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eyeball fixative solution mouse  (Servicebio Inc)

 
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    Servicebio Inc eyeball fixative solution mouse
    Eyeball Fixative Solution Mouse, 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/mouse+fix/fixative+solution/pm41512470-84-0-7
    Average 86 stars, based on 1 article reviews
    eyeball fixative solution mouse - by Bioz Stars, 2026-10
    86/100 stars

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    Related Articles

    Staining:

    Article Title: From Pathway Tracing to Actionable Targets: Integrative Mendelian Randomization and Experimental Triangulation Map Metabolic Pathways Across Ovarian Cancer Histotypes.
    Article Snippet: .. At the endpoint, the medium was discarded, cells were gently washed with PBS, fixed with fixative solution (Servicebio, G1101, Wuhan, China) for 15–30 min, and stained with crystal violet solution (Servicebio, G1014, Wuhan, China) for 10–20 min. ..

    Article Title: Garin3 regulates sperm-oocyte fusion and male fertility.
    Article Snippet: Following incubation, sperm motility and kinematic parameters were AR TIC LE IN PR ES S © 2026 evaluated using computer-assisted sperm analysis (Hamilton Thorne IVOS II, Beverly, MA, USA). .. Hematoxylin and eosin (HE) staining and scanning electron microscopy For HE staining, mouse testes were fixed in a testes fixative solution (Servicebio, G1121). ..

    Electron Microscopy:

    Article Title: Garin3 regulates sperm-oocyte fusion and male fertility.
    Article Snippet: Following incubation, sperm motility and kinematic parameters were AR TIC LE IN PR ES S © 2026 evaluated using computer-assisted sperm analysis (Hamilton Thorne IVOS II, Beverly, MA, USA). .. Hematoxylin and eosin (HE) staining and scanning electron microscopy For HE staining, mouse testes were fixed in a testes fixative solution (Servicebio, G1121). ..

    Article Title: Dietary coated sodium selenite enhances muscle growth associated with mitochondrial function in sub-adult grass carp ( Ctenopharyngodon idellus )
    Article Snippet: .. The right dorsal muscle tissue (0.5 cm × 0.5 cm × 0.5 cm) was immediately soaked in muscle fixative solution (G1111-100 ML, Servicebio Technology Co., Ltd., Wuhan, Hubei, China) for histological observation and 2.5% glutaraldehyde solution for electron microscopy observation. ..

    other:

    Article Title: Developmental transition of brown adipose tissue from a thermogenic to a lipogenic phenotype in neonatal goats revealed by single-nucleus transcriptomics.
    Article Snippet: One portion of each PRAT sample was fixed in fixative solution (Servicebio, China), and another portion was immediately frozen in liquid nitrogen and stored at −80°C.

    Blocking Assay:

    Article Title: EXPRESS: Olfactory ensheathing cell transplantation targets macrophage extracellular traps and NKCC1 to alleviate pain after spinal cord injury.
    Article Snippet: Finally, sections were mounted onto gelatin-coated slides using an anti-fluorescence quenching mounting medium with DAPI (Beyotime, China), dried, and imaged under an upright fluorescence microscope. .. RAW 264.7 cells or OECs were fixed with 4% fixative solution (Servicebio, China) for 15 min and permeabilized with 0.1% Triton X-100 (Beyotime, China) for 10 min. After blocking with 5% BSA (solarbio, China) in PBS for 30 min at 37°C, samples were incubated overnight at 4°C with primary antibodies against NKCC1 (ab303518, 1:1000; Abcam, UK), CD68 (ab283654, 1:1000; Abcam, UK), H3Cit (68345-1-Ig, 1:5000; Proteintech, China), or p75^NTR (ab52987, 1:50, Abcam, UK). .. Cells were washed 3 times in PBS (1 min each) and then incubated for 30 min at 37 °C in the dark with either CoraLite594-conjugated goat anti-mouse IgG (SA00013-3, 1:250; Proteintech, China) or CoraLite488-conjugated goat anti-rabbit IgG antibodies (SA00013-2, 1:500; Proteintech, China).

