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Dm750p

Manufactured by Leica
Sourced in Germany

The DM750P is a monocular microscope designed for routine laboratory applications. It features a high-intensity LED illumination system and a range of optical objectives to enable clear, detailed observation of samples. The core function of the DM750P is to provide a reliable and efficient tool for magnifying and examining specimens in a laboratory setting.

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19 protocols using dm750p

1

Hematoxylin and Eosin Tissue Staining

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Tissue sections were decolorized with xylene and ethanol, and stained with hematoxylin to stain the nucleus. The excess hematoxylin was removed by washing in tap water, and then the cytoplasm was stained with eosin. Representative images of HE staining were captured using an optical microscope (Leica, DM750P).
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2

Fossil Specimen Imaging and Analysis

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Fossils specimens were photographed using a digital camera (D3X-Nikon with Nikon Micro-Nikkor 60 mm lens) and measured (lengths, distances, angles) from high-resolution digital images by using Image J, a public domain processing program. Polished and lithological thin sections were made using standard methods and observed under binocular stereo-microscope (Leica MZ125 and Leica DM750P). Elemental maps were acquired using a Tornado M4 micro-XRF system (Bruker, Germany) equipped with a silicon drift detector and a Rh source operating at 50 kV and 600 µA. A spot size of 40 µm was employed with dwell times of 7 ms/pixel, and mapping was performed under vacuum. Image processing included spectral deconvolution and 3-pixel averaging. Tomographic images of ROMIP 57013 were obtained via the same methods and with the same machine as in Kouraiss et al.69 (link).
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3

Imaging Cylindrical Micro-Structures

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For cross-sectional images the tubes were sectioned into thin segments of approximately 1 mm thickness cut perpendicular to the tube’s long axis. The images of the tube’s walls were obtained after sectioning along the tube’s long axis. The samples were placed in glass bottom 35 mm-dishes (MatTek Corporation, P35G-1.5-14-C) filled with milliΩ water. The samples were then imaged in between two perpendicular light polarizers using a Leica DM750 P instrument in reflection mode with a ×4 magnification using Leica Application Suite V4.2 software. A sample stage allowed for the precise rotation and x, y-positioning of the samples. Cross-sectional images were stitched using the ImageJ plugin tools “MosaicJ” and Grid/Collection Stitching by Preibisch et al41 (link). Bright-field images were recorded using the same instrument without the light polarizers.
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4

Surface Morphology and Anisotropy Analysis

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The specimens’ surface morphology was observed under a SEM (Hitachi S‐4800) at 10 kV. The anisotropy structure was observed using a POM (Leica DM750P) with a 0°/90° crossed polarizer analyzer.
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5

Characterization of self-made cement and dolomitic rocks

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X-ray diffraction (Smart Lab, Rigaku, Tokyo, Japan) analysis was used for the composition of the self-made cement without K+, Na+, and Mg2+ and the composition of dolomitic rocks. The length changes of all specimens prepared by different aggregates were measured at different ages and the expansion ratio of all the specimens were calculated by the abovementioned formula. Each length change value used was the mean value of three replicate specimens. The morphologies of aggregate grains enriched dolomite selected from the microbars cured in TMAH solution were also observed by SEM (JEOL, JEM-6510, Tokyo, Japan) coupled with EDS analysis. Orthogonal polarized light microscopy (DM750P, Leica, Germany) was also used to investigate the cracks as a result of ACR.
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6

Petrographic Analysis of Thin Sections

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Thin sections for optical microscopy and electron microprobe analysis were prepared by National Petrographic Services, Houston, Texas, using standard procedures. Initial observations were made with an Optima ZM-160AT dissecting scope and an Ernst Leitz Wetzlar light microscope; traditional petrographic observations were made with an Olympus BH2 and Leica DM750P in normal, polarized, and cross-polarized light.
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7

Coral Histological Preparation Methodology

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Coral samples growing on a coverslip are fixed overnight in 4% glutaraldehyde in artificial seawater buffered to pH 7.8 with 0.1 M sodium cacodylate (according to ref. 34 (link)). The samples were then rinsed in distilled water before being dehydrated through a series of ethanol solutions. The coral was then embedded in EPO-TEK® (Epoxy Technology, France) for sectioning. The sections (1.0 mm) were cut using the Minitom® and a diamond cut-off wheel Minitom® (Struers, France). The section was mounted on glass slides, polished using silicon carbide foils (up to 4000 grades, lubricated with water), and stained with toluidine blue in borax and photographed with a Leica DM750P.
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8

Characterization of AKD Emulsion Morphology

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The morphology of the AKD emulsions was observed using optical microscopy (Leica DM750P, Burladingen, Germany) and a HD camera (Leica MC170, Wetzlar, Germany) with a 20× objective lens. In addition, SEM was used to study the size and morphology of AKD emulsion—1.25% obtained after freeze drying.
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9

Optical Characterization of CLC-PUA Composites

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We examined the optical characteristics of the CLC prepolymer, the CLC template before and after the removal of residual unreactive materials, and the CLC-PUA composite films. A customized UV-vis. spectroscope (Ocean Optics) was used for measuring transmittance spectra. A polarized optical microscope (POM) (Leica, DM750P) was used for capturing the surface morphology and colors of the CLC-PUA composite film.
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10

Microscopic Characterization of Samples

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A stereo microscope Leica M 60 was used for the observation of bulk samples and a Leica DM750 P in both plane and polarised light mode was used for observing the thin section. SEM‐EDX observation (BSE images) and point analyses were performed with a QUANTA 2003D and EDX system from EDAX company.
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