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Bx53 bright field microscope

Manufactured by Olympus
Sourced in Japan

The BX53 is a bright field microscope designed for routine laboratory applications. It features high-quality optics and sturdy construction to provide reliable performance. The microscope is capable of providing clear, high-contrast images for a variety of sample types.

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5 protocols using bx53 bright field microscope

1

Microscopic Imaging of IHC Samples

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All DAB IHC-stained slides were viewed and photographed using the Olympus BX53 bright field microscope with an Olympus DP21 digital camera (Olympus, Tokyo, Japan). The Olympus FV1200 confocal microscope (Tokyo, Japan) was used for the IF IHC-stained slides with subsequent 2D deconvolution using CellSens Dimension 1.11 software (Olympus).
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2

Quantitative Immunohistochemistry and Protein Expression Analysis

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All the experiments were conducted at least in triplicates unless mentioned otherwise. IHC staining intensity was observed and analyzed by an expert pathologist in a single-blinded fashion using a BX53 bright field microscope (Olympus Corporation, Japan). Quantification of protein expression for IHC and WB was performed using ImageJ software 1.8.0 (https://imagej.nih.gov/ij/). The images were RGB stacked, and the color threshold was adjusted according to the expression of specific proteins in the tissue section. For quantification, the expression was presented as a composite score of the percent area of the total tissues using ImageJ software. The statistical/imaging parameters used for the various transcriptomic analyses have been detailed with their explanations in their respective sections in the manuscript. GraphPad Prism 7.0 software (GraphPad Software, Inc., USA) was used for the data analysis of IHC and RT-qPCR quantified datasets.
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3

Organoleptic and Microscopic Analysis of Medicinal Plants

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Organoleptic characters such as color, odor, and taste were recorded from the dried raw materials of taxonomically authenticated plants. Macroscopic characters such as nature, texture, and external features were also noted. Hand sections were carried out to record the microscopic features, followed by histochemical studies performed with various stains such as safranin, toluidine blue, and Lugol’s iodine solutions. The microscopic features were recorded, and the images were captured using Olympus BX53 bright field microscope.
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4

Bright Field Microscope Imaging of Dispersions

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Microscope imaging of the dispersion was carried out using a BX53 bright field microscope (Olympus, Tokyo, Japan) equipped with a 100× oil-immersion objective lens. Approximately 5 μL of the dispersion was loaded in a microchamber consisting of two glass coverslips separated by a Parafilm ® spacer and sealed with silicone grease. During the observation, the sample temperature was held at 25°C using a KM-1 Microwarm Plate (KITAZATO Co., Shizuoka, Japan). Static images were captured by a DP74 microscope digital camera (Olympus, Tokyo, Japan), and analyzed using ImageJ software (U.S. NIH).
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5

Muscle Fillets Staining Protocol

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Muscle fillets were dissected in 1% BSA in PBS, fixed in 4% formaldehyde in PBS for 20 min, and washed twice in 1% BSA in PBS. Periodic acid stain (PAS) was used as previously described (Yamada et al, 2018 (link)). The samples were mounted in glycerol and imaged on an Olympus BX53 Brightfield microscope using a ×4 objective lens.
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