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Masson trichrome staining kit

Manufactured by Beyotime
Sourced in China

The Masson trichrome staining kit is a lab equipment used for staining biological samples. It is designed to differentiate collagen, muscle, and other connective tissues by staining them in different colors.

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3 protocols using masson trichrome staining kit

1

Histological Analysis of Lung Tissue

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Lung tissue was fixed with 4% polyformaldehyde solution for 24 h, dehydrated and paraffin embedded and cut into 4-μm slices. Then, the slices (3 slices per mouse) were stained with hematoxylin and eosin (H&E) to observe histopathological changes in the colon under a microscope. Masson trichrome staining was performed using Masson trichrome staining kit (Beyotime, China). Histological sections were stained with hematoxylin and eosin (H&E) to assess histopathological changes, and Masson trichrome staining was performed following the manufacturer's instructions.
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2

Masson's Trichrome Staining of PFA-fixed Tissues

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Paraffin-embedded sections of PFA-fixed tissues were dewaxed and hydrated. Staining was then performed using a Masson trichrome staining kit (Beyotime, China). In brief, the sections were dipped in Bouin buffer for 2 hours at 37°C and then successively stained with Celestine blue staining solution, hematoxylin staining solution, Ponceau S staining solution, and aniline blue solution for 3 min. After dehydrating with ethyl alcohol three times, the sections were mounted with Neutral Balsam Mounting Medium (BBI Life Science, China). Images were captured under a Zeiss LSM 880 confocal microscope.
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3

Histological Analysis of Rat Myocardial Tissue

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Rat hearts were collected, and myocardial tissue was washed with normal saline. Then, we used 4% paraformaldehyde to fix myocardial tissue. We used gradient alcohol for dehydration and embed myocardial tissue in paraffin. Then, we used a microtome to make paraffin blocks into paraffin sections. Before hematoxylin-eosin (HE) staining, we put paraffin slices in xylene and gradient alcohol for dewaxing and hydration. Then, we stained the cell nucleus with hematoxylin solution (Beyotime, Shanghai, China) for 1 minute. After rinsing slices with running water, we used 1% hydrochloric acid alcohol for differentiation. Then, we used eosin solution (Beyotime, Shanghai, China) to stain the cytoplasm. Finally, we used neutral gum for sealing. In addition, we used Masson trichrome staining kit (Beyotime, Shanghai, China) for staining according to the manufacturer's instructions. Collagen fibers appear blue and muscles appear red.
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