, and the fluorescence emitted from the sample is focused by an objective lens and photographed by a camera.

 

A fluorescence microscope mainly consists of an optical system including a light source, filter, dichroic mirror, and objective lens. Figure 3 shows a schematic diagram of a commonly used epifluorescence microscope. In an epifluorescence microscope fluorescence microscope, light emitted from the light source (excitation light) has its unwanted wavelengths cut off by an excitation filter. The excitation light is then reflected by a dichroic mirror and irradiated onto the sample through an objective lens. The sample irradiated by the excitation light emits fluorescence, which is passed through the objective lens, dichroic mirror, and fluorescence filter (absorption filter) before being guided to a detector such as an eyepiece lens or camera.

 

In recent years, various fluorescence imaging techniques have been developed, including confocal microscopy, super-resolution microscopy, light-sheet microscopy, and multiphoton microscopy. These fluorescence imaging techniques enable observation at higher resolution, faster speeds, and greater depths than ever before.

Figure 3: Schematic diagram of an epifluorescence microscope

See how imaging advances with today's leading microscopy techniques

Confocal microscopy

Confocal microscopy enhances image resolution by blocking out-of-focus light, enabling high-contrast, 3D imaging of cells with precise optical sectioning.

Super-resolution microscopy

An imaging technique that is used to observe with resolution beyond the diffraction limit of conventional optical microscopes.

Light-sheet microscopy

Explore light-sheet microscopy with Hamamatsu’s high-sensitivity CMOS cameras, MEMS mirrors, and LCOS-SLM modulators—ideal for fast, low-phototoxic 3D imaging.

Multiphoton microscopy

Multiphoton microscopy enables deep, low-phototoxic imaging using ultrashort lasers. Explore Hamamatsu’s PMTs, MPPCs, SLMs, and MEMS mirrors for high precision.

Fluorescence lifetime imaging microscopy

FLIM maps fluorescence lifetimes for high-contrast imaging, independent of intensity. Explore Hamamatsu’s HPDs ideal for sensitive, time-resolved data.

Explore experimental methods and solutions

Calcium imaging

Calcium imaging tracks intracellular Ca²⁺ activity using fluorescent probes. Explore Hamamatsu’s ORCA cameras, PMTs, and W-VIEW GEMINI for fast, precise imaging.

Förster resonance energy transfer

FRET enables real-time analysis of protein interactions via energy transfer between fluorophores. Hamamatsu’s ORCA cameras and optics deliver precise dual-wavelength imaging.

Photostimulation

Photostimulation enables precise light-based control of cells. Hamamatsu cameras, SLMs, PMTs, and MPPCs support FRAP, optogenetics, and high-speed neural imaging

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