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picrosirius red staining solution  (Beijing Solarbio Science)


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    Beijing Solarbio Science picrosirius red staining solution
    Picrosirius Red Staining Solution, supplied by Beijing Solarbio Science, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/picrosirius+red+staining+solution/picro+sirius+red+staining/pm40325895-415-17-21
    Average 90 stars, based on 1 article reviews
    picrosirius red staining solution - by Bioz Stars, 2026-11
    90/100 stars

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    Article Title: Remodeling the Senescent Microenvironment for Promoting Osteoporotic Tendon-to-Bone Healing via Synergizing Senolytic Quercetin and Aligned Nanowire-Structured Hydrogels.
    Article Snippet: Osteoporotic tendon-to-bone healing remains a major challenge, as cellular senescence disrupts tissue regeneration and impairs repair outcomes.. Although the role of cellular senescence in rotator cuff repair is increasingly recognized, current strategies often overlook the complex pathological context, particularly the dual impacts of senescence on both bone marrow-derived mesenchymal stem cells (BMSCs) and tendon-derived stem cells (TDSCs).. This gap hampers effective tendon-to-bone healing and integration, especially under osteoporotic conditions.



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    Myocardial interstitial fibrosis in offspring on postnatal day 7. ( A ) Representative images of Masson’s trichrome-stained transverse cardiac sections in neonatal offspring; areas positive for collagen were stained blue. ( B ) Representative images of ventricular mid-cardiac sections stained with <t>picrosirius</t> red and polarized light detection in offspring: areas positive for collagen were stained red in picrosirius red staining, areas positive for collagen type I were stained yellow, and collagen type III areas were stained green in the polarized light detection. ( C , D ) Representative images of collagen type I and collagen type III immunohistochemical-stained transverse cardiac sections in offspring. ( E ) Quantification of total fibrosis expressed as a percentage of tissue area by Masson’s trichrome staining ( n = 5). ( F , G ) Collagen type I and collagen type III expression score (H-score) in transverse cardiac sections using immunohistochemical staining ( n = 3). Bar = 20 μm. *** p < 0.001, ** p < 0.01, * p < 0.05.
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    Myocardial interstitial fibrosis in offspring on postnatal day 7. ( A ) Representative images of Masson’s trichrome-stained transverse cardiac sections in neonatal offspring; areas positive for collagen were stained blue. ( B ) Representative images of ventricular mid-cardiac sections stained with <t>picrosirius</t> red and polarized light detection in offspring: areas positive for collagen were stained red in picrosirius red staining, areas positive for collagen type I were stained yellow, and collagen type III areas were stained green in the polarized light detection. ( C , D ) Representative images of collagen type I and collagen type III immunohistochemical-stained transverse cardiac sections in offspring. ( E ) Quantification of total fibrosis expressed as a percentage of tissue area by Masson’s trichrome staining ( n = 5). ( F , G ) Collagen type I and collagen type III expression score (H-score) in transverse cardiac sections using immunohistochemical staining ( n = 3). Bar = 20 μm. *** p < 0.001, ** p < 0.01, * p < 0.05.
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    Myocardial interstitial fibrosis in offspring on postnatal day 7. ( A ) Representative images of Masson’s trichrome-stained transverse cardiac sections in neonatal offspring; areas positive for collagen were stained blue. ( B ) Representative images of ventricular mid-cardiac sections stained with <t>picrosirius</t> red and polarized light detection in offspring: areas positive for collagen were stained red in picrosirius red staining, areas positive for collagen type I were stained yellow, and collagen type III areas were stained green in the polarized light detection. ( C , D ) Representative images of collagen type I and collagen type III immunohistochemical-stained transverse cardiac sections in offspring. ( E ) Quantification of total fibrosis expressed as a percentage of tissue area by Masson’s trichrome staining ( n = 5). ( F , G ) Collagen type I and collagen type III expression score (H-score) in transverse cardiac sections using immunohistochemical staining ( n = 3). Bar = 20 μm. *** p < 0.001, ** p < 0.01, * p < 0.05.
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    Male and female wild-type (WT) and seipin knockout (SKO) mice were intraperitoneally injected once daily with phosphate-buffered saline (PBS) or 0.2 mg/kg liraglutide (Lira) for 14 days. ( A ) Liver weight normalised to mice body weight. ( B ) Levels of hepatic triglycerides. ( C, D ) Representative images of hematoxylin and eosin (H&E) and <t>picrosirius</t> red-stained paraffin-embedded liver sections along with representative photographs of macroscopic liver appearance in female ( C ) and male ( D ) mice. Bars denote 200 µm. ( E, F ) Expression levels of a panel of fibrosis markers genes in WT mice and SKO mice treated with PBS or liraglutide. Gene expression was normalised to three reference genes ( Hprt, Nono and Ywhaz ) (female n= 6-7, male n= 8-10). Data are presented as mean ± SEM; *p < 0.05, **p < 0.01, ***p < 0.001 (PBS versus liraglutide within same genotype); # p < 0.05, ## p < 0.01, ### p < 0.001, #### p < 0.0001 (WT (PBS) versus SKO (PBS)).
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    Danaher Inc picrosirius red psr staining
    (A) Representative cross sections of H&E and <t>picrosirius</t> red stained tissue 1 day and 28 days after MVF implantation (scale = 500 μm). (B) Rectangularity measurements of implanted MVF. (C) Representative close-up image from WGA-stained muscles (scale = 50 μm). (D) Muscle fiber count of muscles with MVF implantation 1 day and 28 days after implantation. Dotted line and shaded region represents the mean ± SD for fiber number from healthy tibialis anterior muscles. (E) Kernel density estimations of the distribution of minimum Feret diameters 1 and 28 days after MVF implantation. Data in panels B and D were analyzed first via a 2-way ANOVA followed by Holm-Sidak post hoc test. Median data in panel E were analyzed via Kruskal-Wallis test. Post hoc p-values less than 0.05 are listed for all comparisons. Data represented as mean ± SD. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
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    Image Search Results


    Myocardial interstitial fibrosis in offspring on postnatal day 7. ( A ) Representative images of Masson’s trichrome-stained transverse cardiac sections in neonatal offspring; areas positive for collagen were stained blue. ( B ) Representative images of ventricular mid-cardiac sections stained with picrosirius red and polarized light detection in offspring: areas positive for collagen were stained red in picrosirius red staining, areas positive for collagen type I were stained yellow, and collagen type III areas were stained green in the polarized light detection. ( C , D ) Representative images of collagen type I and collagen type III immunohistochemical-stained transverse cardiac sections in offspring. ( E ) Quantification of total fibrosis expressed as a percentage of tissue area by Masson’s trichrome staining ( n = 5). ( F , G ) Collagen type I and collagen type III expression score (H-score) in transverse cardiac sections using immunohistochemical staining ( n = 3). Bar = 20 μm. *** p < 0.001, ** p < 0.01, * p < 0.05.

    Journal: Nutrients

    Article Title: Promoting Glutathione Synthesis: A Possibility for Treating Cardiomyopathy Induced by a Maternal Western Diet

    doi: 10.3390/nu16152520

    Figure Lengend Snippet: Myocardial interstitial fibrosis in offspring on postnatal day 7. ( A ) Representative images of Masson’s trichrome-stained transverse cardiac sections in neonatal offspring; areas positive for collagen were stained blue. ( B ) Representative images of ventricular mid-cardiac sections stained with picrosirius red and polarized light detection in offspring: areas positive for collagen were stained red in picrosirius red staining, areas positive for collagen type I were stained yellow, and collagen type III areas were stained green in the polarized light detection. ( C , D ) Representative images of collagen type I and collagen type III immunohistochemical-stained transverse cardiac sections in offspring. ( E ) Quantification of total fibrosis expressed as a percentage of tissue area by Masson’s trichrome staining ( n = 5). ( F , G ) Collagen type I and collagen type III expression score (H-score) in transverse cardiac sections using immunohistochemical staining ( n = 3). Bar = 20 μm. *** p < 0.001, ** p < 0.01, * p < 0.05.