    Incubation:

    Article Title: EXPRESS: Olfactory ensheathing cell transplantation targets macrophage extracellular traps and NKCC1 to alleviate pain after spinal cord injury.
    Article Snippet: Finally, sections were mounted onto gelatin-coated slides using an anti-fluorescence quenching mounting medium with DAPI (Beyotime, China), dried, and imaged under an upright fluorescence microscope. .. RAW 264.7 cells or OECs were fixed with 4% fixative solution (Servicebio, China) for 15 min and permeabilized with 0.1% Triton X-100 (Beyotime, China) for 10 min. After blocking with 5% BSA (solarbio, China) in PBS for 30 min at 37°C, samples were incubated overnight at 4°C with primary antibodies against NKCC1 (ab303518, 1:1000; Abcam, UK), CD68 (ab283654, 1:1000; Abcam, UK), H3Cit (68345-1-Ig, 1:5000; Proteintech, China), or p75^NTR (ab52987, 1:50, Abcam, UK). .. Cells were washed 3 times in PBS (1 min each) and then incubated for 30 min at 37 °C in the dark with either CoraLite594-conjugated goat anti-mouse IgG (SA00013-3, 1:250; Proteintech, China) or CoraLite488-conjugated goat anti-rabbit IgG antibodies (SA00013-2, 1:500; Proteintech, China).



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    mouse xl cytokine array  (R&D Systems)
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    (A) Volcano plot summarizing results of whole liver <t>transcriptome</t> analysis of wild-type ( n = 6, 3 females) versus Dp16 ( n = 6, 3 females) mice. Significantly differentially expressed (q < 0.1) genes are colored in red. (B) Bar plot summarizing the results of gene set enrichment analysis of gene expression changes data in (A). (C) Heatmap showing the median Z score of the top 10 leading-edge genes from the epithelial-mesenchymal transition gene set. (D) Sina plots displaying the normalized relative expression (RPKM) of Col1a1 and Eln in wild-type and Dp16 mice. (E) Uniform manifold approximation and projection (UMAP) plot of single-cell <t>RNA</t> sequencing (scRNA-seq) analysis of mouse liver, color coded by cell clusters identified using Seurat. (F) UMAP plot displaying differential cellular abundance of clusters from scRNA-seq analysis of mouse liver. Significant (false discovery rate [FDR] <0.1) clusters are colored by mean fold-change. (G) Sina plots showing the Dp16 versus wild-type abundance of hepatocyte cluster 1 and endothelial cell cluster 2 from scRNA-seq analysis of mouse liver. (H) UMAP plot displaying the epithelial-mesenchymal transition gene set normalized enrichment score (NES) for each cluster. (I) Bubble plot summarizing Col1a1 single-cell expression across clusters and animals, with color representing mean expression and size representing percent of cells with expression. (J) Sina plot displaying the normalized pseudobulk counts of Col1a1 expression within the stellate cell cluster in wild-type and Dp16 animals. (K) Representative images of multiplexed stained liver sections from wild-type and Dp16 mice where DAPI is stained in blue, desmin in red, and smooth muscle actin (SMA) in yellow. Sina plot showing number of desmin+ and SMA+ cells as a percentage of total cells in wild-type mice ( n = 6, 3 females) and Dp16 mice ( n = 6, 3 females). (L) Representative images of picrosirius-red-stained (PSR) liver sections from wild-type ( n = 8, 4 females) and Dp16 ( n = 7, 4 females) mice, imaged under polarized light. Sina plot shows the total percent positive PSR staining in wild-type and Dp16 liver. For (K and L), individual data are presented with a bar at the median, and the p value, as determined by a Mann-Whitney U test, is shown. Scale bars, 100 μm.
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    mouse hearts  (Thermo Fisher)
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    (A) Volcano plot summarizing results of whole liver <t>transcriptome</t> analysis of wild-type ( n = 6, 3 females) versus Dp16 ( n = 6, 3 females) mice. Significantly differentially expressed (q < 0.1) genes are colored in red. (B) Bar plot summarizing the results of gene set enrichment analysis of gene expression changes data in (A). (C) Heatmap showing the median Z score of the top 10 leading-edge genes from the epithelial-mesenchymal transition gene set. (D) Sina plots displaying the normalized relative expression (RPKM) of Col1a1 and Eln in wild-type and Dp16 mice. (E) Uniform manifold approximation and projection (UMAP) plot of single-cell <t>RNA</t> sequencing (scRNA-seq) analysis of mouse liver, color coded by cell clusters identified using Seurat. (F) UMAP plot displaying differential cellular abundance of clusters from scRNA-seq analysis of mouse liver. Significant (false discovery rate [FDR] <0.1) clusters are colored by mean fold-change. (G) Sina plots showing the Dp16 versus wild-type abundance of hepatocyte cluster 1 and endothelial cell cluster 2 from scRNA-seq analysis of mouse liver. (H) UMAP plot displaying the epithelial-mesenchymal transition gene set normalized enrichment score (NES) for each cluster. (I) Bubble plot summarizing Col1a1 single-cell expression across clusters and animals, with color representing mean expression and size representing percent of cells with expression. (J) Sina plot displaying the normalized pseudobulk counts of Col1a1 expression within the stellate cell cluster in wild-type and Dp16 animals. (K) Representative images of multiplexed stained liver sections from wild-type and Dp16 mice where DAPI is stained in blue, desmin in red, and smooth muscle actin (SMA) in yellow. Sina plot showing number of desmin+ and SMA+ cells as a percentage of total cells in wild-type mice ( n = 6, 3 females) and Dp16 mice ( n = 6, 3 females). (L) Representative images of picrosirius-red-stained (PSR) liver sections from wild-type ( n = 8, 4 females) and Dp16 ( n = 7, 4 females) mice, imaged under polarized light. Sina plot shows the total percent positive PSR staining in wild-type and Dp16 liver. For (K and L), individual data are presented with a bar at the median, and the p value, as determined by a Mann-Whitney U test, is shown. Scale bars, 100 μm.
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    Image Search Results


