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electron microscopy research service  (China Pharmaceuticals Inc)

 
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    China Pharmaceuticals Inc electron microscopy research service
    Arginine inhibits S. Typhimurium infection by interacting with RPS3 (-B) Enrichment analysis of RAW264.7 cells cell lysate and arginine binding protein , pathway (A) and heatmap of protein abundance associated with Salmonella infection ( B, C ) Knockdown efficiency of RPS3 in RAW264.7 cell line was verified by Western blotting ( n = 5 independent experiments). (D) DCFH-DA fluorescent probe assay for detection of cellular ROS Levels ( n = 5 independent experiments). (E) Representative confocal <t>microscopy</t> image illustrating the mitochondrial abundance within macrophages ( n = 5 independent experiments). (F) Venn diagram of RPS3 binding, arginine metabolism, and protein overlap associated with Salmonella infection. (G) Interactions between RPS3 interaction with SRSF3 was analyzed using the GeneMANIA database. (H) RPS3 and SRSF3 by co-immunoprecipitation assays using anti-SRSF3 antibodies. The data are reported as the mean ± SD. **p < 0.01.
    Electron Microscopy Research Service, supplied by China Pharmaceuticals 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/result/electron microscopy research service/product/China Pharmaceuticals Inc
    Average 86 stars, based on 1 article reviews
    electron microscopy research service - by Bioz Stars, 2026-06
    86/100 stars

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    1) Product Images from "Arginine-mediated inhibition of macrophage apoptosis by Escherichia coli nissle 1917 in Salmonella typhimurium-induced intestinal inflammation"

    Article Title: Arginine-mediated inhibition of macrophage apoptosis by Escherichia coli nissle 1917 in Salmonella typhimurium-induced intestinal inflammation

    Journal: Frontiers in Immunology

    doi: 10.3389/fimmu.2025.1684234

    Arginine inhibits S. Typhimurium infection by interacting with RPS3 (-B) Enrichment analysis of RAW264.7 cells cell lysate and arginine binding protein , pathway (A) and heatmap of protein abundance associated with Salmonella infection ( B, C ) Knockdown efficiency of RPS3 in RAW264.7 cell line was verified by Western blotting ( n = 5 independent experiments). (D) DCFH-DA fluorescent probe assay for detection of cellular ROS Levels ( n = 5 independent experiments). (E) Representative confocal microscopy image illustrating the mitochondrial abundance within macrophages ( n = 5 independent experiments). (F) Venn diagram of RPS3 binding, arginine metabolism, and protein overlap associated with Salmonella infection. (G) Interactions between RPS3 interaction with SRSF3 was analyzed using the GeneMANIA database. (H) RPS3 and SRSF3 by co-immunoprecipitation assays using anti-SRSF3 antibodies. The data are reported as the mean ± SD. **p < 0.01.
    Figure Legend Snippet: Arginine inhibits S. Typhimurium infection by interacting with RPS3 (-B) Enrichment analysis of RAW264.7 cells cell lysate and arginine binding protein , pathway (A) and heatmap of protein abundance associated with Salmonella infection ( B, C ) Knockdown efficiency of RPS3 in RAW264.7 cell line was verified by Western blotting ( n = 5 independent experiments). (D) DCFH-DA fluorescent probe assay for detection of cellular ROS Levels ( n = 5 independent experiments). (E) Representative confocal microscopy image illustrating the mitochondrial abundance within macrophages ( n = 5 independent experiments). (F) Venn diagram of RPS3 binding, arginine metabolism, and protein overlap associated with Salmonella infection. (G) Interactions between RPS3 interaction with SRSF3 was analyzed using the GeneMANIA database. (H) RPS3 and SRSF3 by co-immunoprecipitation assays using anti-SRSF3 antibodies. The data are reported as the mean ± SD. **p < 0.01.