    Article Snippet: Subsequently, the sections were incubated in a picrosirius red staining solution (ab246832, Abcam, Boston, MA, USA) for one hour.

    Techniques: Staining, Immunohistochemical staining, Expressing

    Male and female wild-type (WT) and seipin knockout (SKO) mice were intraperitoneally injected once daily with phosphate-buffered saline (PBS) or 0.2 mg/kg liraglutide (Lira) for 14 days. ( A ) Liver weight normalised to mice body weight. ( B ) Levels of hepatic triglycerides. ( C, D ) Representative images of hematoxylin and eosin (H&E) and picrosirius red-stained paraffin-embedded liver sections along with representative photographs of macroscopic liver appearance in female ( C ) and male ( D ) mice. Bars denote 200 µm. ( E, F ) Expression levels of a panel of fibrosis markers genes in WT mice and SKO mice treated with PBS or liraglutide. Gene expression was normalised to three reference genes ( Hprt, Nono and Ywhaz ) (female n= 6-7, male n= 8-10). Data are presented as mean ± SEM; *p < 0.05, **p < 0.01, ***p < 0.001 (PBS versus liraglutide within same genotype); # p < 0.05, ## p < 0.01, ### p < 0.001, #### p < 0.0001 (WT (PBS) versus SKO (PBS)).

    Journal: bioRxiv

    Article Title: GLP-1 Receptor Agonist Improves Metabolic Disease in a Pre-clinical Model of Lipodystrophy

    doi: 10.1101/2023.09.01.555852

    Figure Lengend Snippet: Male and female wild-type (WT) and seipin knockout (SKO) mice were intraperitoneally injected once daily with phosphate-buffered saline (PBS) or 0.2 mg/kg liraglutide (Lira) for 14 days. ( A ) Liver weight normalised to mice body weight. ( B ) Levels of hepatic triglycerides. ( C, D ) Representative images of hematoxylin and eosin (H&E) and picrosirius red-stained paraffin-embedded liver sections along with representative photographs of macroscopic liver appearance in female ( C ) and male ( D ) mice. Bars denote 200 µm. ( E, F ) Expression levels of a panel of fibrosis markers genes in WT mice and SKO mice treated with PBS or liraglutide. Gene expression was normalised to three reference genes ( Hprt, Nono and Ywhaz ) (female n= 6-7, male n= 8-10). Data are presented as mean ± SEM; *p < 0.05, **p < 0.01, ***p < 0.001 (PBS versus liraglutide within same genotype); # p < 0.05, ## p < 0.01, ### p < 0.001, #### p < 0.0001 (WT (PBS) versus SKO (PBS)).

    Article Snippet: Liver tissue and pancreata were fixed in 10% neutral buffered formalin, paraffin-embedded and 5 µm-thick sections were stained with hematoxylin and eosin (H&E) or picrosirius red solution (Abcam #ab150681) as in [ ].

    Techniques: Knock-Out, Injection, Saline, Staining, Expressing

    (A) Representative cross sections of H&E and picrosirius red stained tissue 1 day and 28 days after MVF implantation (scale = 500 μm). (B) Rectangularity measurements of implanted MVF. (C) Representative close-up image from WGA-stained muscles (scale = 50 μm). (D) Muscle fiber count of muscles with MVF implantation 1 day and 28 days after implantation. Dotted line and shaded region represents the mean ± SD for fiber number from healthy tibialis anterior muscles. (E) Kernel density estimations of the distribution of minimum Feret diameters 1 and 28 days after MVF implantation. Data in panels B and D were analyzed first via a 2-way ANOVA followed by Holm-Sidak post hoc test. Median data in panel E were analyzed via Kruskal-Wallis test. Post hoc p-values less than 0.05 are listed for all comparisons. Data represented as mean ± SD. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Journal: Materials Today Bio