    Changes in the abundance and gene expression profile of leukocytes in Nodal Δ/Δ females. (A) t-SNE of all Ptprc + cells at the Nodal loxP/loxP (n=2) and Nodal Δ/Δ (n=2) maternal-fetal interface. (B) Proportion of cell types in each sample. Notably, the proportion of maternal neutrophils, non-classical monocytes and PAMM1a cells was significantly decreased in Nodal Δ/Δ females, while the proportion of M2 and PAMM2 cells was increased (FDR<0.05). (C) The number of significant differentially expressed genes (DEGs) (adjusted P-value<0.1) in all immune cell clusters at the d10.5 maternal-fetal interface between Nodal loxP/loxP and Nodal Δ/Δ females.

    Journal: Frontiers in Immunology

    Article Title: Single-cell RNA sequencing of leukocytes at the maternal-fetal interface in physiological and pathological Nodal-deficient pregnancies

    doi: 10.3389/fimmu.2026.1611813

    Figure Lengend Snippet: Changes in the abundance and gene expression profile of leukocytes in Nodal Δ/Δ females. (A) t-SNE of all Ptprc + cells at the Nodal loxP/loxP (n=2) and Nodal Δ/Δ (n=2) maternal-fetal interface. (B) Proportion of cell types in each sample. Notably, the proportion of maternal neutrophils, non-classical monocytes and PAMM1a cells was significantly decreased in Nodal Δ/Δ females, while the proportion of M2 and PAMM2 cells was increased (FDR<0.05). (C) The number of significant differentially expressed genes (DEGs) (adjusted P-value<0.1) in all immune cell clusters at the d10.5 maternal-fetal interface between Nodal loxP/loxP and Nodal Δ/Δ females.

    Article Snippet: Probe hybridization was performed on approximately 500,000 cells/sample using the Chromium Fixed RNA Mouse Transcriptome Kit (10X Genomics Cat. No. PN-1000497) following protocol # CG000527 .

