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62 protocols using digital camera

1

Wound Macroscopic Assessment and Measurement

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During the experimental period, the macroscopic appearance of the wound and surrounding skin was recorded at the time of the dressing change using a digital camera (Sony Corp., Tokyo, Japan). Erythema on the periwound skin and necrotic tissue on the wound bed were observed. The wound areas were measured using the ImageJ software (National Institutes of Health, Bethesda, MD) and the wound areas relative to that on PWD 1 were calculated.
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2

Behavioral Monitoring in Multi-Chamber Apparatus

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A multi-chamber acrylic glass apparatus (4.5 × 6.5 × 5.5 inches per chamber) with a removable cover with breathing holes was used for this study. Behavior was recorded by a Sony digital camera pointed at a mirror positioned 2 inches directly underneath the apparatus.
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3

Rat Nerve Transposition and Stimulation

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The rats were fixed on a laboratory-made operating table after anesthesia. The affected limb was held firm with one tack in front of and one behind the elbow joint of the affected limb. An incision of the skin was made in the middle of the upper left arm of the rat to expose and then bluntly separate the nerve. In the sham operation group and epineurial neurorrhaphy group, the median nerves were directly stimulated. In the musculocutaneous nerve transposition, medial pectoral nerve transposition, and radial nerve muscular branch transposition groups, a site 5 mm from the sleeve suture was stimulated with a Synergy electrophysiologic apparatus (Medelec Synergy; Oxford Instrument Inc., United Kingdom) with 0.9 mA continuous square waves at 50 Hz. The position of each left front paw was recorded with a digital camera (Sony, Tokyo, Japan) before and after stimulation. Results were synthesized with Image Pro Plus 4.5 software (Media Cybernetics, Silver Spring, MD, USA), and the angle of wrist flexion was measured.
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4

Wound Healing Measurement via Digital Imaging

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At 7, 14 and 21 days after grafting, wounds were photographed using a digital camera (Sony, Tokyo, Japan) and the rate of wound healing was calculated using Image-Pro Plus 6.0 image analysis software (Media Cybernetics, Rockville, MD, USA):

When the majority of the graft was absorbed and tightly combined with the surrounding wound, this was considered as healed.
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5

Imaging Arabidopsis Floral Structures

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Individual Arabidopsis floral structure, and floral buds and siliques were photographed using a solid microscope (Olympus, Tokyo, Japan). Morphology of the Arabidopsis roots and plants was photographed using a digital camera (Sony, Tokyo, Japan).
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6

Histomorphometric Analysis of Bone Samples

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After decalcification and fitting into paraffin blocks, samples were cut using a microtome. Multiple serial sections were prepared for the analysis of each tissue sample. Histomorphometry was performed using a light microscope (Olympus BHA, Tokyo, Japan) to which a digital camera (Sony, Yokohama, Japan) was adapted. Magnification was 40×. Microphotographs of histological sections were transferred to the monitor of the computer software for quantitative analysis of the microscopic images (VAMS, Zagreb, Croatia), and the parameter values were quantified as follows: bone volume/total volume, BV/TV (%), and residual biomaterial/total volume, RB (%).
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7

Cutaneous Wound Healing in Mice

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The rate of skin wound closure following injury was determined using a cutaneous wound healing model. Mice were anesthetized with 1.5-2 % isoflurane and the dorsal skin was shaved and cleaned with alcohol. Per mouse, one bilateral full-thickness skin wound were created, using a sterile 3 mm biopsy punch on the dorsorostral back skin without injuring the underlying muscle. Wounds were digitally photographed at 0, 4, and 7 days after injury using a digital camera (Sony Europe Limited, Weybridge, UK).
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8

Immunohistological Analysis of Neuroinflammation

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The paraffin blocks were cut into 4 μm slices using a microtome, placed in polysine slides and heated to 56–58 °C overnight. The activity of endogen peroxide was eliminated by incubating the slides in 3% hydrogen peroxide for 30 min at room temperature. The slides were deparaffinated in xylol for five minutes and washed with tap water four times, rehydrated in 95% alcohol for five minutes, 70% alcohol for five minutes and, finally, washed with tap water for five minutes. The slides were immunohistologically stained using monoclonal antibody, anti-rat anti-Nav1.7 (CST, USA), anti-HSP70 (SantaCruz Biotech. USA) and anti-TNFα (SantaCruz Biotech. USA), before being counterstained with Haematoxylin Meyer (Pizem and Coem, 2003 , Soini et al., 1998 (link)). The expression of Nav1.7 in the pulp neuron cell and that of HSP70 and TNFα in the macrophage cells were observed under a light microscope (Nikon, Japan) at 1000× magnification, with pictures taken using a digital camera (Sony, USA).
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9

Fluorescent Imaging of Fish Samples

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All of the fish samples were observed under a microscope (DM 2500, Leica; Buffalo Grove, NY, USA) equipped with a fluorescent DsRed filter cube (Kramer Scientific, Amesbury, MA, USA), and we captured pictures of the fish at particular stages using a digital camera (Sony, Tokyo, Japan).
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10

Automated Histological Image Analysis

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After HE staining or histochemical staining of sections from six mice of each genotype, images of fields were photographed with a Sony digital camera. All images were digitally recorded using a rectangular template, and recordings were processed and analyzed using Northern Eclipse image analysis software as described [23] (link), [26] (link), [28] (link).
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