[:ru]Времяразрешенный флуоресцентный микроскоп PicoQuant MicroTime 200[:en]Microtime 200[:]

• Полностью конфокальная система, объединенная с лазерным блоком, инвертированным микроскопом и мультиканальным модулем детекции
• Готовые к работе диодные лазеры для возбуждения на разных длинах волн от 375 до 900 нм
• До 4х полностью параллельных каналов детекции с использованием оптимизированных через ПО ФЭУ, твердотельных (SPAD) и гибридных (Hybrid PMT) детекторов
• Времяразрешенный подсчет единичных фотонов (Time-Correlated-Single Photon Counting, TCSPC) и режим TTTR для изучения быстрой динамики в режимах FCS и FLIM
• Пьезо-сканирование для 2D и 3D-съемки времен жизни и точного позиционирования
• Два дополнительных выходных порта для дополнительных модулей, например, спектрографов
• Продвинутое и простое в управлении ПО для получения данных, анализа и визуализации SymPhoTime 64
• Уникальные опции апгрейда до двухфокусного FCS, одновременного АСМ/FLIM, измерений в области УФ
• Опция STED для флуоресцентной микроскопии сверхвысокого разрешения
• Новый гальвосканер FLIMbee, сочетающий высокую скорость (возможности rapidFLIM) и точность позиционирования.

 

Flexible excitation subsystem
The excitation subsystem of the MicroTime 200 consists of a pulsed diode laser driver of the PDL Series and different laser heads with pulses in the picosecond time regime (additional CW mode is available as an option). The available wavelengths range from 375 to 900 nm.The laser power and repetition rate can be flexibly adjusted by the laser drivers of the PDL Series. The multichannel laser driver PDL 828 "Sepia II" even allow to address several lasers in parallel enabling advanced techniques like Pulsed Interleaved Excitation (PIE).The laser heads are integrated in one Laser Combining Unit (LCU) for easier handling, attenuation and coupling into an optical fiber. An alternative incoupling port at the MicroTime 200 can accommodate additional excitation sources such as Ti:Sapphire lasers for multi-photon excitation schemes. Using our dedicated Two-Photon-Excitation unit, the output from external lasers can be easily coupled to the main optical unit of the MicroTime 200.

 

Choice of scanning technologies
The MicroTime 200 can be equipped with different devices for scanning an image: A galvo scanner for quick image acquisition or piezo devices for maximum flexibility in terms of usable wavelengths. The great versatility of the MicroTime 200 platform is complemented by the FLIMbee galvo scanner which can provide scanning speeds ranging from very slow to fast while maintaining high precision. This high degree of flexibility in speed allows for applications ranging from Phosphorescence Lifetime Imaging (PLIM) to fast fluorescence lifetime measurements using rapidFLIM. Furthermore, with its high precision and sensitivity, the FLIMbee scanner is optimally suited for super-resolution microscopy via STED, enabling imaging down to the single molecule level.
A MicroTime 200 equipped with a FLIMbee scanner is a good choice for Single Molecule Detection (SMD) methods such as spFRET, PIE-FRET, (STED-)FCS, FLCS, FLCCS, dual-focus FCS (2fFCS), and even anisotropy measurements. Additionally, Two-Photon Excitation (TPE) with descanned and non-descanned detection is possible.
The core of the FLIMbee galvo scanner consists of three high precision oscillating mirrors with excellent linearity, repeatability and low drift. The two y-axis galvo mirrors ensure that the laser beam is stationary at the entrance of the objective. This mirror configuration minimizes vignetting of the image field and ensures a constant focal volume over a wide scan range. The FLIMbee scanner provides a minimal pixel size of 10 nm when using a 100x objective.

 

Detection subsystem with single photon sensitivity
The MicroTime 200 was specially designed for single molecule studies and thus offers unique optics with vastly reduced light absorption. In this confocal microscope, scanning is facilitated through a piezo table optionally combined with a high precision PiFoc element for 3D imaging. The choice of piezo scanning ensures a high repositioning accuracy and stability, which is essential for single molecule studies.The MicroTime 200 can be configured for up to six individual detection channels. Each channel can be equipped with a different detector, chosen from a variety of sensitive detectors. The detectors offer ideal solutions depending on the wavelength to be detected, the signal brightness and the excited state lifetime of the investigated emitters. The choice of detectors include PMA Hybrid detectors, optimized SPADs for efficiency or timing as well as dedicated detectors for experiments in the deep UV.
Timing with picosecond resolution
Time-resolved microscopy requires the registration of not only the photons themselves, but also their position in time and, for imaging, in space. The ideal technique for that purpose is the Time-Tagged Time-Resolved (TTTR) data acquisition developed by PicoQuant, which is an variation of the classical method of Time-Correlated Single Photon Counting (TCSPC). The advantage of TTTR data acquisition mode is that it allows to perform vastly different measurement procedures, like FLIM, FCS or even coincidence correlation ("antibunching"), based on just one fundamental data format. The TTTR format ist supported by all available TCSPC electronics from PicoQuant. Using these high-end integrated devices fluorescence lifetimes down to a few picoseconds or even up to ms for phosphorescence and luminescence studies can be easily resolved.
Intuitive data handling and analysis
Based on the sophisticated data collection and handling, the system software SymPhoTime 64 supports a multitude of methods, such as intensity time trace, burst analysis, lifetime histogramming, Fluorescence Correlation Spectroscopy (FCS), Fluorescence Lifetime Correlation Spectroscopy (FLCS), Fluorescence Lifetime Imaging (FLIM), Förster Resonance Energy Transfer (FRET) and anisotropy, to name only a few.SymPhoTime 64 data handling maintains a transparent data structure where all derived data is maintained in one workspace, including a log file to keep track of all measurement and analysis steps.A large number of algorithms for those methods are already integrated in SymPhoTime 64, providing a analysis platform for ready-to-publish data. At the same time, SymPhoTime 64 offers enhanced flexibility for the integration of novel, cutting edge algorithms by the user. A dedicated scripting language interface allows to modify and expand the analysis routines. In addition to data analysis within SymPhoTime 64, data can be exported to standard formats for external analysis.Our interactive user forum as well as our regularly held SymPhoTime training days offer outstanding support for new and advanced users.
Scientific guidance and user training
PicoQuant annually holds the European short course on "Time-resolved Microscopy and Correlation Spectroscopy". The course is intended for individuals wishing an in-depth introduction to the principles of time-resolved fluorescence microscopy and its applications to the Life Sciences. This 3-day event consists of lectures as well as instrumentation and software hands-on training. For details see the course website.
PicoQuant also hosts a forum that serves as a knowledge exchange platform for users of the company's systems, components and software packages.