    Techniques: Gene Expression

    (A) Volcano plot summarizing results of whole liver transcriptome analysis of wild-type ( n = 6, 3 females) versus Dp16 ( n = 6, 3 females) mice. Significantly differentially expressed (q < 0.1) genes are colored in red. (B) Bar plot summarizing the results of gene set enrichment analysis of gene expression changes data in (A). (C) Heatmap showing the median Z score of the top 10 leading-edge genes from the epithelial-mesenchymal transition gene set. (D) Sina plots displaying the normalized relative expression (RPKM) of Col1a1 and Eln in wild-type and Dp16 mice. (E) Uniform manifold approximation and projection (UMAP) plot of single-cell RNA sequencing (scRNA-seq) analysis of mouse liver, color coded by cell clusters identified using Seurat. (F) UMAP plot displaying differential cellular abundance of clusters from scRNA-seq analysis of mouse liver. Significant (false discovery rate [FDR] <0.1) clusters are colored by mean fold-change. (G) Sina plots showing the Dp16 versus wild-type abundance of hepatocyte cluster 1 and endothelial cell cluster 2 from scRNA-seq analysis of mouse liver. (H) UMAP plot displaying the epithelial-mesenchymal transition gene set normalized enrichment score (NES) for each cluster. (I) Bubble plot summarizing Col1a1 single-cell expression across clusters and animals, with color representing mean expression and size representing percent of cells with expression. (J) Sina plot displaying the normalized pseudobulk counts of Col1a1 expression within the stellate cell cluster in wild-type and Dp16 animals. (K) Representative images of multiplexed stained liver sections from wild-type and Dp16 mice where DAPI is stained in blue, desmin in red, and smooth muscle actin (SMA) in yellow. Sina plot showing number of desmin+ and SMA+ cells as a percentage of total cells in wild-type mice ( n = 6, 3 females) and Dp16 mice ( n = 6, 3 females). (L) Representative images of picrosirius-red-stained (PSR) liver sections from wild-type ( n = 8, 4 females) and Dp16 ( n = 7, 4 females) mice, imaged under polarized light. Sina plot shows the total percent positive PSR staining in wild-type and Dp16 liver. For (K and L), individual data are presented with a bar at the median, and the p value, as determined by a Mann-Whitney U test, is shown. Scale bars, 100 μm.

    Journal: Cell reports

    Article Title: Altered hepatic metabolism in Down syndrome

    doi: 10.1016/j.celrep.2025.116835

    Figure Lengend Snippet: (A) Volcano plot summarizing results of whole liver transcriptome analysis of wild-type ( n = 6, 3 females) versus Dp16 ( n = 6, 3 females) mice. Significantly differentially expressed (q < 0.1) genes are colored in red. (B) Bar plot summarizing the results of gene set enrichment analysis of gene expression changes data in (A). (C) Heatmap showing the median Z score of the top 10 leading-edge genes from the epithelial-mesenchymal transition gene set. (D) Sina plots displaying the normalized relative expression (RPKM) of Col1a1 and Eln in wild-type and Dp16 mice. (E) Uniform manifold approximation and projection (UMAP) plot of single-cell RNA sequencing (scRNA-seq) analysis of mouse liver, color coded by cell clusters identified using Seurat. (F) UMAP plot displaying differential cellular abundance of clusters from scRNA-seq analysis of mouse liver. Significant (false discovery rate [FDR] <0.1) clusters are colored by mean fold-change. (G) Sina plots showing the Dp16 versus wild-type abundance of hepatocyte cluster 1 and endothelial cell cluster 2 from scRNA-seq analysis of mouse liver. (H) UMAP plot displaying the epithelial-mesenchymal transition gene set normalized enrichment score (NES) for each cluster. (I) Bubble plot summarizing Col1a1 single-cell expression across clusters and animals, with color representing mean expression and size representing percent of cells with expression. (J) Sina plot displaying the normalized pseudobulk counts of Col1a1 expression within the stellate cell cluster in wild-type and Dp16 animals. (K) Representative images of multiplexed stained liver sections from wild-type and Dp16 mice where DAPI is stained in blue, desmin in red, and smooth muscle actin (SMA) in yellow. Sina plot showing number of desmin+ and SMA+ cells as a percentage of total cells in wild-type mice ( n = 6, 3 females) and Dp16 mice ( n = 6, 3 females). (L) Representative images of picrosirius-red-stained (PSR) liver sections from wild-type ( n = 8, 4 females) and Dp16 ( n = 7, 4 females) mice, imaged under polarized light. Sina plot shows the total percent positive PSR staining in wild-type and Dp16 liver. For (K and L), individual data are presented with a bar at the median, and the p value, as determined by a Mann-Whitney U test, is shown. Scale bars, 100 μm.

