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mouse anti sv2 igg antibody  (Developmental Studies Hybridoma Bank)


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    Structured Review

    Developmental Studies Hybridoma Bank mouse anti sv2 igg antibody
    Data analysis methods of expanded NMJs (A) Example of an expanded human NMJ stained with α-Bungarotoxin to label AChRs (cyan) and immunolabeled for <t>SV2</t> to visualize presynaptic vesicles (magenta). Scale bar= 4 μm. A zoomed-in region (i) illustrates the selected area for measurement. AChR width was quantified on thresholded images (ii), indicated by red bars. AChR strip length and inter-strip spacing were measured on skeletonized images (iii), with yellow bars showing strip length and blue bars indicating spacing. Scale bar in (i)= 2 μm. (B) Mouse NMJ labeled as in (A). The yellow-dotted rectangle denotes the region used for fluorescence intensity profile analysis of AChRs and SV2. Intensity profiles were generated separately for each channel. Scale bar= 4 μm. Scale bar corresponds to the physical size of the expanded sample (not adjusted to expansion factor).
    Mouse Anti Sv2 Igg Antibody, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 98/100, based on 1332 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse anti sv2 igg antibody/product/Developmental Studies Hybridoma Bank
    Average 98 stars, based on 1332 article reviews
    mouse anti sv2 igg antibody - by Bioz Stars, 2026-02
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    Images

    1) Product Images from "Protocol for applying expansion microscopy to the study of mammalian neuromuscular junctions"

    Article Title: Protocol for applying expansion microscopy to the study of mammalian neuromuscular junctions

    Journal: STAR Protocols

    doi: 10.1016/j.xpro.2025.104272

    Data analysis methods of expanded NMJs (A) Example of an expanded human NMJ stained with α-Bungarotoxin to label AChRs (cyan) and immunolabeled for SV2 to visualize presynaptic vesicles (magenta). Scale bar= 4 μm. A zoomed-in region (i) illustrates the selected area for measurement. AChR width was quantified on thresholded images (ii), indicated by red bars. AChR strip length and inter-strip spacing were measured on skeletonized images (iii), with yellow bars showing strip length and blue bars indicating spacing. Scale bar in (i)= 2 μm. (B) Mouse NMJ labeled as in (A). The yellow-dotted rectangle denotes the region used for fluorescence intensity profile analysis of AChRs and SV2. Intensity profiles were generated separately for each channel. Scale bar= 4 μm. Scale bar corresponds to the physical size of the expanded sample (not adjusted to expansion factor).
    Figure Legend Snippet: Data analysis methods of expanded NMJs (A) Example of an expanded human NMJ stained with α-Bungarotoxin to label AChRs (cyan) and immunolabeled for SV2 to visualize presynaptic vesicles (magenta). Scale bar= 4 μm. A zoomed-in region (i) illustrates the selected area for measurement. AChR width was quantified on thresholded images (ii), indicated by red bars. AChR strip length and inter-strip spacing were measured on skeletonized images (iii), with yellow bars showing strip length and blue bars indicating spacing. Scale bar in (i)= 2 μm. (B) Mouse NMJ labeled as in (A). The yellow-dotted rectangle denotes the region used for fluorescence intensity profile analysis of AChRs and SV2. Intensity profiles were generated separately for each channel. Scale bar= 4 μm. Scale bar corresponds to the physical size of the expanded sample (not adjusted to expansion factor).

    Techniques Used: Staining, Immunolabeling, Stripping Membranes, Labeling, Fluorescence, Generated



