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Microfocus x ray ct system smx 90ct

Manufactured by Shimadzu
Sourced in Japan

The Microfocus X-ray CT system SMX-90CT is a laboratory instrument designed for high-resolution computed tomography (CT) imaging. It utilizes X-ray technology to generate detailed three-dimensional (3D) images of various samples. The system is capable of analyzing the internal structure and composition of a wide range of materials, including metals, ceramics, and polymers.

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2 protocols using microfocus x ray ct system smx 90ct

1

Skeletal Staining and Imaging Protocol

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Whole mount skeletons were stained with 0.05% alizarin red (A5533, Sigma-Aldrich) and 0.15% alcian blue 8GX (A5268, Sigma-Aldrich), and then transferred with glycerol/KOH solutions from 20% glycerol/1% KOH to 80% glycerol/1% KOH. For whole-mount lacZ staining, reporter mice were fixed in 1% formaldehyde and 0.2% glutaraldehyde in PBS for 90 min, stained in X-gal for 2 h at 37°C, and cleared in 80% glycerol/PBS. For histological analysis with alcian blue and von Kossa staining, sections were stained with 1% aqueous silver nitrate (196-00831, Fujifilm) solution and 1% alcian blue (pH 2.5, 8GX, Sigma-Aldrich) solutions. Unreacted silver was removed using 5% sodium thiosulfate. Counterstaining was performed using nuclear fast red staining. Micro-computed tomography (μCT) scanning of the harvested femurs was performed using a microfocus X-ray CT system SMX-90CT (Shimadzu, Kyoto, Japan); the three-dimensional construction software package TRI/3D-BON (Ratoc System Engineering, Tokyo) was used for quantitative analysis.
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2

Skeletal Staining and Imaging Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
Whole mount skeletons were stained with 0.05% alizarin red (A5533, Sigma-Aldrich) and 0.15% alcian blue 8GX (A5268, Sigma-Aldrich), and then transferred with glycerol/KOH solutions from 20% glycerol/1% KOH to 80% glycerol/1% KOH. For whole-mount lacZ staining, reporter mice were fixed in 1% formaldehyde and 0.2% glutaraldehyde in PBS for 90 min, stained in X-gal for 2 h at 37°C, and cleared in 80% glycerol/PBS. For histological analysis with alcian blue and von Kossa staining, sections were stained with 1% aqueous silver nitrate (196-00831, Fujifilm) solution and 1% alcian blue (pH 2.5, 8GX, Sigma-Aldrich) solutions. Unreacted silver was removed using 5% sodium thiosulfate. Counterstaining was performed using nuclear fast red staining. Micro-computed tomography (μCT) scanning of the harvested femurs was performed using a microfocus X-ray CT system SMX-90CT (Shimadzu, Kyoto, Japan); the three-dimensional construction software package TRI/3D-BON (Ratoc System Engineering, Tokyo) was used for quantitative analysis.
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