Review



fibronectin crosslinking  (Cytoskeleton Inc)


Bioz Verified Symbol Cytoskeleton Inc is a verified supplier
Bioz Manufacturer Symbol Cytoskeleton Inc manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
    • 93
      Buy from Supplier

    Structured Review

    Cytoskeleton Inc fibronectin crosslinking
    Schematic overview of extracellular matrix and its major components. Although the ECM composition varies depending on the tissue, the matrix is mainly composed of a variety of fibrous proteins (collagen, elastin, <t>fibronectin,</t> and laminin) and polysaccharides that are secreted locally and assembled into an organized meshwork in close association with the surface of the cell that produced them.
    Fibronectin Crosslinking, supplied by Cytoskeleton Inc, used in various techniques. Bioz Stars score: 93/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fibronectin+crosslinking/pmc08308089-1-31-41?v=Cytoskeleton+Inc
    Average 93 stars, based on 7 article reviews
    fibronectin crosslinking - by Bioz Stars, 2026-07
    93/100 stars

    Images

    1) Product Images from "Optical Microscopy and the Extracellular Matrix Structure: A Review"

    Article Title: Optical Microscopy and the Extracellular Matrix Structure: A Review

    Journal: Cells

    doi: 10.3390/cells10071760

    Schematic overview of extracellular matrix and its major components. Although the ECM composition varies depending on the tissue, the matrix is mainly composed of a variety of fibrous proteins (collagen, elastin, fibronectin, and laminin) and polysaccharides that are secreted locally and assembled into an organized meshwork in close association with the surface of the cell that produced them.
    Figure Legend Snippet: Schematic overview of extracellular matrix and its major components. Although the ECM composition varies depending on the tissue, the matrix is mainly composed of a variety of fibrous proteins (collagen, elastin, fibronectin, and laminin) and polysaccharides that are secreted locally and assembled into an organized meshwork in close association with the surface of the cell that produced them.

    Techniques Used: Produced

    The most commonly used linear fluorescence-based super-resolution microscopy modalities to assess ECM components.
    Figure Legend Snippet: The most commonly used linear fluorescence-based super-resolution microscopy modalities to assess ECM components.

    Techniques Used: Fluorescence, Super-Resolution Microscopy, Imaging, In Vivo, Control, Modification, Microscopy

    Representative images of different ECM components acquired by ( A ) WFFM, ( B ) LSCM, ( C ) STED/GSD, ( D , E ) PALM, and ( F ) STORM. ( A ) Shows a widefield fluorescence image of fibroblasts and matrix followed by images of Alexa-647-labeled fibronectin and antibody-stained collagen I alone. Scale bar, 100 μm . ( B ) Image obtained by confocal microscopy of fibronectin deposition and localization in 3D co-cultures of human breast cancer cells and human dermal fibroblasts. Cultures were labelled to visualize actin (red), fibronectin (green), and cell nuclei (blue). Scale bar, 50 μm . ( C ) Higher magnification SUSHI (super-resolution shadow imaging) images of cell bodies and neuropil in CA1 area. Scale bar in top, 4 mm; middle, 5 mm; bottom, 2 mm . ( D ) Schematic of sample setup for iPALM imaging of migratory Jurkat T-lymphocytes adhered to ICAM-1 or fibronectin-coated lower coverslips, with gold nanorod fiducial markers (orange spheres) . ( E ) Representative iPALM renderings of Jurkat cells expressing mEOS3.2-LFA-1 fusion, mEOS3.2-CAAX, or LifeAct-mEos3.2. Scale bars, 5 mm . ( F ) STORM images of mineralized collagen fibrils at an early stage (top). Representative Z-dimension slices of the STORM images (bottom). Amorphous calcium phosphate (ACP) preferentially aggregates around purple in the intrafibrillar compartments, which represent chondroitin sulfate (CS) in CS-collagen fibril. Scale bar: 500 nm . Images reproduced with permission from [ , , , , ].
    Figure Legend Snippet: Representative images of different ECM components acquired by ( A ) WFFM, ( B ) LSCM, ( C ) STED/GSD, ( D , E ) PALM, and ( F ) STORM. ( A ) Shows a widefield fluorescence image of fibroblasts and matrix followed by images of Alexa-647-labeled fibronectin and antibody-stained collagen I alone. Scale bar, 100 μm . ( B ) Image obtained by confocal microscopy of fibronectin deposition and localization in 3D co-cultures of human breast cancer cells and human dermal fibroblasts. Cultures were labelled to visualize actin (red), fibronectin (green), and cell nuclei (blue). Scale bar, 50 μm . ( C ) Higher magnification SUSHI (super-resolution shadow imaging) images of cell bodies and neuropil in CA1 area. Scale bar in top, 4 mm; middle, 5 mm; bottom, 2 mm . ( D ) Schematic of sample setup for iPALM imaging of migratory Jurkat T-lymphocytes adhered to ICAM-1 or fibronectin-coated lower coverslips, with gold nanorod fiducial markers (orange spheres) . ( E ) Representative iPALM renderings of Jurkat cells expressing mEOS3.2-LFA-1 fusion, mEOS3.2-CAAX, or LifeAct-mEos3.2. Scale bars, 5 mm . ( F ) STORM images of mineralized collagen fibrils at an early stage (top). Representative Z-dimension slices of the STORM images (bottom). Amorphous calcium phosphate (ACP) preferentially aggregates around purple in the intrafibrillar compartments, which represent chondroitin sulfate (CS) in CS-collagen fibril. Scale bar: 500 nm . Images reproduced with permission from [ , , , , ].

