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antibodies s100β 1  (Bioss)


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    Structured Review

    Bioss antibodies s100β 1
    Antibodies S100β 1, supplied by Bioss, used in various techniques. Bioz Stars score: 94/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/antibodies s100β 1/product/Bioss
    Average 94 stars, based on 7 article reviews
    antibodies s100β 1 - by Bioz Stars, 2026-02
    94/100 stars

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    s100  (Bioss)
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    Effect of TMAO on the proliferation and expression of AQP4, GFAP, and <t>S100</t> in astrocytes. (A–C) Immunofluorescence detection of changes in the fluorescence intensity of AQP4, GFAP, and S100. (D) TUNEL assay detection of cell apoptosis. N = 3 for each group, analysis of variance followed by LSD or Dunnett's post-hoc test was used to compare between-group differences. 'ns' indicates that there was no significant difference between the groups.
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    Effect of TMAO on the proliferation and expression of AQP4, GFAP, and <t>S100</t> in astrocytes. (A–C) Immunofluorescence detection of changes in the fluorescence intensity of AQP4, GFAP, and S100. (D) TUNEL assay detection of cell apoptosis. N = 3 for each group, analysis of variance followed by LSD or Dunnett's post-hoc test was used to compare between-group differences. 'ns' indicates that there was no significant difference between the groups.
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    Effect of TMAO on the proliferation and expression of AQP4, GFAP, and <t>S100</t> in astrocytes. (A–C) Immunofluorescence detection of changes in the fluorescence intensity of AQP4, GFAP, and S100. (D) TUNEL assay detection of cell apoptosis. N = 3 for each group, analysis of variance followed by LSD or Dunnett's post-hoc test was used to compare between-group differences. 'ns' indicates that there was no significant difference between the groups.
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    Bioss primary antibodies
    Effect of TMAO on the proliferation and expression of AQP4, GFAP, and <t>S100</t> in astrocytes. (A–C) Immunofluorescence detection of changes in the fluorescence intensity of AQP4, GFAP, and S100. (D) TUNEL assay detection of cell apoptosis. N = 3 for each group, analysis of variance followed by LSD or Dunnett's post-hoc test was used to compare between-group differences. 'ns' indicates that there was no significant difference between the groups.
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    Effect of TMAO on the proliferation and expression of AQP4, GFAP, and <t>S100</t> in astrocytes. (A–C) Immunofluorescence detection of changes in the fluorescence intensity of AQP4, GFAP, and S100. (D) TUNEL assay detection of cell apoptosis. N = 3 for each group, analysis of variance followed by LSD or Dunnett's post-hoc test was used to compare between-group differences. 'ns' indicates that there was no significant difference between the groups.
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    Image Search Results


    Effect of TMAO on the proliferation and expression of AQP4, GFAP, and S100 in astrocytes. (A–C) Immunofluorescence detection of changes in the fluorescence intensity of AQP4, GFAP, and S100. (D) TUNEL assay detection of cell apoptosis. N = 3 for each group, analysis of variance followed by LSD or Dunnett's post-hoc test was used to compare between-group differences. 'ns' indicates that there was no significant difference between the groups.

    Journal: IBRO Neuroscience Reports

    Article Title: Trimethylamine-N-oxide damages astrocytes and lymphatic endothelial cells in the cerebral lymphatic system

    doi: 10.1016/j.ibneur.2025.09.001

    Figure Lengend Snippet: Effect of TMAO on the proliferation and expression of AQP4, GFAP, and S100 in astrocytes. (A–C) Immunofluorescence detection of changes in the fluorescence intensity of AQP4, GFAP, and S100. (D) TUNEL assay detection of cell apoptosis. N = 3 for each group, analysis of variance followed by LSD or Dunnett's post-hoc test was used to compare between-group differences. 'ns' indicates that there was no significant difference between the groups.

    Article Snippet: The primary antibodies used include S100 (1: 100, bs-1248R, Bioss, China), glial fibrillary acidic protein (GFAP, 1: 100, R380620, Zenbio, China), AQP4 (1: 200, A11210, ABclonal, China), claudin-5 (1: 200, A10207 , ABclonal, China), and Ocln (1: 200, YN2865, Immunoway, China), and the secondary antibody was goat anti-rabbit IgG (1: 500, 550076, Zenbio, China).

    Techniques: Expressing, Immunofluorescence, Fluorescence, TUNEL Assay

    Effects of TMAO on intracranial inflammation and functional proteins in animals. Levels of IL-6, NLRP3, TNF-α, and SNCA in the cerebrospinal fluid detected by ELISA. (B) The injury of ventral midbrain neurons detected by Nissl staining. (C) Immunofluorescence was used to detect the effects of TMAO on AQP4, GFAP, S100, claudin-5, and Ocln in the ventral midbrain of mice. Three animals were randomly selected from each group (n = 10) for sample testing, analysis of variance followed by LSD or Dunnett's post-hoc test was used to compare between-group differences. 'ns' indicates that there was no significant difference between the groups.

    Journal: IBRO Neuroscience Reports

    Article Title: Trimethylamine-N-oxide damages astrocytes and lymphatic endothelial cells in the cerebral lymphatic system

    doi: 10.1016/j.ibneur.2025.09.001

    Figure Lengend Snippet: Effects of TMAO on intracranial inflammation and functional proteins in animals. Levels of IL-6, NLRP3, TNF-α, and SNCA in the cerebrospinal fluid detected by ELISA. (B) The injury of ventral midbrain neurons detected by Nissl staining. (C) Immunofluorescence was used to detect the effects of TMAO on AQP4, GFAP, S100, claudin-5, and Ocln in the ventral midbrain of mice. Three animals were randomly selected from each group (n = 10) for sample testing, analysis of variance followed by LSD or Dunnett's post-hoc test was used to compare between-group differences. 'ns' indicates that there was no significant difference between the groups.

    Article Snippet: The primary antibodies used include S100 (1: 100, bs-1248R, Bioss, China), glial fibrillary acidic protein (GFAP, 1: 100, R380620, Zenbio, China), AQP4 (1: 200, A11210, ABclonal, China), claudin-5 (1: 200, A10207 , ABclonal, China), and Ocln (1: 200, YN2865, Immunoway, China), and the secondary antibody was goat anti-rabbit IgG (1: 500, 550076, Zenbio, China).

    Techniques: Functional Assay, Enzyme-linked Immunosorbent Assay, Staining, Immunofluorescence