beam-splitting optics w-view gemini (Hamamatsu)
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Beam Splitting Optics W View Gemini, supplied by Hamamatsu, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/optical+beam+splitting+system/w+view+gemini+image+splitting+optics/pm37471225-158-18-22
Average 90 stars, based on 1 article reviews
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Transgenic Assay:Article Title: Calcium-mediated rapid movements defend against herbivorous insects in Mimosa pudica Article Snippet: .. The transgenic M. pudica was imaged in real time with a motorized fluorescence stereomicroscope (SMZ25, Nikon) equipped with a 1× objective lens (NA = 0.156, P2-SHR PLAN Apo, Nikon) and a sCMOS camera (ORCA-Flash4.0 V2, Hamamatsu Photonics) or a motorized macro zoom microscope (Axio Zoom.V16, Zeiss) equipped with a 1× objective lens (NA = 0.25, PlanNeoFluar Z, Zeiss), an Fluorescence:Article Title: Calcium-mediated rapid movements defend against herbivorous insects in Mimosa pudica Article Snippet: .. The transgenic M. pudica was imaged in real time with a motorized fluorescence stereomicroscope (SMZ25, Nikon) equipped with a 1× objective lens (NA = 0.156, P2-SHR PLAN Apo, Nikon) and a sCMOS camera (ORCA-Flash4.0 V2, Hamamatsu Photonics) or a motorized macro zoom microscope (Axio Zoom.V16, Zeiss) equipped with a 1× objective lens (NA = 0.25, PlanNeoFluar Z, Zeiss), an Microscopy:Article Title: Calcium-mediated rapid movements defend against herbivorous insects in Mimosa pudica Article Snippet: .. The transgenic M. pudica was imaged in real time with a motorized fluorescence stereomicroscope (SMZ25, Nikon) equipped with a 1× objective lens (NA = 0.156, P2-SHR PLAN Apo, Nikon) and a sCMOS camera (ORCA-Flash4.0 V2, Hamamatsu Photonics) or a motorized macro zoom microscope (Axio Zoom.V16, Zeiss) equipped with a 1× objective lens (NA = 0.25, PlanNeoFluar Z, Zeiss), an |
![Optical measurement setup for simultaneous surface height measurement and SRG patterning. ( a ) Schematic of the optical components used to project the interference pattern for SRG writing through the digital holographic microscope. The light input (488 nm) to the microscope is through a <t>polarization</t> maintaining fibre, output of which is collimated by lenses L2. After adjusting the polarization states with quarter- and half-wave plates (QWP and HWP, respectively), the two beams are combined with a 50:50 beam splitter BS2. The combined beam is then focused onto the back focal plane of the microscope objective by lens L1, resulting in two collimated beams exiting the objective. The angles of these two beams are controlled by the XY mounts for the ends of the optical fibre. ( b ) DHM and AFM images of an SRG with \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$4\ \upmu \hbox {m}$$\end{document} 4 μ m period inscribed with the optical setup shown in ( a ) using left- and right-handed circular polarizations for the inscription. The grating cross sections are compared in ( c ), with the DHM measurement shown in orange color and the AFM measurement in blue.](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_5031/pmc07665031/pmc07665031__41598_2020_76573_Fig1_HTML.jpg)