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Bx50f microscope

Manufactured by Olympus
Sourced in Japan

The BX50F is a compact and versatile upright microscope designed for a wide range of laboratory applications. It features a binocular observation tube, a built-in Köhler illumination system, and a trinocular observation port for photomicrography or digital imaging. The BX50F provides reliable and consistent performance for routine microscopy tasks.

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5 protocols using bx50f microscope

1

Visualizing Bacterial Colony Spreading

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Time-lapse videos were used to observe the colony margins, as previously reported (Sato et al., 2021b (link)). The plate was inverted on the sample stage and observed from underneath using an All-in-One Fluorescence Microscope BZ-X800 (KEYENCE). Images were visualized with a phase contrast objective LUCPlanFLN 20× (Olympus). The phase contrast microscope images were taken every 30 s. The images were analyzed, adjusted, and cropped using a BZ-X800 analyzer software (KEYENCE).
Time-lapse videos were made around the colony spreading of GFP-expressing F. johnsoniae strains using a BX50F microscope (Olympus). The culture plate was placed on a sample stage, and a cover glass was carefully placed over the colony. After the top surface of the dendrites formed was imaged using phase contrast microscopy, fluorescence signals in the same area were observed to track the cells using confocal laser scanning fluorescent microscopy (CLSM) with an objective lens of UPlanFl 100× (Olympus) and ANDOR iXon EMCCD camera (Oxford Instruments, Abingdon, UK) in combination with Andor iQ3 software (Oxford Instruments). Exposure time of each image was typically 100 ms (excitation light: 490–510 nm, emission light: 520–550 nm). Fluorescence images were taken every 3 s for 10 min, and movies were produced.
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2

Evaluating Root Hair Deformation in C. glauca Seedlings

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C. glauca seedlings were placed in hydroponic culture. Salt stress was applied gradually and plants were inoculated separately with either Frankia strain CcI3 or Frankia strain CeD, as described above. Two days after inoculation, root hair deformation was evaluated through micrographs of small lateral roots acquired with a Micro Publisher 3.3 RTV digital camera (QImaging) and a BX50F microscope (Olympus). For each treatment, five plants were used and three lateral roots were analyzed per plant. A total of 180 lateral roots and 12,217 root hairs were observed. Root hair deformation intensity was evaluated as described in Clavijo et al. (2015 (link)). For each micrograph, root hairs were observed and the following scoring was used: 0, no deformation; 1, straight root hair with tip swelling; 2, only one change in growth direction; 3, more than one change in growth direction but no bifurcation; 4, one or more bifurcations. At least two independent experiments were performed.
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3

Histological Evaluation of Decalcified Specimens

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Following micro‐CT, the specimens were decalcified using 10% formic acid for 1 week. After decalcification, the specimens were paraffin embedded in a Leica APS 300S auto processor. Histological sections (10 μm in thickness) were prepared from the mid‐point of the defects in the coronal plane using a Leica Microtome RM 2145. Two sections per sample were placed on Leica ApexTM Superior adhesive slides and stained with haematoxylin and eosin (H&E). Digital images of the stained sections were obtained using the Olympus BX50F microscope with an Olympus DP72 digital colour camera (Olympus, Japan). All the H&E‐stained sections were evaluated by a blinded musculoskeletal pathologist.
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4

Immunohistochemical Analysis of CC Tumors

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Clinical CC tumors and paracancerous tissues were collected and fixed in 4% paraformaldehyde solution. After dehydration with a gradient of 50%, 70%, 80%, 90%, and 95% anhydrous ethanol, the tissues were immersed in a 1:1 mixture of anhydrous ethanol and xylene for half an hour and then made transparent in a pure xylene solution. Following paraffin embedding, CC tumor and adjacent non-cancerous tissues were subsequently sectioned into 4-μm slices. Following rehydration, the sections were subjected to microwave treatment in a citrate buffer to facilitate antigen recovery. Endogenous peroxidase activity was inhibited by 3% H 2 O 2 . Subsequently, the sections were incubated with a 5% BSA solution for 30 min, followed by incubation with the primary anti-ATF4 (dilution 1:800; Affinity Biosciences, Jiangsu, China; DF6008), anti-p-GCN (dilution 1:800; Affinity Biosciences; AF8154), AND anti-ASNS (dilution 1:800; Affinity Biosciences; DF7398) at 4 °C overnight and then with the corresponding secondary antibody. Treatment with DAB (3,3′-diaminobenzidine) was applied to the sections, and hematoxylin served as the counterstain. Finally, the staining was observed using an Olympus BX50F microscope (Olympus, Tokyo, Japan).
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5

Microscopic Analysis of Microorganisms

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All the samples were observed before any later analysis was done under an OLYMPUS BX50F microscope equipped with a digital camera. Samples (500 mg) were suspended in deionized water and several stain methods were followed: methylene blue to evidence sheaths or mucilage; lugol (IIK) to differentiate starch/pyrenoids; Gram to observe bacterial walls. Three slides were prepared per sample and the microorganisms present in three random traverses from each slide were quantified on a semiquantitative scale from 1 to 3: 1= 1–20 %, 2= 21–50%, 3>50%.
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