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snap surface af647  (New England Biolabs)


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    Structured Review

    New England Biolabs snap surface af647
    Snap Surface Af647, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 96/100, based on 325 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/snap surface af647/product/New England Biolabs
    Average 96 stars, based on 325 article reviews
    snap surface af647 - by Bioz Stars, 2026-03
    96/100 stars

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    Image Search Results


    Journal: bioRxiv

    Article Title: High Refractive Index Imaging Buffer for Dual Color 3D SMLM Imaging of Thick Samples

    doi: 10.1101/2024.04.30.591648

    Figure Lengend Snippet:

    Article Snippet: We labeled Nup96-SNAP with SNAP-tag ligand O 6 -benzylguanine conjugated AF647 (BG-AF647, S9136S, New England Biolabs) as described else ( ).

    Techniques:

    (a-c) Representative images of microtubules (anti-β-tubulin/CF680) and the outer mitochondrial membrane (anti- Tom20/AF647) in CUBIC-R+ (a), 3-PM (b) and WI (c) buffers. Color bar denotes the z position. (d) The side view of the white dashed regions in (a-c). The white arrows indicate the mitochondria-microtubule contacts, while the red arrows denote the different layers of microtubule filaments. (e, f) FRC curves of microtubule (e) or mitochondria (f) in regions corresponding to the bottom panels of (a-c). Scale bars: 2 μm (a-c), 200 nm (d).

    Journal: bioRxiv

    Article Title: High Refractive Index Imaging Buffer for Dual Color 3D SMLM Imaging of Thick Samples

    doi: 10.1101/2024.04.30.591648

    Figure Lengend Snippet: (a-c) Representative images of microtubules (anti-β-tubulin/CF680) and the outer mitochondrial membrane (anti- Tom20/AF647) in CUBIC-R+ (a), 3-PM (b) and WI (c) buffers. Color bar denotes the z position. (d) The side view of the white dashed regions in (a-c). The white arrows indicate the mitochondria-microtubule contacts, while the red arrows denote the different layers of microtubule filaments. (e, f) FRC curves of microtubule (e) or mitochondria (f) in regions corresponding to the bottom panels of (a-c). Scale bars: 2 μm (a-c), 200 nm (d).

    Article Snippet: We labeled Nup96-SNAP with SNAP-tag ligand O 6 -benzylguanine conjugated AF647 (BG-AF647, S9136S, New England Biolabs) as described else ( ).

    Techniques: Membrane

    (a, c) Dual-color 3D SMLM images of microtubules (anti-β-tubulin/CF680) and the outer mitochondrial membrane (anti-Tom20/AF647) in CUBIC-R+ (a) and WI (c) buffers. Color bars denote the z position. (b, d) The side view of the white dashed regions in (a, c). The white arrows indicate the mitochondria-microtubule contacts, while the red arrows denote the different layers of microtubule filaments. Scale bars: 2 μm (a, c), 200 nm (b, d).

    Journal: bioRxiv

    Article Title: High Refractive Index Imaging Buffer for Dual Color 3D SMLM Imaging of Thick Samples

    doi: 10.1101/2024.04.30.591648

    Figure Lengend Snippet: (a, c) Dual-color 3D SMLM images of microtubules (anti-β-tubulin/CF680) and the outer mitochondrial membrane (anti-Tom20/AF647) in CUBIC-R+ (a) and WI (c) buffers. Color bars denote the z position. (b, d) The side view of the white dashed regions in (a, c). The white arrows indicate the mitochondria-microtubule contacts, while the red arrows denote the different layers of microtubule filaments. Scale bars: 2 μm (a, c), 200 nm (b, d).

    Article Snippet: We labeled Nup96-SNAP with SNAP-tag ligand O 6 -benzylguanine conjugated AF647 (BG-AF647, S9136S, New England Biolabs) as described else ( ).

    Techniques: Membrane

    (a) Three mouse brain tissue slices (30 μm thick) were imbedded in CUBIC-R+, 3-PM and PBS for 10 min before taking photos, respectively. (b) Diagram of experimental setup for deep imaging of NPCs. (c, d) 3D SMLM images of Nup96 labeled by AF647 in CUBIC-R+ (c) and 3-PM (d) buffers. The right panels show zoomed images for regions in white, and the color bar show the z position. (e) The side view images of the white dashed regions in (c, d). (f) Plots of distance between the rings versus the z position for Nup96 in different depths and buffers. (g) Scatter plots of the photon number (left) and ELE (right) for Nup96 in oil-index buffers. Each symbol corresponds to one cell nucleus. Horizontal bars and errors show the means and SD, respectively. Scale bars: 2 μm (c, d), 200 nm (e).

    Journal: bioRxiv

    Article Title: High Refractive Index Imaging Buffer for Dual Color 3D SMLM Imaging of Thick Samples

    doi: 10.1101/2024.04.30.591648

    Figure Lengend Snippet: (a) Three mouse brain tissue slices (30 μm thick) were imbedded in CUBIC-R+, 3-PM and PBS for 10 min before taking photos, respectively. (b) Diagram of experimental setup for deep imaging of NPCs. (c, d) 3D SMLM images of Nup96 labeled by AF647 in CUBIC-R+ (c) and 3-PM (d) buffers. The right panels show zoomed images for regions in white, and the color bar show the z position. (e) The side view images of the white dashed regions in (c, d). (f) Plots of distance between the rings versus the z position for Nup96 in different depths and buffers. (g) Scatter plots of the photon number (left) and ELE (right) for Nup96 in oil-index buffers. Each symbol corresponds to one cell nucleus. Horizontal bars and errors show the means and SD, respectively. Scale bars: 2 μm (c, d), 200 nm (e).

    Article Snippet: We labeled Nup96-SNAP with SNAP-tag ligand O 6 -benzylguanine conjugated AF647 (BG-AF647, S9136S, New England Biolabs) as described else ( ).

    Techniques: Imaging, Labeling