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Vs120 fl

Manufactured by Olympus
Sourced in United States

The VS120-FL is a digital slide scanning microscope designed for fluorescence imaging applications. It features a high-resolution camera and advanced optics to capture detailed images of fluorescently-labeled samples.

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3 protocols using vs120 fl

1

Fluorescence Imaging System Specifications

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The basic specifications of fluorescence imaging systems has been reported previously.24 Briefly, macroscopic images were captured using a fluorescence reflectance imaging system (OV100; Olympus, Tokyo, Japan) equipped with a 150 W xenon light source and a color digital CCD camera (DP71; Olympus). Excitation and emission filters for ICG fluorescence imaging were 730 ± 22.5‐nm band‐pass and 770‐nm long‐pass filter, respectively. High‐power view was observed using a multi‐wavelength laser scanning microscope (IV100; Olympus) equipped with a 748‐nm diode laser with 17 mW power output and a photomultiplier tube. The emission filter to detect ICG fluorescence was a 779‐nm long‐pass filter. Tissue sections were scanned using a fluorescence virtual microscopy system (VS120‐FL; Olympus) equipped with a 200 W mercury light source (X‐Cite exacte; Excelitas Technologies, Waltham, MA, USA) and a monochrome digital CCD camera (ORCA‐R2; Hamamatsu Photonics, Hamamatsu, Japan). Excitation and emission filters for ICG fluorescence were 708 ± 37.5‐nm band‐pass and 809 ± 40.5‐nm band‐pass filter, respectively. Fluorescence images are shown in grayscale or pseudo‐colors.
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2

Fluorescence Imaging for Live Cells and Tissues

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Live cell images were captured using a fluorescence inverted microscope (IX‐73; Olympus Corporation) or a fluorescence virtual slide scanning system (VS120‐FL; Olympus Corporation). VS120‐FL was also used for tissue section imaging. Macroscopic images of mice were captured using an in‐house NIR fluorescence imaging system consisting of excitation light by LEDs at a peak of 660 nm (SMBB660‐1100‐02; Ushio Opto Semiconductors) and a monochrome camera (GS3‐U3‐15S5M‐C, Point Grey Research) equipped with a 692‐nm long‐pass filter (FF01‐692/LP‐25‐D; Semrock). All fluorescence images were converted to pseudo‐colors by cellSens Dimension software (Olympus Corporation) or Image J software (National Institutes of Health). The analysis of fluorescence images was performed by Image J software.
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3

Multimodal Imaging for Cell and Tissue Analysis

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Microscopic imaging was performed using a fluorescence reflectance imaging system (OV100; Olympus Corporation, Tokyo, Japan) and a multi-wavelength laser scanning microscope (IV100; Olympus) to acquire wide-field and high-power images, respectively [18 (link)]. Live cells and tissue sections were scanned using a fluorescence virtual microscopy system (VS120-FL; Olympus) [18 (link)]. Endoscopic imaging was performed using an in-house endoscopic system, as described previously [14 (link)]. ICG fluorescence was excited by a xenon light source through a 600 ± 200-nm band-pass filter and detected by a sensitive electron-multiplying charge-coupled device camera (MC285SPD-L0B0; Texas Instruments, Dallas, TX, USA) through a 842.5 ± 17.5-nm band-pass filter. As a flexible endoscope, a bronchoscope fiberscope (BF-XP60; Olympus Medical Corporation, Tokyo, Japan), 2.8 mm in diameter with a single biopsy channel, was used. Fluorescence images were shown in grayscale or pseudo-colors.
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