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gfap pe  (Miltenyi Biotec)


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    Miltenyi Biotec gfap pe
    Gfap Pe, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 94/100, based on 15 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/gfap pe/product/Miltenyi Biotec
    Average 94 stars, based on 15 article reviews
    gfap pe - by Bioz Stars, 2026-02
    94/100 stars

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    ( a & b ) Example of immunohistological sample of Iso clone, 42 days post transduction with AAV6 and labeled with either (a) <t>GFP,</t> <t>MAP2,</t> and DAPI or (b) GFP, <t>GFAP,</t> and DAPI. Dotted square indicates enlarged area. White arrows indicate co-staining of GFP with either (b) MAP2 or (b) GFAP. All hCOs were harvested on day 120, 10 days post AAV transduction. ( c ) Flow cytometry quantification of % GFP labeled cells for each AAV serotype in each hCO clone. ( d ) Flow cytometry quantification of % GFP and MAP2 co-labeled cells for each AAV serotype in each hCO clone. ( e ) Flow cytometry quantification % GFP and GFAP co-labeled cells for each AAV serotype in each hCO clone. All hCOs were harvested on day 120, 10 days post AAV transduction. ( n = 4 hCOs per condition, statistical significance between AAV6 and AAV2 or AAV9 serotypes determined by one-way ANOVA with Tukey post-hoc tests, *** p < 0.001, ** p < 0.01. Values for comparisons between other serotypes are in Supplementary Tables 1-9).
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    Image Search Results


    Immunophenotyping panel for multiplexed tissue imaging of cancer.

    Journal: Frontiers in Immunology

    Article Title: Unveiling spatial complexity in solid tumor immune microenvironments through multiplexed imaging

    doi: 10.3389/fimmu.2024.1383932

    Figure Lengend Snippet: Immunophenotyping panel for multiplexed tissue imaging of cancer.

    Article Snippet: GFAP , REA335 , 50 , 130-118-351 , PE , Miltenyi Biotec.

    Techniques: Imaging

    ( a & b ) Example of immunohistological sample of Iso clone, 42 days post transduction with AAV6 and labeled with either (a) GFP, MAP2, and DAPI or (b) GFP, GFAP, and DAPI. Dotted square indicates enlarged area. White arrows indicate co-staining of GFP with either (b) MAP2 or (b) GFAP. All hCOs were harvested on day 120, 10 days post AAV transduction. ( c ) Flow cytometry quantification of % GFP labeled cells for each AAV serotype in each hCO clone. ( d ) Flow cytometry quantification of % GFP and MAP2 co-labeled cells for each AAV serotype in each hCO clone. ( e ) Flow cytometry quantification % GFP and GFAP co-labeled cells for each AAV serotype in each hCO clone. All hCOs were harvested on day 120, 10 days post AAV transduction. ( n = 4 hCOs per condition, statistical significance between AAV6 and AAV2 or AAV9 serotypes determined by one-way ANOVA with Tukey post-hoc tests, *** p < 0.001, ** p < 0.01. Values for comparisons between other serotypes are in Supplementary Tables 1-9).

    Journal: bioRxiv

    Article Title: Cell specificity of adeno-associated virus (AAV) serotypes in human cortical organoids

    doi: 10.1101/2023.04.13.536491

    Figure Lengend Snippet: ( a & b ) Example of immunohistological sample of Iso clone, 42 days post transduction with AAV6 and labeled with either (a) GFP, MAP2, and DAPI or (b) GFP, GFAP, and DAPI. Dotted square indicates enlarged area. White arrows indicate co-staining of GFP with either (b) MAP2 or (b) GFAP. All hCOs were harvested on day 120, 10 days post AAV transduction. ( c ) Flow cytometry quantification of % GFP labeled cells for each AAV serotype in each hCO clone. ( d ) Flow cytometry quantification of % GFP and MAP2 co-labeled cells for each AAV serotype in each hCO clone. ( e ) Flow cytometry quantification % GFP and GFAP co-labeled cells for each AAV serotype in each hCO clone. All hCOs were harvested on day 120, 10 days post AAV transduction. ( n = 4 hCOs per condition, statistical significance between AAV6 and AAV2 or AAV9 serotypes determined by one-way ANOVA with Tukey post-hoc tests, *** p < 0.001, ** p < 0.01. Values for comparisons between other serotypes are in Supplementary Tables 1-9).

    Article Snippet: Cells were centrifuged at 1000 rpm and resuspended in flow buffer containing the primary antibodies: rat GFP (Biolegend, 338001, 1:200), guinea pig MAP2 (Synaptic Systems, 188004, 1:4000), and or mouse GFAP-PE (Miltenyi Biotech, 130-118-351, 1:50).

    Techniques: Transduction, Labeling, Staining, Flow Cytometry