The Vutara 532 microscope and software from Bruker allow for the imaging of structures in cells below the diffraction limit of visible light by sequential imaging and localization of single molecules, and as such is suited for (d)STORM, DNA-PAINT and qPAINT methods. Vutara’s biplane technology provides 3-D imaging during all acquisitions. The large-area Hamamatsu sCMOS camera enables super-resolution data collection on a 40 x 40 µm region. The high-speed detection system and powerful lasers (up to 1000 mW) enable data collection from live and fixed samples with frame rates up to 200 fps. Vutara’s software provides visual and quantitative information from biological samples and can generate stunning 3D images.
Confocal laser scanning microscopy enables optical sectioning of multilayer fluorescent specimens with high contrast by applying a pinhole in the optics. It is therefore possible to image a thin optical slice out of a thick specimen (up to 100 µm) that represents under optimal conditions a slice of approximately 500 nm. Moreover, conventional contrast methods such as the differential interference contrast (DIC) can be used and in reflection mode particles or surfaces can be analyzed.
The CLSM SP8 (1) based on a DMI6000CSB allows precise detection of standard fluorophores in your sample. The system excites via diode laser at 405 nm, Argonlaser combined with AOBS at 458, 488, 514 nm, diode laser at 561 nm and a He/Ne laser at 633 nm. The SP8 (1) has two standard GaAsp photomultipliers (PMTs) and two extremely sensitive Hybrid detectors (HyD), combining PMT and avalanche photodiode (APD) technology. An optional incubation chamber allows imaging of living cells.
The system is almost fully automated and offers with its broad excitation spectra, its automated system parts, the galvo stage and the optional incubation chamber a variety of possible uses.
Immersion objectives are optimized for oil- / glycerol immersion.
Detailed specifications CLSM Leica SP8 (1)
Conventional fluorescence filters for eyepiece vizualization:
HP Z420 Workstation, Windows 7-64 bit, LAS X
Confocal laser scanning microscopy enables optical sectioning of multilayer fluorescent specimens with high contrast by applying a pinhole in the optics. It is therefore possible to image a thin optical slice out of a thick specimen (up to 100 µm) that represents under optimal conditions a slice of app. 500 nm.
The CLSM SP8 (2) based on a DMi8 CEL Compact allows precise detection of fluorophores in your samples. The system excites via diode lasers at 405, 488, 552, or 638 nm. The SP8(2) has two standard GaAsp photomultipliers (PMTs) and one extremely sensitive Hybrid detector (HyD), combining PMT and avalanche photodiode (APD) technology.
The system is optimized for confocal microscopy with standard dyes (DAPI, Alexa488, Alexa555/Cy3, Alexa648/Cy5, etc.) and gives, in combination with its strong and stable diode lasers, convincing results with the given limitations in excitation. The microscope is comparably easy to use as it is pretty stripped down to the components necessary for confocal microscopy in combination with the newest generation of Leica microscopes with a user-friendly touchscreen. All immersion objectives are optimized for oil immersion. „Conventional“ light-microscopy with the Trans-PMT or oculars, respectively, is rather sophisticated as, unlike for the confocal detection, objectives, aperture and filters have to be set manually. The system has no incubation chamber.
Detailed specifications CLSM Leica SP8 (2)
Conventional fluorescence filters for eyepiece visualization:
Total internal reflection fluorescence microscopy (TIRF microscopy) is one example for surface-sensitive microscopy and is therefore only applied to samples that are in contact with a solid, transparent interface (e.g., the mounting glass slide). In TIRF microscopy, the excitation light is (in contrast to conventional fluorescence microscopy) guided to the interface at the angle of total internal reflection. Hence, the excitation light is almost completely reflected, but creates an evanescent (light-)field at the interface, which excites only those parts of the sample that are in close vicinity to the interface (typically the closest 100 to 150 nm). This spatial confinement decreases the noise background (and thus improves the signal-to-noise ratio), but also increases the optical resolution along the optical axis (with respect to usual wide-field or confocal microscopy solutions). Typical applications include imaging of cell structures that are closely located to the cell membrane (e.g., the cytoskeleton) or the transient attachment of biological nanoparticles (such as viruses/virions, vesicles, exosomes) to cell membranes.
The Zeiss Axiovert 200M is an inverted fluorescence microscope equipped with a VisiTron laser-based TIRF extension (excitation at 488 and 561 nm) and a CoolSNAP CCD camera. It provides conventional fluorescence microscopy, FRET and TIRF.