    Article Snippet: Fixed liver single cell suspensions were hybridized with the Next GEM Single Cell Fixed RNA Mouse Transcriptome Probe Kit (10X Genomics), according to manufacturer instructions, and loaded into a Chromium X (10X Genomics) microfluidics instrument to generate an oil emulsion with partitioned nanoliter-scale droplets, each ideally containing a barcoded gel bead and a single cell, along with enzyme Master Mix (10X Genomics) for probe pair ligation and gel bead primer barcode extension.

    Techniques: Gene Expression, Expressing, Single Cell, RNA Sequencing, Staining, MANN-WHITNEY

    (A) Heatmap showing the median Z score of the leading-edge genes from the IFN gamma response gene set from wild-type and Dp16 liver bulk transcriptome analysis. (B) Sina plot displaying relative expression (RPKM) of Cxcl9 in wild-type and Dp16 liver bulk transcriptome analysis. (C) UMAP plot displaying the IFN gamma response gene set normalized enrichment score (NES) for each cluster. (D) Bubble plot displaying the mean expression and the percent of cells per cluster expressing Cxcl9 in wild-type and Dp16 mice. (E) Sina plot displaying the log 2 of the normalized counts of Cxcl9 expression within endothelial cell cluster 1 in wild-type and Dp16 animals. (F) Representative images of H&E-stained liver sections from adult wild-type, Dp16, and Dp16 2xIFNRs mice. Scale bars, 100 μm. (G) Sina plots showing liver pathology scoring from adult wild-type ( n = 13, 6 females), Dp16 ( n = 12, 5 females), and Dp16 2xIFNRs ( n = 13, 7 females) mice. p values, determined by a Mann-Whitney U test, are shown. (H) Sina plot displaying the grams/deciliter of plasma albumin from adult wild-type ( n = 6, 4 females), Dp16 ( n = 6, 2 females), and Dp16 2xIFNRs ( n = 8, 1 female) mice. p values, as determined by a Mann-Whitney U test, are shown. (I) Heatmap displaying the median Z score of plasma bile acids in adult wild-type ( n = 9, 4 females), Dp16 ( n = 13, 6 females), and Dp16 2xIFNRs ( n = 10, 5 females) mice. For (B and E), Benjamini-Hochberg adjusted p value ( q value) are indicated. For (B, E, and G), individual data are presented with a bar at the median.

    Journal: Cell reports

    Article Title: Altered hepatic metabolism in Down syndrome

    doi: 10.1016/j.celrep.2025.116835

    Figure Lengend Snippet: (A) Heatmap showing the median Z score of the leading-edge genes from the IFN gamma response gene set from wild-type and Dp16 liver bulk transcriptome analysis. (B) Sina plot displaying relative expression (RPKM) of Cxcl9 in wild-type and Dp16 liver bulk transcriptome analysis. (C) UMAP plot displaying the IFN gamma response gene set normalized enrichment score (NES) for each cluster. (D) Bubble plot displaying the mean expression and the percent of cells per cluster expressing Cxcl9 in wild-type and Dp16 mice. (E) Sina plot displaying the log 2 of the normalized counts of Cxcl9 expression within endothelial cell cluster 1 in wild-type and Dp16 animals. (F) Representative images of H&E-stained liver sections from adult wild-type, Dp16, and Dp16 2xIFNRs mice. Scale bars, 100 μm. (G) Sina plots showing liver pathology scoring from adult wild-type ( n = 13, 6 females), Dp16 ( n = 12, 5 females), and Dp16 2xIFNRs ( n = 13, 7 females) mice. p values, determined by a Mann-Whitney U test, are shown. (H) Sina plot displaying the grams/deciliter of plasma albumin from adult wild-type ( n = 6, 4 females), Dp16 ( n = 6, 2 females), and Dp16 2xIFNRs ( n = 8, 1 female) mice. p values, as determined by a Mann-Whitney U test, are shown. (I) Heatmap displaying the median Z score of plasma bile acids in adult wild-type ( n = 9, 4 females), Dp16 ( n = 13, 6 females), and Dp16 2xIFNRs ( n = 10, 5 females) mice. For (B and E), Benjamini-Hochberg adjusted p value ( q value) are indicated. For (B, E, and G), individual data are presented with a bar at the median.

