masson s trichrome stain kit (Servicebio Inc)

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Servicebio Inc masson s trichrome stain kit

In vivo atherosclerosis reversal. ( A ) Schematic illustration of the experimental timeline and treatment strategy for establishing a mature, vulnerable atherosclerosis model and evaluating therapeutic interventions. Mice were fed a high-fat diet (HFD) for 12 weeks and then divided into five groups (HFD+ 12W, Saline HFD+, OPN-HMCN@MLT HFD+, Saline HFD−, and OPN-HMCN@MLT HFD−). Except for the HFD+ 12W group, the remaining groups were further maintained for an additional 4 weeks under either HFD or non-HFD conditions with the indicated treatments. ( B , C ) Images of en face ORO-stained aortas ( B ) and quantitative analysis of ORO-positive regions ( C ) from mice subjected to different treatments and diets (n = 6, scale bar: 5 mm). ( D ) Aortic root sections stained by ORO, H&E, α-SMA <t>antibody,</t> <t>Masson's</t> trichrome, CD68 antibody, and MMP-9 antibody, respectively, following various therapeutic procedures (n = 6, scale bar: 500 μm). ( E - J ) Quantitative data of lipid accumulation ( E ), necrotic core area ( F ), collagen area ( G ), MMP-9 level ( H ), VSMC area ( I ), and macrophage-foam cell area ( J ) in aortic root sections. ( K ) Vulnerability scores of aortic root plaque. ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001, ∗∗∗∗ P < 0.0001.

Masson S Trichrome Stain Kit, supplied by Servicebio Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/staining+kit/masson+s/pmc12969391-56-5-12
Average 86 stars, based on 1 article reviews

masson s trichrome stain kit - by Bioz Stars, 2026-10

86/100 stars

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1) Product Images from "A foam cell-targeted lipophagy restoration strategy stabilizes vulnerable atherosclerotic plaques"

Article Title: A foam cell-targeted lipophagy restoration strategy stabilizes vulnerable atherosclerotic plaques

Journal: Bioactive Materials

doi: 10.1016/j.bioactmat.2026.02.041

Figure Legend Snippet: In vivo atherosclerosis reversal. ( A ) Schematic illustration of the experimental timeline and treatment strategy for establishing a mature, vulnerable atherosclerosis model and evaluating therapeutic interventions. Mice were fed a high-fat diet (HFD) for 12 weeks and then divided into five groups (HFD+ 12W, Saline HFD+, OPN-HMCN@MLT HFD+, Saline HFD−, and OPN-HMCN@MLT HFD−). Except for the HFD+ 12W group, the remaining groups were further maintained for an additional 4 weeks under either HFD or non-HFD conditions with the indicated treatments. ( B , C ) Images of en face ORO-stained aortas ( B ) and quantitative analysis of ORO-positive regions ( C ) from mice subjected to different treatments and diets (n = 6, scale bar: 5 mm). ( D ) Aortic root sections stained by ORO, H&E, α-SMA antibody, Masson's trichrome, CD68 antibody, and MMP-9 antibody, respectively, following various therapeutic procedures (n = 6, scale bar: 500 μm). ( E - J ) Quantitative data of lipid accumulation ( E ), necrotic core area ( F ), collagen area ( G ), MMP-9 level ( H ), VSMC area ( I ), and macrophage-foam cell area ( J ) in aortic root sections. ( K ) Vulnerability scores of aortic root plaque. ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001, ∗∗∗∗ P < 0.0001.

Techniques Used: In Vivo, Saline, Staining

In vivo anti-atherosclerosis effects. ( A ) Diagram illustrating the treatment protocol for apoE −/− mice. ( B , C ) En face ORO staining images and quantitative analysis of the lesion area of aortic lesion areas in apoE −/− mice following various treatments (n = 6, scale bar: 5 mm). ( D ) Quantification of the reduction ratio (versus model) of ORO-positive area to the entire aorta. ( E ) Cross-sectional images of ORO-stained aortic root (scale bars, 500 μm) and brachiocephalic artery (scale bars, 200 μm). n = 6. ( F and G ) Quantitative analysis of the aortic root lesion area ( F ) and the reduction ratio (versus model) of ORO-positive area to the aortic root ( G ). ( H ) Aortic root sections stained by H&E, α-SMA antibody, Masson's trichrome, CD68 antibody, MMP-9 antibody, and OPN antibody, respectively, following various therapeutic procedures (n = 6, scale bar: 500 μm). ( I-M ) Quantitative data of necrotic core area ( I ), collagen area ( J ), VSMC area ( K ), macrophage-foam cell area ( L ), and MMP-9 level ( M ) in aortic root sections. ( N ) Representative TEM images of LDs in the aortic root and arch of apoE −/− mice following various treatments (scale bar: 1 μm). The green arrow indicates elastic fibers. ( O-R ) Quantification of lipid droplet number and average area per cell section, n = 6. ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001, and ∗∗∗∗ P < 0.0001.

Figure Legend Snippet: In vivo anti-atherosclerosis effects. ( A ) Diagram illustrating the treatment protocol for apoE −/− mice. ( B , C ) En face ORO staining images and quantitative analysis of the lesion area of aortic lesion areas in apoE −/− mice following various treatments (n = 6, scale bar: 5 mm). ( D ) Quantification of the reduction ratio (versus model) of ORO-positive area to the entire aorta. ( E ) Cross-sectional images of ORO-stained aortic root (scale bars, 500 μm) and brachiocephalic artery (scale bars, 200 μm). n = 6. ( F and G ) Quantitative analysis of the aortic root lesion area ( F ) and the reduction ratio (versus model) of ORO-positive area to the aortic root ( G ). ( H ) Aortic root sections stained by H&E, α-SMA antibody, Masson's trichrome, CD68 antibody, MMP-9 antibody, and OPN antibody, respectively, following various therapeutic procedures (n = 6, scale bar: 500 μm). ( I-M ) Quantitative data of necrotic core area ( I ), collagen area ( J ), VSMC area ( K ), macrophage-foam cell area ( L ), and MMP-9 level ( M ) in aortic root sections. ( N ) Representative TEM images of LDs in the aortic root and arch of apoE −/− mice following various treatments (scale bar: 1 μm). The green arrow indicates elastic fibers. ( O-R ) Quantification of lipid droplet number and average area per cell section, n = 6. ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001, and ∗∗∗∗ P < 0.0001.

Techniques Used: In Vivo, Staining

Staining:

Article Title: Qishen paste improves cardiac conduction in heart failure by regulating cardiac resident macrophage Connexin43.
Article Snippet: Ethnopharmacological relevance: Heart failure (HF) is a complex clinical syndrome characterized by significant cardiac electrical conduction disturbances.. Qishen paste (QSP), a modern herbal formulation consisting of the dried root of Astragalus membranaceus (Fisch.). Bge. (Fabaceae), the dried root and rhizome of Salvia miltiorrhiza Bunge (Lamiaceae), the processed lateral root of Aconitum carmichaelii Debeaux (Ranunculaceae), the dried root of Scrophularia ningpoensis Hemsl. (Scrophulariaceae), the dried flower bud of Lonicera japonica Thunb. (Caprifoliaceae), and the dried root and rhizome of Glycyrrhiza uralensis Fisch. ex DC. (Fabaceae), has shown therapeutic efficacy in HF, but its mechanisms in regulating immune homeostasis and electrical conduction remain

Article Title: A biomimetic nanoplatform-reinforced hydrogel for multipronged STING suppression to remodel bone-immune homeostasis in diabetic periodontitis.
Article Snippet: The innate immune disorder caused by diabetes significantly aggravates bone destruction in periodontitis.. STING signaling is a critical target linking periodontal tissue damage and innate immune activation, yet related strategies remain scarce.. In this study, we developed a biomimetic nanoplatform composed of a zinc-procyanidin c80dination network that is encapsulated by an apoptotic neutrophil membrane and loaded with DNase I, and incorporated it into a reactive oxygen species (ROS)-responsive phenylboronic acid-modified poly(L-lysine) hydrogel system (NM-ZnPC@DNase/Gel).

Article Title: Lycorine Attenuates Cardiac Fibrosis Through the Regulation of PYK2 Expression and Activity.
Article Snippet: The upper part of the tissue containing the atria was cross-sectioned and immersed in 4% paraformaldehyde and fixed for 24 h. Samples were selected according to qPCR and WB results and submitted to AiFang Biological for embedding and sectioning. .. Masson staining kit was purchased from Servicebio, and the paraffin sections were dewaxed, stained, dehydrated, and sealed according to the manufacturer’s instructions, and then, the slides were scanned with a tissue scanner for a panoramic view of Col fibers in blue and myofibrils, fibrils, and erythrocytes in red. .. The quantitative analysis of the staining results was performed using ImageJ software.

Article Title: NAT10-mediated N4-acetylcytidine modification drives RNA splicing of PML to alleviate adipose-derived stem cell senescence and promote diabetic wound healing.
Article Snippet: .. The sections were stained using the H&E Staining Kit (Servicebio, G1076) and the Masson Stain Kit (Servicebio, G1006), according to the manufacturer’s protocol. .. Micrographs were captured using an Olympus light microscope.

Article Title: The cysteine metabolic regulation through CSE-transsulfuration pathway is essential in iron-induced oxidative damage of heart.
Article Snippet: .. The sections were stained using Hematoxylin and Eosin (H&E) staining kit (G1076, Servicebio) and Masson's trichrome staining kit (G1006, Servicebio) according to the manufacturers' instructions. ..

Article Title: A foam cell-targeted lipophagy restoration strategy stabilizes vulnerable atherosclerotic plaques
Article Snippet: Ox-LDL was obtained from Solarbio Science & Technology Co., Ltd. (Beijing, China). .. Oil Red O, Hematoxylin-Eosin, and Masson's Trichrome Stain Kit were purchased from Servicebio in Wuhan, China. .. 13 C-labeled palmitic acids were purchased commercially from Cambridge Isotope Laboratories.

Article Title: Epithelial cell expansion drives cyst progression in genetic models of autosomal recessive polycystic kidney disease
Article Snippet: .. Hemolytoxin and Eosin (H&E) staining and Masson’s trichrome staining were performed by Servicebio. ..

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