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775 nm sted system

Manufactured by Abberior
Sourced in Germany

The 775 nm STED system is a specialized laboratory equipment designed for super-resolution microscopy. It utilizes Stimulated Emission Depletion (STED) technology to achieve resolution beyond the diffraction limit of light. The system operates at a wavelength of 775 nm and is a core component for advanced imaging applications in various scientific disciplines.

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2 protocols using 775 nm sted system

1

Multi-modal 3D Imaging Techniques

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Multi-channel 3D image series were acquired with a Perkin Elmer Ultra VIEW VoX 3D spinning disk confocal microscope (SDCM) using a 100x oil immersion objective (NA 1.4) (Perkin Elmer), with a z-spacing of 200 nm. Images were recorded in the 405, 488, 561 and 640 nm channels. Images of RNA FISH samples were acquired with a Leica SP8 DLS laser scanning confocal using a 63x oil immersion objective (NA 1.4) (Leica, Wetzlar, Germany), with a z-spacing of 300 nm. Stimulated emission depletion (STED) imaging was performed with a λ = 775 nm STED system (Abberior Instruments GmbH, Göttingen, Germany), using a 100x Olympus UPlanSApo (NA 1.4) oil immersion objective. Images were acquired using the 590 and 640 nm excitation laser lines. Nominal STED laser power was set to 80% of the maximal power of 1250 mW with 20-30µs pixel dwell time and 20 nm pixel size. For 3D STED data 60% of the STED laser power was used for fluorescence depletion in the Z-axis and RESCue illumination scheme was used to minimize bleaching. Sampling frequency was 30 nm in all three axis (xyz). All STED images shown (except 3D STED images) were linearly deconvolved with a Lorentzian function (fwhm 50 nm) using the software Imspector (Abberior Instruments GmbH).
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2

STED Microscopy of SNAP-Labeled Cells

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3.33 × 103 SNAP.OR3 expressing cells were seeded on 15-well µ-Slides Angiogenesis (ibidi) and infected as described above. Prior to fixation, cells were incubated with 2 µM SNAP-Cell 647-SiR (New England Biolabs) for 30 min at 37°C, washed three times and fixed with 4% PFA (15 min). STED microscopy was performed using a 775 nm STED system (Abberior Instruments GmbH, Germany) equipped with a 100 x oil immersion objective (NA 1.4; Olympus UPlanSApo). STED Images were acquired using the 590 and 640 nm excitation laser lines while the 405 and 488 laser lines were acquired in confocal mode. Nominal STED laser power was set to 80% of the maximal power (1250 mW) with 20 µs pixel dwell time and 15 nm pixel size. STED Images were linearly deconvolved with a Lorentzian function (FWHM 50 nm) using the Richardson-Lucy algorithm and the software Imspector (Abberior Instruments GmbH).
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