Photon Counting Detectors

Complete confocal fluorescence microscope that empowers researchers to advance quantitative functional imaging from individual molecules to cells and tissues.

Modular, customizable, time-resolved confocal microscope with single-molecule sensitivity for life and materials science.

Compact FLIM and FCS upgrade kit that adds advanced functional imaging and correlation analysis to existing laser scanning microscopes.

Designed for flexible, sensitive, and precise steady-state and time-resolved spectroscopy across the UV to NIR range and time scales from picoseconds to milliseconds.

Modular lifetime spectrometer designed for flexible fluorescence and photoluminescence measurements in both materials and life science research.

Add spectral and time-resolved photoluminescence to your setup through flexible microscope–spectrometer coupling options.

Get the most out of superconducting nanowire detectors in large-scale quantum communication and computing experiments requiring precise multichannel timing.

Boost your time-resolved experiments with a flexible, high-precision time tagging and TCSPC unit for materials science and quantum sensing.

Scale your photonic quantum computing and detector characterization setups while maintaining performance, flexibility, and high data throughput.

Compact 3-color picosecond laser delivering flexible ns to ms excitation with cost-effective multicolor performance and straightforward operation.

Smart picosecond laser diode heads covering UV-A to NIR, providing the right combination of power, pulse width, and diode type for any time-resolved technique.

VisUV provides clean short pulses and stable timing across key UV and visible wavelengths, including deep UV lines as well as 488 nm and 532 nm.

Enhance your single-photon counting experiments with wide dynamic range and excellent timing precision in the UV and visible even at the highest count rates.

Capture even the weakest signals over large areas with maximum dynamic range and enhanced low-light sensitivity in a compact detector design.

Unlock spatially resolved single-photon detection with a 23-pixel SPAD array, combining low dark counts and precise time tagging for advanced experiments.

Advanced FLIM analysis software for fast, accurate interpretation of lifetime imaging data.

Intuitive, free software solution for real-time, high-precision photon data acquisition, visualization, and initial data analysis.

Advanced software for time-resolved fluorescence acquisition and analysis.

An imaging technique that uses fluorescence lifetimes to generate image contrast.

Investigating how proteins dynamically explore multiple conformational states that control biological function.

Investigating how biomolecules separate into dynamic liquid phases to organize cellular space and regulate biological function.

A time-resolved technique that measures photoluminescence lifetimes to reveal excited-state dynamics in materials.

Studying exciton dynamics, charge carrier processes, and structural properties through optical and time-resolved characterization methods.

Investigating charge-carrier lifetimes and recombination dynamics to enable precise optical characterization of material quality and device performance.

A quantum optical signature revealed by time-resolved photon correlation analysis to identify single-photon emission in materials and nanostructures.

The transmission of information using individual photons, using quantum effects to ensure absolute security.

Quantifying photons per detection event enables direct access to photon-number statistics, providing insight into quantum and statistical properties of light.

An optical technique that analyzes light emission under electrical excitation to reveal electronic properties of electroluminescent materials.

Monitoring environmental signals and trace compounds to understand dynamic changes in natural and engineered environments.

A photon timing technique that measures single-photon arrival times to resolve ultrafast dynamics in fluorescence, materials research, and quantum optics.
Plants are highly dynamic organisms whose structure and function continuously adapt to changing environmental conditions such as light, water availability, and stress. Research in this field explores how plants are structured, how they develop, and how physiological and molecular processes are organized within their tissues and cells. Studying plants therefore focuses on linking tissue organization, cellular behavior, and molecular regulation to plant growth, development, and function.
Plant systems are central to addressing key biological and societal challenges, including food security, environmental sustainability, and climate adaptation. Understanding how plants grow, develop, and respond to environmental cues provides fundamental insight into biological processes and supports the improvement of crops, biomaterials, and bio-based products and technologies. As such, plant research bridges basic research and applied innovation across agriculture, ecology, and biotechnology.
Plants exhibit strong intrinsic autofluorescence arising from molecules such as chlorophyll, flavonoids, and cell wall components. These signals provide valuable structural and functional information but can also complicate conventional intensity-based fluorescence imaging. Resolving biological structures and processes therefore requires advanced fluorescence contrast mechanisms.
Key structural and dynamic processes in plants can be directly observed using fluorescence imaging. These include tissue organization and morphology, cell differentiation and division, and spatial variations in physiological state. At the cellular level, fluorescence signals reveal protein localization, intracellular transport, and dynamic responses to environmental stimuli, linking molecular behavior to plant growth, development, and function.
Quantitative investigation of plant systems relies on fluorescence techniques that provide robust contrast in optically complex samples. Fluorescence lifetime imaging microscopy (FLIM) enables separation of autofluorescence and fluorescent labels and reveals environmental and functional differences beyond fluorescence intensity. Complementary methods such as fluorescence correlation spectroscopy (FCS) and FLIM-FRET quantify molecular mobility, concentration, and interactions, enabling dynamic studies in living plant tissues.
Poster on one pattern analysis for FLIM-FRET, enabling quantitative determination of protein interactions, binding and proximity in living plant cells.
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