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    Developmental Studies Hybridoma Bank mouse anti sv2 igg antibody
    Data analysis methods of expanded NMJs (A) Example of an expanded human NMJ stained with α-Bungarotoxin to label AChRs (cyan) and immunolabeled for <t>SV2</t> to visualize presynaptic vesicles (magenta). Scale bar= 4 μm. A zoomed-in region (i) illustrates the selected area for measurement. AChR width was quantified on thresholded images (ii), indicated by red bars. AChR strip length and inter-strip spacing were measured on skeletonized images (iii), with yellow bars showing strip length and blue bars indicating spacing. Scale bar in (i)= 2 μm. (B) Mouse NMJ labeled as in (A). The yellow-dotted rectangle denotes the region used for fluorescence intensity profile analysis of AChRs and SV2. Intensity profiles were generated separately for each channel. Scale bar= 4 μm. Scale bar corresponds to the physical size of the expanded sample (not adjusted to expansion factor).
    Mouse Anti Sv2 Igg Antibody, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse anti sv2 igg antibody/product/Developmental Studies Hybridoma Bank
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    mouse anti sv2 igg antibody - by Bioz Stars, 2026-02
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    Developmental Studies Hybridoma Bank mouse anti sv2 igg
    Data analysis methods of expanded NMJs (A) Example of an expanded human NMJ stained with α-Bungarotoxin to label AChRs (cyan) and immunolabeled for <t>SV2</t> to visualize presynaptic vesicles (magenta). Scale bar= 4 μm. A zoomed-in region (i) illustrates the selected area for measurement. AChR width was quantified on thresholded images (ii), indicated by red bars. AChR strip length and inter-strip spacing were measured on skeletonized images (iii), with yellow bars showing strip length and blue bars indicating spacing. Scale bar in (i)= 2 μm. (B) Mouse NMJ labeled as in (A). The yellow-dotted rectangle denotes the region used for fluorescence intensity profile analysis of AChRs and SV2. Intensity profiles were generated separately for each channel. Scale bar= 4 μm. Scale bar corresponds to the physical size of the expanded sample (not adjusted to expansion factor).
    Mouse Anti Sv2 Igg, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse anti sv2 igg/product/Developmental Studies Hybridoma Bank
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    Developmental Studies Hybridoma Bank mouse anti sv2
    Data analysis methods of expanded NMJs (A) Example of an expanded human NMJ stained with α-Bungarotoxin to label AChRs (cyan) and immunolabeled for <t>SV2</t> to visualize presynaptic vesicles (magenta). Scale bar= 4 μm. A zoomed-in region (i) illustrates the selected area for measurement. AChR width was quantified on thresholded images (ii), indicated by red bars. AChR strip length and inter-strip spacing were measured on skeletonized images (iii), with yellow bars showing strip length and blue bars indicating spacing. Scale bar in (i)= 2 μm. (B) Mouse NMJ labeled as in (A). The yellow-dotted rectangle denotes the region used for fluorescence intensity profile analysis of AChRs and SV2. Intensity profiles were generated separately for each channel. Scale bar= 4 μm. Scale bar corresponds to the physical size of the expanded sample (not adjusted to expansion factor).
    Mouse Anti Sv2, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Developmental Studies Hybridoma Bank anti sv2 mouse monoclonal antibody
    Data analysis methods of expanded NMJs (A) Example of an expanded human NMJ stained with α-Bungarotoxin to label AChRs (cyan) and immunolabeled for <t>SV2</t> to visualize presynaptic vesicles (magenta). Scale bar= 4 μm. A zoomed-in region (i) illustrates the selected area for measurement. AChR width was quantified on thresholded images (ii), indicated by red bars. AChR strip length and inter-strip spacing were measured on skeletonized images (iii), with yellow bars showing strip length and blue bars indicating spacing. Scale bar in (i)= 2 μm. (B) Mouse NMJ labeled as in (A). The yellow-dotted rectangle denotes the region used for fluorescence intensity profile analysis of AChRs and SV2. Intensity profiles were generated separately for each channel. Scale bar= 4 μm. Scale bar corresponds to the physical size of the expanded sample (not adjusted to expansion factor).
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    Developmental Studies Hybridoma Bank antibodies mouse anti sv2 igg antibody
    Data analysis methods of expanded NMJs (A) Example of an expanded human NMJ stained with α-Bungarotoxin to label AChRs (cyan) and immunolabeled for <t>SV2</t> to visualize presynaptic vesicles (magenta). Scale bar= 4 μm. A zoomed-in region (i) illustrates the selected area for measurement. AChR width was quantified on thresholded images (ii), indicated by red bars. AChR strip length and inter-strip spacing were measured on skeletonized images (iii), with yellow bars showing strip length and blue bars indicating spacing. Scale bar in (i)= 2 μm. (B) Mouse NMJ labeled as in (A). The yellow-dotted rectangle denotes the region used for fluorescence intensity profile analysis of AChRs and SV2. Intensity profiles were generated separately for each channel. Scale bar= 4 μm. Scale bar corresponds to the physical size of the expanded sample (not adjusted to expansion factor).
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    Developmental Studies Hybridoma Bank mouse anti synaptic vesicle protein
    Data analysis methods of expanded NMJs (A) Example of an expanded human NMJ stained with α-Bungarotoxin to label AChRs (cyan) and immunolabeled for <t>SV2</t> to visualize presynaptic vesicles (magenta). Scale bar= 4 μm. A zoomed-in region (i) illustrates the selected area for measurement. AChR width was quantified on thresholded images (ii), indicated by red bars. AChR strip length and inter-strip spacing were measured on skeletonized images (iii), with yellow bars showing strip length and blue bars indicating spacing. Scale bar in (i)= 2 μm. (B) Mouse NMJ labeled as in (A). The yellow-dotted rectangle denotes the region used for fluorescence intensity profile analysis of AChRs and SV2. Intensity profiles were generated separately for each channel. Scale bar= 4 μm. Scale bar corresponds to the physical size of the expanded sample (not adjusted to expansion factor).
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    Developmental Studies Hybridoma Bank mouse anit sv2a antibody
    Data analysis methods of expanded NMJs (A) Example of an expanded human NMJ stained with α-Bungarotoxin to label AChRs (cyan) and immunolabeled for <t>SV2</t> to visualize presynaptic vesicles (magenta). Scale bar= 4 μm. A zoomed-in region (i) illustrates the selected area for measurement. AChR width was quantified on thresholded images (ii), indicated by red bars. AChR strip length and inter-strip spacing were measured on skeletonized images (iii), with yellow bars showing strip length and blue bars indicating spacing. Scale bar in (i)= 2 μm. (B) Mouse NMJ labeled as in (A). The yellow-dotted rectangle denotes the region used for fluorescence intensity profile analysis of AChRs and SV2. Intensity profiles were generated separately for each channel. Scale bar= 4 μm. Scale bar corresponds to the physical size of the expanded sample (not adjusted to expansion factor).
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    Image Search Results


