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Vs 120 slide scanner

Manufactured by Hamamatsu Photonics
Sourced in Germany

The VS 120 Slide Scanner is a high-resolution digital slide scanning system designed for a variety of applications. The device captures detailed images of microscope slides, enabling efficient digitization of biological samples for further analysis and archiving.

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5 protocols using vs 120 slide scanner

1

Automated Immunofluorescent Imaging Protocol

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Automated imaging of immunofluorescent sections stained as described above (“Immunohistochemical and immunofluorescent assay”) with Ki67 (labeled with Alexa Fluor 488 secondary), Cldu (labeled with Alexa Fluor 568), and DAPI staining. Images were acquired on an Olympus VS 120 Slide Scanner with a Hamamatsu ORCA-Flash 4.0 camera and a 40× 0.65 NA objective. Filter cubes were standard Olympus DAPI, FITC (for Alexa Fluor 488), and TRITC (for Alexa Fluor 568) cubes. Exposure times and illumination intensities were kept constant across time points and replicates.
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2

Cresyl Violet Staining and Brightfield Imaging

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Sections were stained in 0.1% Cresyl violet solution (Cresyl violet, Sigma Cat# C5042) for 10 min, rinsed quickly in distilled water, dehydrated in 95% ethanol, and left in xylene before being cover-slipped with Permount (Thermo Fischer Scientific, SP15-500). Brightfield images were taken in the Olympus VS-120 slide-scanner with Hamamatsu digital camera C11440 and processed using the Olympus VS-Olyvia 2.9 software.
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3

Fluorescence Imaging of Cellular Structures

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Fluorescence imaging was performed on an Olympus VS120 slide scanner, equipped with an X-Cite 120 LED light source and a Hamamatsu Flash 4.0 sCMOS camera or a spinning-disk confocal microscope (UltraVIEW; PerkinElmer), comprising an inverted stand (Axiovert 200 M; Carl Zeiss Microimaging, Jena, Germany) and a spinning-disk confocal head (CSU-X1; Yokogawa Corporation of America) with Velocity acquisition software (PerkinElmer) and dual cameras: a Hamamatsu C9100-23B EMCCD camera and a Hamamatsu Orca-R2 camera. Fluorescence channels were acquired sequentially. DAPI fluorescence was acquired with a 405 nm diode laser and a 445 (W60), 615 (W70) dual bandpass emission filter. Red (Alexa 546) fluorescence a 561 nm diode laser and a 445 (W60), 615 (W70) dual bandpass emission filter.
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4

Automated Immunofluorescent Imaging Protocol

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Automated imaging of immunofluorescent sections stained as described above (“Immunohistochemical and immunofluorescent assay”) with Ki67 (labeled with Alexa Fluor 488 secondary), Cldu (labeled with Alexa Fluor 568), and DAPI staining. Images were acquired on an Olympus VS 120 Slide Scanner with a Hamamatsu ORCA-Flash 4.0 camera and a 40× 0.65 NA objective. Filter cubes were standard Olympus DAPI, FITC (for Alexa Fluor 488), and TRITC (for Alexa Fluor 568) cubes. Exposure times and illumination intensities were kept constant across time points and replicates.
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5

Pancreatic Insulin Immunostaining Post-RYGB FMT

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Pancreatic tissues from pre- and post-RYGB FMT mice were fixed for 24 hours in 4% paraformaldehyde in PBS (pH 7.4). Paraffin sections (7 μm thick) were obtained separately from pancreas and stained for insulin (Dako Canada) (catalog IR00261-2). insulin-immunostained sections were scanned using an Olympus VS120 slide scanner and analyzed with NDP.view2 plus software from HAMAMATSU. insulin immunostaining was calculated by an automated positive pixel count algorithm to determine total β-cell area, islet number per total pancreatic area, and islet size.87 (link)
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