    Techniques Used: Infection, Binding Assay, Quantitative Proteomics, Knockdown, Western Blot, Confocal Microscopy, Immunoprecipitation



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    Arginine inhibits S. Typhimurium infection by interacting with RPS3 (-B) Enrichment analysis of RAW264.7 cells cell lysate and arginine binding protein , pathway (A) and heatmap of protein abundance associated with Salmonella infection ( B, C ) Knockdown efficiency of RPS3 in RAW264.7 cell line was verified by Western blotting ( n = 5 independent experiments). (D) DCFH-DA fluorescent probe assay for detection of cellular ROS Levels ( n = 5 independent experiments). (E) Representative confocal <t>microscopy</t> image illustrating the mitochondrial abundance within macrophages ( n = 5 independent experiments). (F) Venn diagram of RPS3 binding, arginine metabolism, and protein overlap associated with Salmonella infection. (G) Interactions between RPS3 interaction with SRSF3 was analyzed using the GeneMANIA database. (H) RPS3 and SRSF3 by co-immunoprecipitation assays using anti-SRSF3 antibodies. The data are reported as the mean ± SD. **p < 0.01.
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    Arginine inhibits S. Typhimurium infection by interacting with RPS3 (-B) Enrichment analysis of RAW264.7 cells cell lysate and arginine binding protein , pathway (A) and heatmap of protein abundance associated with Salmonella infection ( B, C ) Knockdown efficiency of RPS3 in RAW264.7 cell line was verified by Western blotting ( n = 5 independent experiments). (D) DCFH-DA fluorescent probe assay for detection of cellular ROS Levels ( n = 5 independent experiments). (E) Representative confocal <t>microscopy</t> image illustrating the mitochondrial abundance within macrophages ( n = 5 independent experiments). (F) Venn diagram of RPS3 binding, arginine metabolism, and protein overlap associated with Salmonella infection. (G) Interactions between RPS3 interaction with SRSF3 was analyzed using the GeneMANIA database. (H) RPS3 and SRSF3 by co-immunoprecipitation assays using anti-SRSF3 antibodies. The data are reported as the mean ± SD. **p < 0.01.
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    Arginine inhibits S. Typhimurium infection by interacting with RPS3 (-B) Enrichment analysis of RAW264.7 cells cell lysate and arginine binding protein , pathway (A) and heatmap of protein abundance associated with Salmonella infection ( B, C ) Knockdown efficiency of RPS3 in RAW264.7 cell line was verified by Western blotting ( n = 5 independent experiments). (D) DCFH-DA fluorescent probe assay for detection of cellular ROS Levels ( n = 5 independent experiments). (E) Representative confocal microscopy image illustrating the mitochondrial abundance within macrophages ( n = 5 independent experiments). (F) Venn diagram of RPS3 binding, arginine metabolism, and protein overlap associated with Salmonella infection. (G) Interactions between RPS3 interaction with SRSF3 was analyzed using the GeneMANIA database. (H) RPS3 and SRSF3 by co-immunoprecipitation assays using anti-SRSF3 antibodies. The data are reported as the mean ± SD. **p < 0.01.

    Journal: Frontiers in Immunology

    Article Title: Arginine-mediated inhibition of macrophage apoptosis by Escherichia coli nissle 1917 in Salmonella typhimurium-induced intestinal inflammation

    doi: 10.3389/fimmu.2025.1684234

    Figure Lengend Snippet: Arginine inhibits S. Typhimurium infection by interacting with RPS3 (-B) Enrichment analysis of RAW264.7 cells cell lysate and arginine binding protein , pathway (A) and heatmap of protein abundance associated with Salmonella infection ( B, C ) Knockdown efficiency of RPS3 in RAW264.7 cell line was verified by Western blotting ( n = 5 independent experiments). (D) DCFH-DA fluorescent probe assay for detection of cellular ROS Levels ( n = 5 independent experiments). (E) Representative confocal microscopy image illustrating the mitochondrial abundance within macrophages ( n = 5 independent experiments). (F) Venn diagram of RPS3 binding, arginine metabolism, and protein overlap associated with Salmonella infection. (G) Interactions between RPS3 interaction with SRSF3 was analyzed using the GeneMANIA database. (H) RPS3 and SRSF3 by co-immunoprecipitation assays using anti-SRSF3 antibodies. The data are reported as the mean ± SD. **p < 0.01.

    Article Snippet: Cellular collectives were fixed with 2.5% glutaraldehyde for 24 h, embedded in 2% agarose, and processed by the Electron Microscopy Research Service of China Pharmaceutical University.

    Techniques: Infection, Binding Assay, Quantitative Proteomics, Knockdown, Western Blot, Confocal Microscopy, Immunoprecipitation