    Data analysis methods of expanded NMJs (A) Example of an expanded human NMJ stained with α-Bungarotoxin to label AChRs (cyan) and immunolabeled for SV2 to visualize presynaptic vesicles (magenta). Scale bar= 4 μm. A zoomed-in region (i) illustrates the selected area for measurement. AChR width was quantified on thresholded images (ii), indicated by red bars. AChR strip length and inter-strip spacing were measured on skeletonized images (iii), with yellow bars showing strip length and blue bars indicating spacing. Scale bar in (i)= 2 μm. (B) Mouse NMJ labeled as in (A). The yellow-dotted rectangle denotes the region used for fluorescence intensity profile analysis of AChRs and SV2. Intensity profiles were generated separately for each channel. Scale bar= 4 μm. Scale bar corresponds to the physical size of the expanded sample (not adjusted to expansion factor).

    Journal: STAR Protocols

    Article Title: Protocol for applying expansion microscopy to the study of mammalian neuromuscular junctions

    doi: 10.1016/j.xpro.2025.104272

    Figure Lengend Snippet: Data analysis methods of expanded NMJs (A) Example of an expanded human NMJ stained with α-Bungarotoxin to label AChRs (cyan) and immunolabeled for SV2 to visualize presynaptic vesicles (magenta). Scale bar= 4 μm. A zoomed-in region (i) illustrates the selected area for measurement. AChR width was quantified on thresholded images (ii), indicated by red bars. AChR strip length and inter-strip spacing were measured on skeletonized images (iii), with yellow bars showing strip length and blue bars indicating spacing. Scale bar in (i)= 2 μm. (B) Mouse NMJ labeled as in (A). The yellow-dotted rectangle denotes the region used for fluorescence intensity profile analysis of AChRs and SV2. Intensity profiles were generated separately for each channel. Scale bar= 4 μm. Scale bar corresponds to the physical size of the expanded sample (not adjusted to expansion factor).

    Article Snippet: Mouse anti-SV2 IgG antibody (1:50 dilution) , Developmental Studies Hybridoma Bank , Cat#2315387; RRID: AB-2315387.

    Techniques: Staining, Immunolabeling, Stripping Membranes, Labeling, Fluorescence, Generated