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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
    98/100 stars

    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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    98
    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
    Average 98 stars, based on 1 article reviews
    mouse anti sv2 igg antibody - by Bioz Stars, 2026-02
    98/100 stars
      Buy from Supplier

    98
    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
    Average 98 stars, based on 1 article reviews
    mouse anti sv2 igg - by Bioz Stars, 2026-02
    98/100 stars
      Buy from Supplier

    98
    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).
    Antibodies 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/antibodies mouse anti sv2 igg antibody/product/Developmental Studies Hybridoma Bank
    Average 98 stars, based on 1 article reviews
    antibodies mouse anti sv2 igg antibody - by Bioz Stars, 2026-02
    98/100 stars
      Buy from Supplier

    98
    Developmental Studies Hybridoma Bank anti mouse igg sv2 antibody
    Injection of ATG poly-GR evokes apoptosis and aberrant motor neuron axon morphology in 1-4-dpf zebrafish embryos. (A) Maximum projection of z -stack images of the SecA5 fluorescent reporter line (green) embryos 48 h after injection with 10 pg ATG poly-GR, 10 pg TAG poly-GR or 400 pg mCherry only. (B) Quantification of z -stack images of the SecA5 fluorescent reporter line embryos after injection with 10 pg ATG poly-GR, 10 pg TAG poly-GR or 400 pg mCherry only at 1-4 dpf. N =minimum of ten fish per group (mean±s.e.m.). P <0.0001 (Kruskal–Wallis test). * P <0.05, *** P <0.0001 (Dunn's post-hoc multiple comparison test), differences of ATG poly-GR-injected fish compared to 10 pg TAG poly-GR and mCherry only at 1-4 dpf. (C) Synaptic vesicle <t>(SV2)</t> in combination with α-bungarotoxin (BTX) staining demonstrates aberrant axonal protrusions in the tail of 2-dpf wild-type AB embryos after injection with 10 pg ATG poly-GR compared to 10 pg TAG poly-GR and 400 pg mCherry only. n =10 per group (mean±s.e.m.). (D) Fluorescence of SV2 staining was measured for five fish/group and three neurites per fish, and was significantly reduced in 10 pg ATG poly-GR-injected embryos. P <0.0001 (one-tailed t -test with Welch's correction). Scale bars: 100 µm.
    Anti Mouse Igg Sv2 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/anti mouse igg sv2 antibody/product/Developmental Studies Hybridoma Bank
    Average 98 stars, based on 1 article reviews
    anti mouse igg sv2 antibody - by Bioz Stars, 2026-02
    98/100 stars
      Buy from Supplier

    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

    Injection of ATG poly-GR evokes apoptosis and aberrant motor neuron axon morphology in 1-4-dpf zebrafish embryos. (A) Maximum projection of z -stack images of the SecA5 fluorescent reporter line (green) embryos 48 h after injection with 10 pg ATG poly-GR, 10 pg TAG poly-GR or 400 pg mCherry only. (B) Quantification of z -stack images of the SecA5 fluorescent reporter line embryos after injection with 10 pg ATG poly-GR, 10 pg TAG poly-GR or 400 pg mCherry only at 1-4 dpf. N =minimum of ten fish per group (mean±s.e.m.). P <0.0001 (Kruskal–Wallis test). * P <0.05, *** P <0.0001 (Dunn's post-hoc multiple comparison test), differences of ATG poly-GR-injected fish compared to 10 pg TAG poly-GR and mCherry only at 1-4 dpf. (C) Synaptic vesicle (SV2) in combination with α-bungarotoxin (BTX) staining demonstrates aberrant axonal protrusions in the tail of 2-dpf wild-type AB embryos after injection with 10 pg ATG poly-GR compared to 10 pg TAG poly-GR and 400 pg mCherry only. n =10 per group (mean±s.e.m.). (D) Fluorescence of SV2 staining was measured for five fish/group and three neurites per fish, and was significantly reduced in 10 pg ATG poly-GR-injected embryos. P <0.0001 (one-tailed t -test with Welch's correction). Scale bars: 100 µm.

    Journal: Disease Models & Mechanisms

    Article Title: Reduction of oxidative stress suppresses poly-GR-mediated toxicity in zebrafish embryos

    doi: 10.1242/dmm.049092

    Figure Lengend Snippet: Injection of ATG poly-GR evokes apoptosis and aberrant motor neuron axon morphology in 1-4-dpf zebrafish embryos. (A) Maximum projection of z -stack images of the SecA5 fluorescent reporter line (green) embryos 48 h after injection with 10 pg ATG poly-GR, 10 pg TAG poly-GR or 400 pg mCherry only. (B) Quantification of z -stack images of the SecA5 fluorescent reporter line embryos after injection with 10 pg ATG poly-GR, 10 pg TAG poly-GR or 400 pg mCherry only at 1-4 dpf. N =minimum of ten fish per group (mean±s.e.m.). P <0.0001 (Kruskal–Wallis test). * P <0.05, *** P <0.0001 (Dunn's post-hoc multiple comparison test), differences of ATG poly-GR-injected fish compared to 10 pg TAG poly-GR and mCherry only at 1-4 dpf. (C) Synaptic vesicle (SV2) in combination with α-bungarotoxin (BTX) staining demonstrates aberrant axonal protrusions in the tail of 2-dpf wild-type AB embryos after injection with 10 pg ATG poly-GR compared to 10 pg TAG poly-GR and 400 pg mCherry only. n =10 per group (mean±s.e.m.). (D) Fluorescence of SV2 staining was measured for five fish/group and three neurites per fish, and was significantly reduced in 10 pg ATG poly-GR-injected embryos. P <0.0001 (one-tailed t -test with Welch's correction). Scale bars: 100 µm.

    Article Snippet: Subsequently, fish were stained for 30 min with 1 μg/ml α-bungarotoxin-TRITC (Invitrogen), washed with PBS and incubated overnight at 4°C with the anti-mouse IgG SV2 antibody (1:200, AB231587, Developmental Studies Hybridoma Bank, University of Iowa).

    Techniques: Injection, Comparison, Staining, Fluorescence, One-tailed Test