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sall1 antibody  (Thermo Fisher)


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    Thermo Fisher sall1 antibody
    ZIKV results in activated microglia with a change in morphology. (A) CX3CR1-GFP mice were injected with ZIKV at 10^6 PFU via footpad, brains were harvested at 0 and 7dpi. (B) 100X immunofluorescence imaging of mouse cortex staining for DAPI and CX3CR1. (C) 100X immunofluorescence of mouse cortex to assess microglial morphology using <t>sall1</t> and CX3CR1-GFP. (D) PCR data for CD86, CX3CR1 and CH25H genes, N=3. Data represents the mean ± SD ∗ p < 0.0332, ∗∗ p < 0.0021. The experiment was independently repeated twice with similar results; representative data are shown.
    Sall1 Antibody, supplied by Thermo Fisher, 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/result/sall1 antibody/product/Thermo Fisher
    Average 90 stars, based on 1 article reviews
    sall1 antibody - by Bioz Stars, 2026-03
    90/100 stars

    Images

    1) Product Images from "Zika virus induces monocyte recruitment in the immunocompetent adult brain driving chronic inflammation"

    Article Title: Zika virus induces monocyte recruitment in the immunocompetent adult brain driving chronic inflammation

    Journal: Frontiers in Immunology

    doi: 10.3389/fimmu.2025.1597776

    ZIKV results in activated microglia with a change in morphology. (A) CX3CR1-GFP mice were injected with ZIKV at 10^6 PFU via footpad, brains were harvested at 0 and 7dpi. (B) 100X immunofluorescence imaging of mouse cortex staining for DAPI and CX3CR1. (C) 100X immunofluorescence of mouse cortex to assess microglial morphology using sall1 and CX3CR1-GFP. (D) PCR data for CD86, CX3CR1 and CH25H genes, N=3. Data represents the mean ± SD ∗ p < 0.0332, ∗∗ p < 0.0021. The experiment was independently repeated twice with similar results; representative data are shown.
    Figure Legend Snippet: ZIKV results in activated microglia with a change in morphology. (A) CX3CR1-GFP mice were injected with ZIKV at 10^6 PFU via footpad, brains were harvested at 0 and 7dpi. (B) 100X immunofluorescence imaging of mouse cortex staining for DAPI and CX3CR1. (C) 100X immunofluorescence of mouse cortex to assess microglial morphology using sall1 and CX3CR1-GFP. (D) PCR data for CD86, CX3CR1 and CH25H genes, N=3. Data represents the mean ± SD ∗ p < 0.0332, ∗∗ p < 0.0021. The experiment was independently repeated twice with similar results; representative data are shown.

    Techniques Used: Injection, Immunofluorescence, Imaging, Staining

    Infiltrating monocytes seen in ZIKV mice brains at 7dpi. (A) CCR2-CreER;R26R-EGFP (Ai6) mice were given tamoxifen for 3 days before infected with ZIKV and harvested. (B) Quantification of flow data for Bone marrow cells (CCR2-EGFP+, CCR2-EGFP+ CD68+) (C) Quantification of flow data for Brain cells (CD11B+CD45+, CD45int CD11B+ (Microglia), CCR2-EGFP+, CCR2-EGFP-). (D, E) Immunofluorescence of CCR2-CreER-R26R-EGFP mice for EGFP and sall1 expression in choroid plexus region with quantification. N=3-4. Data represents the mean ± SD ∗ p < 0.0332, ∗∗ p < 0.0021, and ∗∗∗ p < 0.0002.
    Figure Legend Snippet: Infiltrating monocytes seen in ZIKV mice brains at 7dpi. (A) CCR2-CreER;R26R-EGFP (Ai6) mice were given tamoxifen for 3 days before infected with ZIKV and harvested. (B) Quantification of flow data for Bone marrow cells (CCR2-EGFP+, CCR2-EGFP+ CD68+) (C) Quantification of flow data for Brain cells (CD11B+CD45+, CD45int CD11B+ (Microglia), CCR2-EGFP+, CCR2-EGFP-). (D, E) Immunofluorescence of CCR2-CreER-R26R-EGFP mice for EGFP and sall1 expression in choroid plexus region with quantification. N=3-4. Data represents the mean ± SD ∗ p < 0.0332, ∗∗ p < 0.0021, and ∗∗∗ p < 0.0002.

