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Coolpix b500

Manufactured by Nikon
Sourced in Japan

The Nikon Coolpix B500 is a compact digital camera with a 16.0-megapixel sensor and a 40x optical zoom lens. It has a 3-inch LCD screen and supports 1080p video recording.

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8 protocols using coolpix b500

1

Exebacase Treatment of Bacterial Growth

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Overnight cultures of MW2 and CFS-1155 were diluted 1:100 in TSB and grown at 37°C with aeration. At OD600 1.0 (~5 × 108 CFU/mL), 0.8 mL was transferred into Fisherbrand Disposable Cuvettes (1.5 mL semi-micro cell, polystyrene, catalog no. 14–955-127). For treated cultures, exebacase was added to final concentration of 64 µg/mL. For untreated cultures, PBS alone was added. Cultures were immediately visualized using an MP4 video format on a Nikon Coolpix B500 camera set at 1080 resolution, 30 FPS, 29 min (maximal time allowed). The resulting video was cropped, and playback speed was adjusted to cover the first 15 min in a 14-s video with resolution set to 720 p.
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2

Excisional Skin Wound Healing in Mice

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A single full-thickness excisional skin wound was made on the shaved flank skin of mice using a 4 mm-diameter biopsy punch (Kai Industries, Japan). Wounds were imaged using a Nikon COOLPIX B500 digital camera each day and wound size measured using calipers19 on a daily basis for up to nine days post injury. Wound area was calculated as described19 and presented as the percentage of initial wound size.10 (link) In a second set of experiments, anti-podoplanin antibody (clone 8.1.1, 100 μg)13 (link),17 (link),20 (link) or IgG isotype control were intravenously injected 24 hours (h) before and again 24 h after wounding. Wound size was monitored for three days post injury.
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3

Exebacase Treatment of Bacterial Growth

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Overnight cultures of MW2 and CFS-1155 were diluted 1:100 in TSB and grown at 37°C with aeration. At OD600 1.0 (~5 × 108 CFU/mL), 0.8 mL was transferred into Fisherbrand Disposable Cuvettes (1.5 mL semi-micro cell, polystyrene, catalog no. 14–955-127). For treated cultures, exebacase was added to final concentration of 64 µg/mL. For untreated cultures, PBS alone was added. Cultures were immediately visualized using an MP4 video format on a Nikon Coolpix B500 camera set at 1080 resolution, 30 FPS, 29 min (maximal time allowed). The resulting video was cropped, and playback speed was adjusted to cover the first 15 min in a 14-s video with resolution set to 720 p.
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4

Edible Film Color and Opacity Analysis

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The color characteristics (lightness (L*), redness (a*), and yellowness (b*)) values of the tested films were evaluated using a Hunter Lab colorimeter [MiniScan EZ, HunterLab, Reston, VA, USA].
Film opacity [25 (link)] was determined using the following equation based on the film absorbance at 600 nm and the film thickness: Opacity=AX
In this equation, A represents the film absorbance at 600 nm, and x represents the film thickness (mm). The film opacity was expressed as A600/mm.
For the film appearance, using a handheld digital camera [Coolpix B500, Nikon, Tokyo, Japan], a digital image of the tested edible films was taken.
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5

Imaging and Quantifying Plant Seedling Morphology

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Images of seedlings exhibiting phloroglucinol staining were taken on a Leica MZ16 stereo microscope equipped with a Leica DFC320 digital camera. Images of hypocotyl and root length were taken on a Leica SAPO stereo microscope equipped with a Nikon Coolpix B500 camera. Aniline blue-stained cotyledons and root cell bulging were imaged with an Olympus FV1000 setup using an inverted IX81 stand and FluoView software (FV10-ASW version 01.04.00.09) (Olympus Europa GmbH, Hamburg, Germany) equipped with a 10x objective (NA 0.3). For assessing cell bulging a projection of a 5 μm z-stack encompassing seven individual optical sections was used. Aniline blue fluorescence was excited at 405 nm using a diode laser and detected at 425 to 525 nm. H2DCFDA and EGFP fluorescence excitation was done at 488 nm using a multi-line argon laser and detected at 502 to 536 nm. For the direct comparisons of fluorescence intensities, laser, pinhole and gain settings of the confocal microscope were kept identical when capturing the images from the seedlings of different treatments. Scan speeds were set at 400 Hz and line averages at between 2 and 4. Measurements on digital micrographs were done using ImageJ software [84 (link)]. Images were adjusted for color and contrast using Adobe Photoshop 2020 software (Adobe, San Jose, USA).
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6

Timed Up and Go Test for Mobility Assessment

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The TUG test is a simple yet commonly used test for evaluating lower limb muscle function, mobility and fall risk [54 (link)]. Participants completed an 8-foot TUG by moving from a seated position to standing, walking 8 feet, turning and returning to a seated position as quickly as possible. Time to complete the task was recorded using a video camera (Nikon, Coolpix B500) and analysed using Quintic Biomechanics version 26.0 (Quintic Consultancy Ltd., Birmingham, UK). Participants completed the task three times, with each attempt separated by 30 s of rest. Participants were instructed to complete the course as fast as possible and the fastest time was recorded and used in later analysis.
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7

Observing halophilic cell growth

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WCL brine samples were kept in the laboratory at room temperature and exposed to natural light. Cells were observed to slowly grow under these conditions. Subsamples of these brines were inoculated in a classical culture medium for halophiles (Rodriguez-Valera et al., 1980) slightly modi ed to match the pH and Mg concentrations of the WCLs (Tables S2-S3). Growth was monitored by optical microscopy using a Zeiss Axioplan microscope equipped with a Nikon Coolpix B500 color camera for image acquisition.
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8

Visualizing GFP Expression in Agroinjected Plants

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GFP fluorescence was verified with a FastGene ® blue/green LED flashlight (FG-11; NIPPON Genetics, Tokyo, Japan), which was used to irradiate (excitation: 489 nm; emission: 520 nm) leaves and fruit at the mature red ripening stage (about three days after agroinjection) at a distance of ~ 10 cm from each organ in the dark. To photograph the irradiated leaves, a yellow UV filter (NIPPON Genetics) was mounted to the camera (Nikon Coolpix B500, Tokyo, Japan) lens to filter out blue light, and to allow GFP fluorescence to be visualized. Fluorescence was also verified in controls at the same time. The location of GFP fluorescence was visually assessed and confirmed. Three controls were used for both methods at the same time as the agroinjection into ripe fruits and leaves using infiltration solution: (a) without any A. tumefaciens; (b) A. tumefaciens without any plasmid; (c) A. tumefaciens with a constitutive promoter (CaMV-35S) + sGFP in the plasmid.
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