    Article Snippet: Fixed liver single cell suspensions were hybridized with the Next GEM Single Cell Fixed RNA Mouse Transcriptome Probe Kit (10X Genomics), according to manufacturer instructions, and loaded into a Chromium X (10X Genomics) microfluidics instrument to generate an oil emulsion with partitioned nanoliter-scale droplets, each ideally containing a barcoded gel bead and a single cell, along with enzyme Master Mix (10X Genomics) for probe pair ligation and gel bead primer barcode extension.

    Techniques: Expressing, Staining, MANN-WHITNEY, Clinical Proteomics

    (A) Volcano plots summarizing the results of transcriptome analysis of livers from Dp16 versus wild-type mice fed a low-fat diet (LFD) and from Dp16 mice versus wild-type fed a high-fat diet (HFD) (wild-type LFD n = 10, 4 females, Dp16 LFD n = 8, 4 females, wild-type HFD n = 14, 4 females, Dp16 HFD n = 13, 4 females). Points in blue are in the MMU16 region triplicated in Dp16 mice. (B) Venn diagrams displaying the overlap in the significant differentially expressed genes in the Dp16 triplicated region between HFD fed mice and LFD mice (top) or in the differentially expressed genes that are not triplicated in Dp16 mice (bottom). (C) Scatterplot comparing GSEA NES values for signatures in the livers of Dp16 versus wild-type mice on LFD ( x axis) and Dp16 versus wild-type mice on HFD diet ( y axis). (D) Scatterplots comparing the fold changes of leading-edge genes from the cholesterol homeostasis, fatty acid metabolism, and adipogenesis hallmark gene sets for Dp16 versus wild-type mice on LFD ( x axis) and Dp16 versus wild-type on HFD ( y axis). (E) Sina plots displaying the log 2 (RPKM) of various genes. Horizontal bars indicate median values. Benjamini-Hochberg adjusted p -values ( q values) are indicated. For (C–E), points are colored according to significant in both groups (red), significant in the LFD group only (green), significant in the HFD group only (yellow), or not significant in any group (gray). Significance is defined as q < 0.1 using GSEA or DESeq2.

    Journal: Cell reports

    Article Title: Altered hepatic metabolism in Down syndrome

    doi: 10.1016/j.celrep.2025.116835

    Figure Lengend Snippet: (A) Volcano plots summarizing the results of transcriptome analysis of livers from Dp16 versus wild-type mice fed a low-fat diet (LFD) and from Dp16 mice versus wild-type fed a high-fat diet (HFD) (wild-type LFD n = 10, 4 females, Dp16 LFD n = 8, 4 females, wild-type HFD n = 14, 4 females, Dp16 HFD n = 13, 4 females). Points in blue are in the MMU16 region triplicated in Dp16 mice. (B) Venn diagrams displaying the overlap in the significant differentially expressed genes in the Dp16 triplicated region between HFD fed mice and LFD mice (top) or in the differentially expressed genes that are not triplicated in Dp16 mice (bottom). (C) Scatterplot comparing GSEA NES values for signatures in the livers of Dp16 versus wild-type mice on LFD ( x axis) and Dp16 versus wild-type mice on HFD diet ( y axis). (D) Scatterplots comparing the fold changes of leading-edge genes from the cholesterol homeostasis, fatty acid metabolism, and adipogenesis hallmark gene sets for Dp16 versus wild-type mice on LFD ( x axis) and Dp16 versus wild-type on HFD ( y axis). (E) Sina plots displaying the log 2 (RPKM) of various genes. Horizontal bars indicate median values. Benjamini-Hochberg adjusted p -values ( q values) are indicated. For (C–E), points are colored according to significant in both groups (red), significant in the LFD group only (green), significant in the HFD group only (yellow), or not significant in any group (gray). Significance is defined as q < 0.1 using GSEA or DESeq2.

    Article Snippet: Fixed liver single cell suspensions were hybridized with the Next GEM Single Cell Fixed RNA Mouse Transcriptome Probe Kit (10X Genomics), according to manufacturer instructions, and loaded into a Chromium X (10X Genomics) microfluidics instrument to generate an oil emulsion with partitioned nanoliter-scale droplets, each ideally containing a barcoded gel bead and a single cell, along with enzyme Master Mix (10X Genomics) for probe pair ligation and gel bead primer barcode extension.

    Techniques: