Life Sciences CN

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Fluorescence Lifetime Flow Cytometry (FLFC)

Flow cytometry is a sheath-flow-based technique that uses laser excitation and fluorescence to evaluate the physical and chemical characteristics of cells or other suspended particles in a fluid stream

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Figure 1: Schematic of a fluorescence lifetime flow cytometry setup. A pulsed laser excites a fluorescent sample. Emitted photons (blue, light red, dark red) are filtered by spectrum and collected by single-photon detectors. A time-to-digital converter (Time Tagger) correlates the laser trigger with photon arrival times to measure fluorescence lifetime histograms. These fluorophore-unique histograms enable fluorophore discrimination, even in the case when spectral filters fail due to spectral overlap.

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Dynamic Light Scattering (DLS) Particle Size Analysis

Next-generation multi-angle DLS turnkey design with built-in consistency checks, raw photon access, and intelligent spike filtering for fast, reliable particle sizing.

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Figure 1. The image consists of two main parts: the top half is a schematic of a Dynamic Light Scattering (DLS) setup, and the bottom half shows the DLS analysis and comparison between large and small particles based on the measured data. Top: A laser source emits a monochromatic light that travels horizontally and enters a transparent sample container (a cuvette). Inside this cuvette, several blue particles are shown in random “Brownian” motion. A Single Photon Detector “SPD” is situated at an angle θ from the laser propagation to collect the scattering data from the sample. The correlator acquires and calculates the correlation of the timing data from the detectors in real time. A cable connects the correlator to a computer “PC”, where data analysis is performed. Bottom: Visualization of the different behavior of small and large particles in solution, represented as blue circles (dark and light blue, respectively) and with their hydrodynamic radius (Rs and RL, respectively). Three different analysis plots are shown underneath, from left to right: Left: Intensity vs. Time (s): Two jagged lines represent the fluctuations in light intensity over time.The large particle has slower and smoother fluctuations in light blue color. The small particle shows faster fluctuations in dark blue color. Middle: Autocorrelation Function (ACF) vs. log 𝜏 (s): This plot shows two autocorrelation curves that represent the diffusion behavior of particles suspended in the examined solution. The large particle's curve decays more slowly. The small particle's curve decays faster, reflecting quicker diffusion. Right: Intensity vs. Size (nm): A graph with two sharp Gaussian curves. The left peak is labeled Rs for the small particle. The right peak is labeled RL for the large particle, indicating a size distribution derived from the correlation data.

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Single-Photon Counting Raman Spectroscopy

The single-photon counting Raman spectroscopy combines the principles of Raman spectroscopy with single-photon counting techniques, enabling the detection of weak Raman signals even at low analyte concentrations

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荧光寿命成像 (FLIM)

探索荧光寿命成像（FLIM）这一强大的成像技术，了解其如何以皮秒级精度绘制荧光寿命分布图。Swabian Instruments – 施瓦本仪器® Time Tagger 凭借先进的时间测量电子技术，支持光电倍增管（PMT）、单光子雪崩二极管（SPAD）和超导纳米线单光子探测器（SNSPD）等多种探测器，可实现高分辨率 FLIM 测量，助力前沿科研应用。

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单光子显微镜

您是否希望拥有一台设备，可以捕获单光子显微成像实验设置中的所有信号并通过操作简便的软件分析处理？

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Time-Resolved Photoluminescence (TRPL)

Time-resolved photoluminescence (TRPL) is a powerful technique that measures the photoluminescence decay (emission lifetime) of materials after pulsed excitation, thereby probing their optical and electronic properties. By tracking how excited states relax back to the ground state, TRPL distinguishes between radiative and non-radiative pathways, yielding lifetimes that report on charge-carrier dynamics, trap/defect activity, and other loss mechanisms.

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