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Af s micro nikkor 60 mm f 2.8 g ed lens

Manufactured by Nikon
Sourced in Japan

The AF-S Micro Nikkor 60 mm f/2.8 G ED lens is a high-quality macro lens designed for Nikon DSLR cameras. It features a fast maximum aperture of f/2.8, which allows for shallow depth of field and low-light performance. The lens is equipped with Silent Wave Motor autofocus and Extra-low Dispersion glass elements for sharp, high-contrast images. It has a minimum focusing distance of 0.185 m (0.61 ft) and a magnification ratio of up to 1:1, making it suitable for close-up photography applications.

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5 protocols using af s micro nikkor 60 mm f 2.8 g ed lens

1

Evaluating Wound Healing in Mice

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The clinical condition of mice (e.g., total wound area, progress of healing process, skin inflammation intensity and mobility) was recorded daily. The animals were weighted periodically. Skin images for photo-documentation were acquired using a Nikon D5100 digital camera (Nikon, Tokyo, Japan) equipped with an AF-S Micro Nikkor 60 mm f/2.8 G ED lens (Nikon, Tokyo, Japan), which was at a fixed distance of 30 cm perpendicular to the subject. The photographs were digitized, and the wound area was measured using Adobe Photoshop C5. Wound closure was defined as a reduction in the wound area and the results were expressed as a percentage (%) of the original wound area.
At the end of the experiment, when total wound closure could be observed for at least one group of treated mice, the mice were sacrificed and skin tissue was excised. Skin sections of specimens from all groups were performed using a paraffin microtome (Shandon Finesse, Thermo Fisher Scientific, Cheshire, UK) and stained with hematoxylin and eosin stain kit (Atom Scientific, Cheshire, UK). Parameters such as inflammation, hyperkeratosis, parakeratosis and skin structure, were estimated.
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2

Imaging and Evaluating Wound Area

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Wounds were photographed after wound induction and every other day until the end of the experiments using a Nikon D5100 digital camera (Nikon, Tokyo, Japan) equipped with an AF-S Micro Nikkor 60 mm f/2.8 G ED lens (Nikon, Tokyo, Japan), which was fixed at a distance of 20 cm perpendicular to the subject. Pictures were also acquired using an Antera 3D camera (Miravex, Dublin, Ireland). Antera 3D uses an optical method combined with a complex algorithm to capture images in three dimensions. Its software, version 2.11.5, was used to evaluate wound area (mm2) and volume [28 (link)].
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3

Capturing Small-Bodied Herpetological Specimens

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A Nikon AF-S Micro-NIKKOR 60 mm f/2.8G ED lens was used to capture project specimens and can approach or achieve a 1:1 magnification ratio or greater for small-bodied specimens. Because reptile and amphibian subjects have wide-ranging body sizes, a 50–100 mm lens is recommended for capturing herpetological specimens with a wet imaging station setup.
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4

Murine Skin Inflammation Assessment

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The clinical condition of mice (e.g., skin inflammation intensity and mobility) was recorded daily. The animals were weighted at day 1, 4, 7 and 10. Skin images for photo-documentation were acquired using a Nikon D5100 digital camera (Nikon, Tokyo, Japan) equipped with a AF-S Micro Nikkor 60 mm f/2.8 G ED lens (Nikon, Tokyo, Japan), which was at a fixed distance of 33 cm perpendicular to the subject.
At the end of the experiment, which lasted for 10 days when no inflammation could be observed for at least one group of treated mice, the mice were sacrificed and skin tissue was excised. Skin sections of specimens from all groups were performed using a paraffin microtome (Shandon Finesse, Thermo Scientific, USA) and stained with haematoxylin & eosin stain kit (Atom Scientific, Cheshire, UK). Parameters such as inflammation, hyperkeratosis, parakeratosis and skin structure, were estimated.
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5

Hypocotyl Growth Quantification

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To determine the growth rate of the hypocotyl, after stratification, the boxes were turned to place with the agar vertically. The seedlings were photographed from their side on a fixed support with a digital camera (Nikon D5600 with the AF-S Micro-Nikkor 60 mm f/2.8 G ED lens) at the beginning of treatment and at the end of the photoperiod of that day (unless otherwise indicated). The length of each hypocotyl was measured with Fiji (72 (link)) at each time point, and the difference was calculated and divided by the number of hours between successive measurements to calculate the growth rate. In cotyledon growth experiments, the agar remained at the horizontal position throughout the experiments, and the seedlings were photographed from above. In experiments involving different nitrate (or nitrogen) treatments applied only to the wild type, each biological replicate is the pooled data of all the seedlings of the growth box. In experiments comparing the response to nitrate of different genotypes, each seedling is a replicate because all the genotypes were in the same growth box.
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