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Analysis software version 3

Manufactured by Olympus
Sourced in Germany

AnalySIS software, version 3.2, is a data analysis and imaging solution developed by Olympus. It allows for the processing and analysis of digital microscopy images and data. The software provides basic image editing and measurement tools.

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4 protocols using analysis software version 3

1

Fluorescence Microscopy Image Acquisition

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Preparations were observed in a Zeiss Axioplan 2 microscope equipped with appropriate fluorescence filter sets. Black-and-white images were taken either with a cooled F-View CCD camera (DAPI- and CGH-stained preparations) or an Olympus CCD monochrome camera XM10, and captured separately for each fluorescent dye with either AnalySIS software, version 3.2 (Soft Imaging System GmbH) or with cellSens 1.9 digital imaging software (Olympus Europa Holding), respectively. The images were pseudo-coloured and merged using Adobe Photoshop CS4 and CS5 (Adobe Systems Inc.).
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2

Fluorescence Microscopy Protocols for Dragonfly Cytogenetics

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Rhionaeschna species preparations were observed in a Zeiss Axioplan 2 fluorescence microscope (Carl Zeiss, Jena, Germany). Black-and-white images were recorded with a cooled F-View CCD camera and captured with AnalySIS software, version 3.2 (Soft Imaging System GmbH, Münster, Germany). Preparations of A. cyanea were observed in a Leica DMLB fluorescence microscope equipped with a Leica DFC350 FX monochrome digital camera and Leica IM50 software, version 4.0 (Leica Microsystems Imaging Solutions Ltd., Cambridge, UK). Images of chromosomes were captured separately for each fluorescent dye and then pseudocolored (light blue for DAPI and red for Cy3) and superimposed using Adobe Photoshop, version 7.0 or Adobe Photoshop CS5.
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3

Fluorescent Microscopy Imaging Protocol

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Preparations from FISH experiments were observed under a Zeiss Axioplan 2 microscope (Carl Zeiss Jena, Germany). Black-and-white images were recorded with a cooled F-View CCD camera using AnalySIS software, version 3.2 (Soft Imaging System GmbH, Münster, Germany). In all preparations, images were captured separately for each fluorescent dye, pseudocoloured (light blue for DAPI, green for fluorescein and red for Cy3) and superimposed with Adobe Photoshop, version 7.0.
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4

Visualizing Au-NPs Encapsulation in Transporter Vesicles

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In this study, Au-NPs were employed as a representative drug model for encapsulation within TFs. The distinctive high contrast of Au-NPs against the background was utilised to clearly demonstrate their successful encapsulation within TFs. The morphologies of TF and TF-encapsulated Au-NPs were examined following negative staining using 2% uranyl acetate for 10 min. Transmission electron microscopy (TEM) (Philips CM12 TEM (FEI U. K. Ltd., Altrincham, UK) was used to investigate the morphology of the vesicles at 80 kV and images were captured with a Megaview III camera and AnalySIS software, version 3.2 (Soft Imaging System GmbH, Münster, Germany). TEM was performed at Central Biotechnology Services, Cardiff University.
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