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Cell imaging software for life science microscopy

Manufactured by Olympus
Sourced in Germany

Olympus Cell Imaging Software is a versatile software solution designed for life science microscopy. It provides a comprehensive set of tools for image acquisition, analysis, and processing, enabling researchers to capture and evaluate high-quality microscopic images.

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5 protocols using cell imaging software for life science microscopy

1

Liposome-Based Delivery of Cathepsin Inhibitor

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Example 7

Liposomes were prepared as: aliquots of lipids (2.6 mM of egg phosphatidylcholine (Avanti Polar Lipids, Inc.) and 0.1 mM of lipidated inhibitor) supplied as chloroform solutions are placed into vials to form thin films by removing chloroform by evaporation under vacuum. Dry films are then hydrated by adding of 0.1 mg Alexa Fluor 555™ (Invitrogen) containing 0.01 M phosphate buffer, pH 7.4. Active endocytosis of macrophages was stopped by incubation at 4° C. during 15 minutes. Next, 200 μl of liposomes were placed on the cells and incubated for 15 minutes at 4° C. After incubation cells were washed by PBS and examined with an Olympus fluorescent microscope (Olympus IX 81, Olympus) with Imaging Software for Life Science Microscopy Cell. Non-functionalized liposomes (Lip-Alx) and liposomes functionalized with NS-629 (NS-Lip-Alx) were examined with an Olympus fluorescence microscope (Olympus IX 81, Olympus) with Imaging Software for Life Science Microscopy Cell. FIG. 6 shows representation of liposomes with lipidated Cathepsin inhibitor targeting efficiency in primary mouse immune cells.

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2

Histological Assessment of Preserved Heart Tissue

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The second portion of isolated heart were trimmed into small pieces and preserved in 10% formalin for 24 h. Specimens were cut in section of 3–5 μm in thickness and stained by hematoxyline-eosin stain. The specimen was mounted by disterene phthalate xylene (D.P.X). The photomicrographs of each tissue section were observed using Cell imaging software for Life Science microscopy (Olympus soft imaging solution GmbH, Munster, Germany-magnification: 40×). The grading system used for assessment of parameters was [–: absence of change; +: 0–30% area shows changes; + +: 30–60% area shows changes; + + +: 60–100 area shows changes].
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3

Tissue Histology Processing and Imaging

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The isolated tissue was trimmed into small pieces and preserved in 10% formalin for 24 h. Specimens were cut in sections of 3–5 μm in thickness by microtome and stained by hematoxylin-eosin. The specimens were mounted by disterene phthalate xylene (DPX). The photomicrographs of each tissue section were observed using Cell Imaging software for Life Science microscopy (Olympus Soft Imaging Solution GmbH, Munster, Germany).
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4

Formalin-Fixed Tissue Histology

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The isolated tissue was trimmed into small pieces and preserved in 10% formalin for 24
hr. Specimens were cut in sections of 3–5 µm in thickness by microtome and stained by
hematoxylin-eosin. The samples were mounted by disterene phthalate xylene. The
photomicrographs of each tissue section were observed using Cell Imaging software for Life
Science microscopy (Olympus Soft Imaging Solution GmbH, Munster, Germany).
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5

Hepatocyte Proliferation and Morphometry

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Paraffin-embedded liver specimens were cut in 4 μm sections and stained with hematoxylin and eosin (H-E). To assess the rate of hepatocyte proliferation, the number of hepatocytes undergoing mitosis was counted in 10 high-power fields (HPF) in 72 hs after HP (mitotic index) [29 (link)].
To determine the number and the size of parenchymal cells per slide, the hepatocytes nuclei were counted and internuclear distance was measured in 5 HPF using Cell Imaging Software for Life Science Microscopy (Olympus) at 72 h after HP.
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