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gfap  (Proteintech)


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    Proteintech gfap
    PDA-HP/NIR treatment suppresses glial activation and promotes a shift toward anti-inflammatory polarization following SCI. (A) Representative fluorescence images and quantification showing <t>GFAP</t> (green) and IBA1 (red) staining of spinal cord sections in each group. Scale bars are 10 μm. Quantification of mean fluorescence intensity is shown in (B, C). Data are presented as mean ± SD ( n = 6, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001). (D) Representative fluorescence images and quantification showing Arg-1 (green) and iNOS (red) staining of spinal cord sections in each group. Scale bars are 10 μm. Quantification of mean fluorescence intensity is shown in (E, F). Data are presented as mean ± SD ( n = 6, ∗ p = 0.011, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
    Gfap, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 587 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/60190+1+ig/pmc12856442-126-13-17?v=Proteintech
    Average 96 stars, based on 587 article reviews
    gfap - by Bioz Stars, 2026-07
    96/100 stars

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    1) Product Images from "Dual-responsive PDA-HP hydrogel enables mitochondria-targeted mild photothermal therapy for spinal cord repair"

    Article Title: Dual-responsive PDA-HP hydrogel enables mitochondria-targeted mild photothermal therapy for spinal cord repair

    Journal: Materials Today Bio

    doi: 10.1016/j.mtbio.2026.102783

    PDA-HP/NIR treatment suppresses glial activation and promotes a shift toward anti-inflammatory polarization following SCI. (A) Representative fluorescence images and quantification showing GFAP (green) and IBA1 (red) staining of spinal cord sections in each group. Scale bars are 10 μm. Quantification of mean fluorescence intensity is shown in (B, C). Data are presented as mean ± SD ( n = 6, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001). (D) Representative fluorescence images and quantification showing Arg-1 (green) and iNOS (red) staining of spinal cord sections in each group. Scale bars are 10 μm. Quantification of mean fluorescence intensity is shown in (E, F). Data are presented as mean ± SD ( n = 6, ∗ p = 0.011, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
    Figure Legend Snippet: PDA-HP/NIR treatment suppresses glial activation and promotes a shift toward anti-inflammatory polarization following SCI. (A) Representative fluorescence images and quantification showing GFAP (green) and IBA1 (red) staining of spinal cord sections in each group. Scale bars are 10 μm. Quantification of mean fluorescence intensity is shown in (B, C). Data are presented as mean ± SD ( n = 6, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001). (D) Representative fluorescence images and quantification showing Arg-1 (green) and iNOS (red) staining of spinal cord sections in each group. Scale bars are 10 μm. Quantification of mean fluorescence intensity is shown in (E, F). Data are presented as mean ± SD ( n = 6, ∗ p = 0.011, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Techniques Used: Activation Assay, Fluorescence, Staining



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    PDA-HP/NIR treatment suppresses glial activation and promotes a shift toward anti-inflammatory polarization following SCI. (A) Representative fluorescence images and quantification showing <t>GFAP</t> (green) and IBA1 (red) staining of spinal cord sections in each group. Scale bars are 10 μm. Quantification of mean fluorescence intensity is shown in (B, C). Data are presented as mean ± SD ( n = 6, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001). (D) Representative fluorescence images and quantification showing Arg-1 (green) and iNOS (red) staining of spinal cord sections in each group. Scale bars are 10 μm. Quantification of mean fluorescence intensity is shown in (E, F). Data are presented as mean ± SD ( n = 6, ∗ p = 0.011, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
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    PDA-HP/NIR treatment suppresses glial activation and promotes a shift toward anti-inflammatory polarization following SCI. (A) Representative fluorescence images and quantification showing <t>GFAP</t> (green) and IBA1 (red) staining of spinal cord sections in each group. Scale bars are 10 μm. Quantification of mean fluorescence intensity is shown in (B, C). Data are presented as mean ± SD ( n = 6, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001). (D) Representative fluorescence images and quantification showing Arg-1 (green) and iNOS (red) staining of spinal cord sections in each group. Scale bars are 10 μm. Quantification of mean fluorescence intensity is shown in (E, F). Data are presented as mean ± SD ( n = 6, ∗ p = 0.011, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
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    PDA-HP/NIR treatment suppresses glial activation and promotes a shift toward anti-inflammatory polarization following SCI. (A) Representative fluorescence images and quantification showing <t>GFAP</t> (green) and IBA1 (red) staining of spinal cord sections in each group. Scale bars are 10 μm. Quantification of mean fluorescence intensity is shown in (B, C). Data are presented as mean ± SD ( n = 6, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001). (D) Representative fluorescence images and quantification showing Arg-1 (green) and iNOS (red) staining of spinal cord sections in each group. Scale bars are 10 μm. Quantification of mean fluorescence intensity is shown in (E, F). Data are presented as mean ± SD ( n = 6, ∗ p = 0.011, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
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    Image Search Results


    PDA-HP/NIR treatment suppresses glial activation and promotes a shift toward anti-inflammatory polarization following SCI. (A) Representative fluorescence images and quantification showing GFAP (green) and IBA1 (red) staining of spinal cord sections in each group. Scale bars are 10 μm. Quantification of mean fluorescence intensity is shown in (B, C). Data are presented as mean ± SD ( n = 6, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001). (D) Representative fluorescence images and quantification showing Arg-1 (green) and iNOS (red) staining of spinal cord sections in each group. Scale bars are 10 μm. Quantification of mean fluorescence intensity is shown in (E, F). Data are presented as mean ± SD ( n = 6, ∗ p = 0.011, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Journal: Materials Today Bio

    Article Title: Dual-responsive PDA-HP hydrogel enables mitochondria-targeted mild photothermal therapy for spinal cord repair

    doi: 10.1016/j.mtbio.2026.102783

    Figure Lengend Snippet: PDA-HP/NIR treatment suppresses glial activation and promotes a shift toward anti-inflammatory polarization following SCI. (A) Representative fluorescence images and quantification showing GFAP (green) and IBA1 (red) staining of spinal cord sections in each group. Scale bars are 10 μm. Quantification of mean fluorescence intensity is shown in (B, C). Data are presented as mean ± SD ( n = 6, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001). (D) Representative fluorescence images and quantification showing Arg-1 (green) and iNOS (red) staining of spinal cord sections in each group. Scale bars are 10 μm. Quantification of mean fluorescence intensity is shown in (E, F). Data are presented as mean ± SD ( n = 6, ∗ p = 0.011, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Article Snippet: Samples were then incubated overnight at 4 °C with the following primary antibodies: GFAP (astrocyte marker, 1:500, Proteintech, China), Iba1 (microglia marker, 1:500, Proteintech, China), Arg-1 (M2 phenotype marker, 1:500, Proteintech, China), iNOS (M1 phenotype marker, 1:500, Proteintech, China).

    Techniques: Activation Assay, Fluorescence, Staining