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Analysis software package

Manufactured by Olympus

Olympus Analysis Software Package is a comprehensive data analysis and visualization tool designed for use with Olympus laboratory equipment. The software provides a suite of tools for processing, analyzing, and visualizing data from various experimental and analytical techniques. It offers a user-friendly interface and a range of features to support data management, statistical analysis, and presentation.

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2 protocols using analysis software package

1

Nanoparticle Characterization by SEM and TEM

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Scanning electron microscopy was carried out using a Zeiss SUPRA 40VP system. Samples were prepared by spreading 2 μL of the nanoparticle suspension in water on a silicon substrate. The sample was dried under ambient conditions and then sputter-coated with a gold-platinum alloy (15 s, 20 mA). Micrographs were acquired using the InLens mode with an accelerating voltage of 10 kV. Particle sizes were measured on micrographs acquired at a magnification of 200 000× using the Olympus Analysis software package. To ensure size measurement accuracy, at least 250 measurements were made per sample. For transmission electron microscopy measurements, a 4 μL aliquot of sample was adsorbed onto a holey carbon-coated grid (Lacey, Tedpella), blotted with Whatman 1 filter paper and plunge-frozen into liquid ethane at −180 °C using a vitrobot (FEI). Frozen grids were transferred onto a Talos electron microscope (FEI) using a Gatan 626 cryo-holder. Electron micrographs were recorded at an accelerating voltage of 200 kV using a low-dose system (50 e Å−2) and keeping the sample at −175 °C. Defocus values were −3 μm. Micrographs were recorded on a 4 × 4 K Ceta CMOS camera.
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2

Immobilized Transaminase Enzyme Characterization

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The carrier SNPs were produced as previously described. [3] All chemicals, solvents, enzymatic assay kit and enzymes were purchased from Sigma (Switzerland). A detailed procedure for the production of immobilized and protected enzyme has been published by us for a β-galactosidase. [4] We have adapted this procedure to the selected transaminase. Scanning electron microscopy experiments were carried out using a Zeiss SUPRA ® 40VP scanning electron microscope. A 2 µL drop of the sample was spread on freshly cleaved mica substrates, dried, and sputtercoated with a gold-platinum alloy. Electron micrographs were acquired with an accelerating voltage of 20 kV using the InLens mode. Particle size analyses were carried out using the Olympus ® AnalySIS software package.
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