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rabbit anti zo 1 tjp1 antibody  (Bioss)


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    Bioss rabbit anti zo 1 tjp1 antibody
    Rabbit Anti Zo 1 Tjp1 Antibody, supplied by Bioss, used in various techniques. Bioz Stars score: 95/100, based on 109 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+zo+1+tjp1+antibody/ZO-1+Polyclonal+Antibody/10__1016_slash_j__fbio__2025__107512-66-18-43
    Average 95 stars, based on 109 article reviews
    rabbit anti zo 1 tjp1 antibody - by Bioz Stars, 2026-09
    95/100 stars

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    Related Articles

    Western Blot:

    Article Title: Naked Mole-rat-Derived High Molecular Weight Hyaluronic Acid Protects Against DSS-Induced Intestinal Inflammation
    Article Snippet: High-molecular-weight hyaluronic acid (HMW-HA) exerts regulatory effects on intestinal inflammation and tissue repair.. The protective role of CHO-HA (HMW-HA was produced by Chinese hamster ovary (CHO) cell system of cloned naked mole rat HAS2 gene.) against intestinal injury induced by 2 % Dextran Sulfate Sodium Salt (DSS) was validated through methods like: immunohistochemical staining, immunofluorescence staining, Alcian blue staining, hematoxylin and eosin (H&E) staining, Western blotting, ELISA, transepithelial electrical resistance (TEER) measurements, and fluorescein isothiocyanate (FITC)-dextran permeability assays.. CHO-HA may form a physical barrier in the intestinal lumen by upregulating the expression of barrier-associated proteins, thereby mitigating intestinal damage.

    Immunohistochemistry:

    Article Title: Naked Mole-rat-Derived High Molecular Weight Hyaluronic Acid Protects Against DSS-Induced Intestinal Inflammation
    Article Snippet: High-molecular-weight hyaluronic acid (HMW-HA) exerts regulatory effects on intestinal inflammation and tissue repair.. The protective role of CHO-HA (HMW-HA was produced by Chinese hamster ovary (CHO) cell system of cloned naked mole rat HAS2 gene.) against intestinal injury induced by 2 % Dextran Sulfate Sodium Salt (DSS) was validated through methods like: immunohistochemical staining, immunofluorescence staining, Alcian blue staining, hematoxylin and eosin (H&E) staining, Western blotting, ELISA, transepithelial electrical resistance (TEER) measurements, and fluorescein isothiocyanate (FITC)-dextran permeability assays.. CHO-HA may form a physical barrier in the intestinal lumen by upregulating the expression of barrier-associated proteins, thereby mitigating intestinal damage.



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    Warm acupuncture enhances intestinal barrier integrity and suppresses histidine metabolism in CUMS rats. ( A – C ) mRNA expression levels of tight junction–related genes Occludin, <t>Tjp1</t> (ZO-1), and Claudin4 in colonic tissues, determined by RT-qPCR. ( D ) Representative Western blot and quantitative analysis of Occludin, Tjp1, and Claudin4 protein expression in the colon. ( E ) mRNA expression of histidine metabolism–related enzymes HAL and HDC, showing upregulation in CUMS rats and suppression by MMWA intervention. Data are presented as mean ± SD (n = 3–6/group). * p < 0.05, *** p < 0.001 vs Control; # p < 0.05, ## p < 0.01, ### p < 0.001 vs CUMS.
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    Warm acupuncture enhances intestinal barrier integrity and suppresses histidine metabolism in CUMS rats. ( A – C ) mRNA expression levels of tight junction–related genes Occludin, <t>Tjp1</t> (ZO-1), and Claudin4 in colonic tissues, determined by RT-qPCR. ( D ) Representative Western blot and quantitative analysis of Occludin, Tjp1, and Claudin4 protein expression in the colon. ( E ) mRNA expression of histidine metabolism–related enzymes HAL and HDC, showing upregulation in CUMS rats and suppression by MMWA intervention. Data are presented as mean ± SD (n = 3–6/group). * p < 0.05, *** p < 0.001 vs Control; # p < 0.05, ## p < 0.01, ### p < 0.001 vs CUMS.
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    Warm acupuncture enhances intestinal barrier integrity and suppresses histidine metabolism in CUMS rats. ( A – C ) mRNA expression levels of tight junction–related genes Occludin, <t>Tjp1</t> (ZO-1), and Claudin4 in colonic tissues, determined by RT-qPCR. ( D ) Representative Western blot and quantitative analysis of Occludin, Tjp1, and Claudin4 protein expression in the colon. ( E ) mRNA expression of histidine metabolism–related enzymes HAL and HDC, showing upregulation in CUMS rats and suppression by MMWA intervention. Data are presented as mean ± SD (n = 3–6/group). * p < 0.05, *** p < 0.001 vs Control; # p < 0.05, ## p < 0.01, ### p < 0.001 vs CUMS.
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    Image Search Results


    Warm acupuncture enhances intestinal barrier integrity and suppresses histidine metabolism in CUMS rats. ( A – C ) mRNA expression levels of tight junction–related genes Occludin, Tjp1 (ZO-1), and Claudin4 in colonic tissues, determined by RT-qPCR. ( D ) Representative Western blot and quantitative analysis of Occludin, Tjp1, and Claudin4 protein expression in the colon. ( E ) mRNA expression of histidine metabolism–related enzymes HAL and HDC, showing upregulation in CUMS rats and suppression by MMWA intervention. Data are presented as mean ± SD (n = 3–6/group). * p < 0.05, *** p < 0.001 vs Control; # p < 0.05, ## p < 0.01, ### p < 0.001 vs CUMS.

    Journal: Neuropsychiatric Disease and Treatment

    Article Title: Antidepressant-Like Effects of Mongolian Medical Warm Acupuncture via Remodeling the Gut Microbiota–Metabolite–Barrier Axis in CUMS Rats

    doi: 10.2147/NDT.S566386

    Figure Lengend Snippet: Warm acupuncture enhances intestinal barrier integrity and suppresses histidine metabolism in CUMS rats. ( A – C ) mRNA expression levels of tight junction–related genes Occludin, Tjp1 (ZO-1), and Claudin4 in colonic tissues, determined by RT-qPCR. ( D ) Representative Western blot and quantitative analysis of Occludin, Tjp1, and Claudin4 protein expression in the colon. ( E ) mRNA expression of histidine metabolism–related enzymes HAL and HDC, showing upregulation in CUMS rats and suppression by MMWA intervention. Data are presented as mean ± SD (n = 3–6/group). * p < 0.05, *** p < 0.001 vs Control; # p < 0.05, ## p < 0.01, ### p < 0.001 vs CUMS.

    Article Snippet: Membranes were blocked and incubated overnight at 4 °C with primary antibodies against Occludin (1:1000, Abcam, ab216327), TJP1 (ZO-1, 1:1000, CST, # 13663), Claudin4 (1:1000, Abcam, ab15104), HAL (1:500, Proteintech, 15756-1-AP), HDC (1:500, Santa Cruz, sc-271213), and β-actin (1:2000, Abcam, ab8226).

    Techniques: Expressing, Quantitative RT-PCR, Western Blot, Control