    Techniques Used: Infection, Immunofluorescence, Expressing



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    Image Search Results


    ZIKV results in activated microglia with a change in morphology. (A) CX3CR1-GFP mice were injected with ZIKV at 10^6 PFU via footpad, brains were harvested at 0 and 7dpi. (B) 100X immunofluorescence imaging of mouse cortex staining for DAPI and CX3CR1. (C) 100X immunofluorescence of mouse cortex to assess microglial morphology using sall1 and CX3CR1-GFP. (D) PCR data for CD86, CX3CR1 and CH25H genes, N=3. Data represents the mean ± SD ∗ p < 0.0332, ∗∗ p < 0.0021. The experiment was independently repeated twice with similar results; representative data are shown.

    Journal: Frontiers in Immunology

    Article Title: Zika virus induces monocyte recruitment in the immunocompetent adult brain driving chronic inflammation

    doi: 10.3389/fimmu.2025.1597776

    Figure Lengend Snippet: ZIKV results in activated microglia with a change in morphology. (A) CX3CR1-GFP mice were injected with ZIKV at 10^6 PFU via footpad, brains were harvested at 0 and 7dpi. (B) 100X immunofluorescence imaging of mouse cortex staining for DAPI and CX3CR1. (C) 100X immunofluorescence of mouse cortex to assess microglial morphology using sall1 and CX3CR1-GFP. (D) PCR data for CD86, CX3CR1 and CH25H genes, N=3. Data represents the mean ± SD ∗ p < 0.0332, ∗∗ p < 0.0021. The experiment was independently repeated twice with similar results; representative data are shown.

    Article Snippet: Primary antibodies used were SALL1 (eBioscience), and GFAP (sc33673), and secondary antibodies used were AF647 (Invitrogen).

    Techniques: Injection, Immunofluorescence, Imaging, Staining

    Infiltrating monocytes seen in ZIKV mice brains at 7dpi. (A) CCR2-CreER;R26R-EGFP (Ai6) mice were given tamoxifen for 3 days before infected with ZIKV and harvested. (B) Quantification of flow data for Bone marrow cells (CCR2-EGFP+, CCR2-EGFP+ CD68+) (C) Quantification of flow data for Brain cells (CD11B+CD45+, CD45int CD11B+ (Microglia), CCR2-EGFP+, CCR2-EGFP-). (D, E) Immunofluorescence of CCR2-CreER-R26R-EGFP mice for EGFP and sall1 expression in choroid plexus region with quantification. N=3-4. Data represents the mean ± SD ∗ p < 0.0332, ∗∗ p < 0.0021, and ∗∗∗ p < 0.0002.

    Journal: Frontiers in Immunology

    Article Title: Zika virus induces monocyte recruitment in the immunocompetent adult brain driving chronic inflammation

    doi: 10.3389/fimmu.2025.1597776

    Figure Lengend Snippet: Infiltrating monocytes seen in ZIKV mice brains at 7dpi. (A) CCR2-CreER;R26R-EGFP (Ai6) mice were given tamoxifen for 3 days before infected with ZIKV and harvested. (B) Quantification of flow data for Bone marrow cells (CCR2-EGFP+, CCR2-EGFP+ CD68+) (C) Quantification of flow data for Brain cells (CD11B+CD45+, CD45int CD11B+ (Microglia), CCR2-EGFP+, CCR2-EGFP-). (D, E) Immunofluorescence of CCR2-CreER-R26R-EGFP mice for EGFP and sall1 expression in choroid plexus region with quantification. N=3-4. Data represents the mean ± SD ∗ p < 0.0332, ∗∗ p < 0.0021, and ∗∗∗ p < 0.0002.

    Article Snippet: Primary antibodies used were SALL1 (eBioscience), and GFAP (sc33673), and secondary antibodies used were AF647 (Invitrogen).

    Techniques: Infection, Immunofluorescence, Expressing