    Article Title: In situ forming biomaterials as muscle void fillers for the provisional treatment of volumetric muscle loss injuries

    doi: 10.1016/j.mtbio.2023.100781

    Figure Lengend Snippet: (A) Representative cross sections of H&E and picrosirius red stained tissue 1 day and 28 days after MVF implantation (scale = 500 μm). (B) Rectangularity measurements of implanted MVF. (C) Representative close-up image from WGA-stained muscles (scale = 50 μm). (D) Muscle fiber count of muscles with MVF implantation 1 day and 28 days after implantation. Dotted line and shaded region represents the mean ± SD for fiber number from healthy tibialis anterior muscles. (E) Kernel density estimations of the distribution of minimum Feret diameters 1 and 28 days after MVF implantation. Data in panels B and D were analyzed first via a 2-way ANOVA followed by Holm-Sidak post hoc test. Median data in panel E were analyzed via Kruskal-Wallis test. Post hoc p-values less than 0.05 are listed for all comparisons. Data represented as mean ± SD. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Article Snippet: Picrosirius red (PSR) staining was performed with PSR kit (Abcam, ab150681) per the manufacturer's protocol.

    Techniques: Staining, Muscles

    (A) Color deconvolution of picrosirius red stained sections to isolate stained collagen. Zones of 25 μm thickness were made radiating out from the MVF-muscle border, pseudo-colored, and percent area of zone that consisted of collagen was quantified. Graph's dotted line and shaded region represents the mean ± SD for area of collagen in a healthy tibialis anterior muscle. *p < 0.05 for silicone vs PVA and silicone vs HA + PEG. (Scale = 500 μm) (B) Nuclei stained with DAPI and zones of 25 μm thickness were pseudo-colored and percent area of zone that consisted of positive DAPI signal was quantified (Scale = 50 μm). (C) Pan-macrophage marker CD68 was stained to look at cellular infiltrate. Analysis of total CD68 signal in cross section was quantified (Scale = 50 μm). All data were analyzed first via a 1 or 2-way ANOVA followed by Holm-Sidak post hoc test. Post hoc p-values less than 0.05 are listed for all comparisons. Data represented as mean ± SD. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Journal: Materials Today Bio

    Article Title: In situ forming biomaterials as muscle void fillers for the provisional treatment of volumetric muscle loss injuries

    doi: 10.1016/j.mtbio.2023.100781

    Figure Lengend Snippet: (A) Color deconvolution of picrosirius red stained sections to isolate stained collagen. Zones of 25 μm thickness were made radiating out from the MVF-muscle border, pseudo-colored, and percent area of zone that consisted of collagen was quantified. Graph's dotted line and shaded region represents the mean ± SD for area of collagen in a healthy tibialis anterior muscle. *p < 0.05 for silicone vs PVA and silicone vs HA + PEG. (Scale = 500 μm) (B) Nuclei stained with DAPI and zones of 25 μm thickness were pseudo-colored and percent area of zone that consisted of positive DAPI signal was quantified (Scale = 50 μm). (C) Pan-macrophage marker CD68 was stained to look at cellular infiltrate. Analysis of total CD68 signal in cross section was quantified (Scale = 50 μm). All data were analyzed first via a 1 or 2-way ANOVA followed by Holm-Sidak post hoc test. Post hoc p-values less than 0.05 are listed for all comparisons. Data represented as mean ± SD. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Article Snippet: Picrosirius red (PSR) staining was performed with PSR kit (Abcam, ab150681) per the manufacturer's protocol.

    Techniques: Staining, Marker