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anti-snap23 111202  (Synaptic Systems)


Bioz Manufacturer Symbol Synaptic Systems manufactures this product  
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    Structured Review

    Synaptic Systems anti-snap23 111202
    Anti Snap23 111202, supplied by Synaptic Systems, 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/anti-snap23 111202/product/Synaptic Systems
    Average 90 stars, based on 1 article reviews
    anti-snap23 111202 - by Bioz Stars, 2026-03
    90/100 stars

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    (A) Wide-field fluorescence images of untreated HBE cells (left) and HBE cells with CFTR ΔF508 mutation treated with increasing concentrations of porosomes (0.5, and 1 µg). The scale bar represents 50 µm. DAPI (blue) stains the nuclei, and CFTR (green) highlights the CFTR protein. ( B) Magnify-processed images of the same conditions as in Panel A, showing enhanced resolution and detail of CFTR expression. The scale bar represents 50 µm. ( C) Zoomed-in images of the areas indicated by yellow-dotted boxes in Panel B. These images provide a closer view of CFTR expression in the HBE cells. The scale bar represents 5 µm. (D) Magnify-processed images of CFTR ΔF508-mutated HBE cells treated with increasing doses of porosomes (0.2, 0.5, and 1 µg). This panel shows DAPI (blue), CFTR (green), and <t>SNAP23</t> (red), illustrating the expression and localization of both proteins in response to porosome treatment. The scale bar represents 5 µm in biological scale. B, C and D: The expansion factor is 3.8× (1× PBS).
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    (A) Wide-field fluorescence images of untreated HBE cells (left) and HBE cells with CFTR ΔF508 mutation treated with increasing concentrations of porosomes (0.5, and 1 µg). The scale bar represents 50 µm. DAPI (blue) stains the nuclei, and CFTR (green) highlights the CFTR protein. ( B) Magnify-processed images of the same conditions as in Panel A, showing enhanced resolution and detail of CFTR expression. The scale bar represents 50 µm. ( C) Zoomed-in images of the areas indicated by yellow-dotted boxes in Panel B. These images provide a closer view of CFTR expression in the HBE cells. The scale bar represents 5 µm. (D) Magnify-processed images of CFTR ΔF508-mutated HBE cells treated with increasing doses of porosomes (0.2, 0.5, and 1 µg). This panel shows DAPI (blue), CFTR (green), and <t>SNAP23</t> (red), illustrating the expression and localization of both proteins in response to porosome treatment. The scale bar represents 5 µm in biological scale. B, C and D: The expansion factor is 3.8× (1× PBS).
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    Santa Cruz Biotechnology anti snap23

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    Image Search Results


    (A) Wide-field fluorescence images of untreated HBE cells (left) and HBE cells with CFTR ΔF508 mutation treated with increasing concentrations of porosomes (0.5, and 1 µg). The scale bar represents 50 µm. DAPI (blue) stains the nuclei, and CFTR (green) highlights the CFTR protein. ( B) Magnify-processed images of the same conditions as in Panel A, showing enhanced resolution and detail of CFTR expression. The scale bar represents 50 µm. ( C) Zoomed-in images of the areas indicated by yellow-dotted boxes in Panel B. These images provide a closer view of CFTR expression in the HBE cells. The scale bar represents 5 µm. (D) Magnify-processed images of CFTR ΔF508-mutated HBE cells treated with increasing doses of porosomes (0.2, 0.5, and 1 µg). This panel shows DAPI (blue), CFTR (green), and SNAP23 (red), illustrating the expression and localization of both proteins in response to porosome treatment. The scale bar represents 5 µm in biological scale. B, C and D: The expansion factor is 3.8× (1× PBS).

    Journal: bioRxiv

    Article Title: Porosome reconstitution therapy: A biologic rescue from cystic fibrosis

    doi: 10.1101/2024.09.11.612494

    Figure Lengend Snippet: (A) Wide-field fluorescence images of untreated HBE cells (left) and HBE cells with CFTR ΔF508 mutation treated with increasing concentrations of porosomes (0.5, and 1 µg). The scale bar represents 50 µm. DAPI (blue) stains the nuclei, and CFTR (green) highlights the CFTR protein. ( B) Magnify-processed images of the same conditions as in Panel A, showing enhanced resolution and detail of CFTR expression. The scale bar represents 50 µm. ( C) Zoomed-in images of the areas indicated by yellow-dotted boxes in Panel B. These images provide a closer view of CFTR expression in the HBE cells. The scale bar represents 5 µm. (D) Magnify-processed images of CFTR ΔF508-mutated HBE cells treated with increasing doses of porosomes (0.2, 0.5, and 1 µg). This panel shows DAPI (blue), CFTR (green), and SNAP23 (red), illustrating the expression and localization of both proteins in response to porosome treatment. The scale bar represents 5 µm in biological scale. B, C and D: The expansion factor is 3.8× (1× PBS).

    Article Snippet: Cells were incubated with a staining buffer (2X SSC, 0.2% Tween-20, 1X PBS) containing primary antibodies (1:500 dilution): mouse anti-CFTR (Invitrogen; MA1-935) and rabbit anti-SNAP23 (Invitrogen; PA5-28936) for 45 minutes to 1 hour at room temperature.

    Techniques: Fluorescence, Mutagenesis, Expressing

    Journal: eLife

    Article Title: ICAM-1 nanoclusters regulate hepatic epithelial cell polarity by leukocyte adhesion-independent control of apical actomyosin

    doi: 10.7554/eLife.89261

    Figure Lengend Snippet:

    Article Snippet: Antibody , Anti-SNAP23 (mouse monoclonal) , Santa Cruz Biotechnology , sc-374215; RRID: AB_10990315 , WB 1/1000.

    Techniques: Isolation, Transfection, Construct, Plasmid Preparation, CRISPR, Purification, Sequencing, Recombinant, Immunohistochemistry, Immunofluorescence, Cryo-EM Sample Prep, Tomography, Bioprocessing, Immunoprecipitation