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Oil red o isopropanol solution

Oil-Red O-Isopropanol solution is a staining reagent used in histology and cytology laboratories. It is a solution of the lipophilic dye Oil-Red O dissolved in isopropanol. The solution is used to specifically stain neutral lipids and lipid-rich structures within tissue sections or cell samples.

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5 protocols using oil red o isopropanol solution

1

Renal Lipid Deposition Staining

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Filtered Oil-Red O-Isopropanol solution (Electron Microscopy Science, PA) was diluted with water (6:4). 4 μm kidney sections were incubated with 100 µL freshly prepared Oil-Red O solution for 15 min and counterstained with Hematoxylin Harris Hg Free (VWR, PA) to detect lipid deposition. Glomerular staining was evaluated using a light microscope (Olympus BX 41, Tokyo, Japan) [64] (link).
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2

Detecting Lipid Deposition in Kidney

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Filtered Oil-Red O-Isopropanol solution (Electron Microscopy Science, PA) was diluted with water (6:4). 4μm kidney sections were incubated with 100μl freshly prepared Oil-Red solution for 15 minutes and counterstained with Hematoxylin Harris Hg Free (VWR, PA) to detect lipid deposition. Glomeruli staining was evaluated using a light microscope (Olympus BX 41, Tokyo, Japan)40 (link).
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3

Histological Analysis of Liver Steatosis

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Analyses of serum alanine aminotransferase (ALT) and liver steatosis have been described.(17 (link),18 (link)) For hematoxylin and eosin (H&E) staining, liver tissues were fixed in 10% formalin overnight at 4°C and washed with and stored in 80% ethanol. The fixed tissues were embedded in paraffin, sectioned at 5 μm, and then stained with H&E. For Oil Red O staining, liver tissues were embedded in optimum cutting temperature (OCT) compound, snap frozen, sectioned at 5 μm, and mounted on glass slides, which were fixed in 10% formalin and stained with an Oil Red O iso-propanol solution (Electron Microscopy Sciences, Hatfield, PA).
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4

Histological Analysis of Liver Steatosis

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Analyses of serum alanine aminotransferase (ALT) and liver steatosis have been described.17, 18 For hematoxylin and eosin (H&E) staining, liver tissues were fixed in 10% formalin overnight at 4°C and washed with and stored in 80% ethanol. The fixed tissues were embedded in paraffin, sectioned at 5 μm, and then stained with H&E. For Oil Red O staining, liver tissues were embedded in optimum cutting temperature (OCT) compound, snap frozen, sectioned at 5 μm, and mounted on glass slides, which were fixed in 10% formalin and stained with an Oil Red O isopropanol solution (Electron Microscopy Sciences, Hatfield, PA).
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5

Lipid Quantification in Kidney Cortex

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OCT embedded kidney cortex samples were cryosectioned at 4 μm thickness and stained with Oil-Red O-isopropanol solution (Electron Microscopy Science, PA) diluted 6:4 in water, and then counterstained with Hematoxylin Harris Hg Free (VWR, PA). Sections were then evaluated using a light microscope (Olympus BX 41, Tokyo, Japan).
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