    Techniques Used: Fluorescence, Labeling, Staining, Confocal Microscopy, Imaging, Expressing

    Representative examples of applications of different microscopy modalities to assess ECM main components.
    Figure Legend Snippet: Representative examples of applications of different microscopy modalities to assess ECM main components.

    Techniques Used: Microscopy, Imaging



    Similar Products

    fibronectin crosslinking  (Cytoskeleton Inc)
    93
    Cytoskeleton Inc fibronectin crosslinking
    Schematic overview of extracellular matrix and its major components. Although the ECM composition varies depending on the tissue, the matrix is mainly composed of a variety of fibrous proteins (collagen, elastin, <t>fibronectin,</t> and laminin) and polysaccharides that are secreted locally and assembled into an organized meshwork in close association with the surface of the cell that produced them.
    Fibronectin Crosslinking, supplied by Cytoskeleton Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fibronectin+crosslinking/pmc08308089-1-31-41?v=Cytoskeleton+Inc
    Average 93 stars, based on 1 article reviews
    fibronectin crosslinking - by Bioz Stars, 2026-07
    93/100 stars
    		  Buy from Supplier

    Image Search Results


    Schematic overview of extracellular matrix and its major components. Although the ECM composition varies depending on the tissue, the matrix is mainly composed of a variety of fibrous proteins (collagen, elastin, fibronectin, and laminin) and polysaccharides that are secreted locally and assembled into an organized meshwork in close association with the surface of the cell that produced them.

    Journal: Cells

    Article Title: Optical Microscopy and the Extracellular Matrix Structure: A Review

    doi: 10.3390/cells10071760

    Figure Lengend Snippet: Schematic overview of extracellular matrix and its major components. Although the ECM composition varies depending on the tissue, the matrix is mainly composed of a variety of fibrous proteins (collagen, elastin, fibronectin, and laminin) and polysaccharides that are secreted locally and assembled into an organized meshwork in close association with the surface of the cell that produced them.

    Article Snippet: TIRFM , Good SNR due to low penetration depth of the evanescent field Reduced photobleaching , Sectioning is confined to a single-plane immediately adjacent to the cover glass or slide , Fibronectin Crosslinking of ECM fibrillar proteins Cell adhesion points Endo-exocytosis Cytoskeleton dynamics.

    Techniques: Produced

    The most commonly used linear fluorescence-based super-resolution microscopy modalities to assess ECM components.

    Journal: Cells

    Article Title: Optical Microscopy and the Extracellular Matrix Structure: A Review

    doi: 10.3390/cells10071760

    Figure Lengend Snippet: The most commonly used linear fluorescence-based super-resolution microscopy modalities to assess ECM components.

    Article Snippet: TIRFM , Good SNR due to low penetration depth of the evanescent field Reduced photobleaching , Sectioning is confined to a single-plane immediately adjacent to the cover glass or slide , Fibronectin Crosslinking of ECM fibrillar proteins Cell adhesion points Endo-exocytosis Cytoskeleton dynamics.

    Techniques: Fluorescence, Super-Resolution Microscopy, Imaging, In Vivo, Control, Modification, Microscopy

    Representative images of different ECM components acquired by ( A ) WFFM, ( B ) LSCM, ( C ) STED/GSD, ( D , E ) PALM, and ( F ) STORM. ( A ) Shows a widefield fluorescence image of fibroblasts and matrix followed by images of Alexa-647-labeled fibronectin and antibody-stained collagen I alone. Scale bar, 100 μm . ( B ) Image obtained by confocal microscopy of fibronectin deposition and localization in 3D co-cultures of human breast cancer cells and human dermal fibroblasts. Cultures were labelled to visualize actin (red), fibronectin (green), and cell nuclei (blue). Scale bar, 50 μm . ( C ) Higher magnification SUSHI (super-resolution shadow imaging) images of cell bodies and neuropil in CA1 area. Scale bar in top, 4 mm; middle, 5 mm; bottom, 2 mm . ( D ) Schematic of sample setup for iPALM imaging of migratory Jurkat T-lymphocytes adhered to ICAM-1 or fibronectin-coated lower coverslips, with gold nanorod fiducial markers (orange spheres) . ( E ) Representative iPALM renderings of Jurkat cells expressing mEOS3.2-LFA-1 fusion, mEOS3.2-CAAX, or LifeAct-mEos3.2. Scale bars, 5 mm . ( F ) STORM images of mineralized collagen fibrils at an early stage (top). Representative Z-dimension slices of the STORM images (bottom). Amorphous calcium phosphate (ACP) preferentially aggregates around purple in the intrafibrillar compartments, which represent chondroitin sulfate (CS) in CS-collagen fibril. Scale bar: 500 nm . Images reproduced with permission from [ , , , , ].

    Journal: Cells

    Article Title: Optical Microscopy and the Extracellular Matrix Structure: A Review

    doi: 10.3390/cells10071760

    Figure Lengend Snippet: Representative images of different ECM components acquired by ( A ) WFFM, ( B ) LSCM, ( C ) STED/GSD, ( D , E ) PALM, and ( F ) STORM. ( A ) Shows a widefield fluorescence image of fibroblasts and matrix followed by images of Alexa-647-labeled fibronectin and antibody-stained collagen I alone. Scale bar, 100 μm . ( B ) Image obtained by confocal microscopy of fibronectin deposition and localization in 3D co-cultures of human breast cancer cells and human dermal fibroblasts. Cultures were labelled to visualize actin (red), fibronectin (green), and cell nuclei (blue). Scale bar, 50 μm . ( C ) Higher magnification SUSHI (super-resolution shadow imaging) images of cell bodies and neuropil in CA1 area. Scale bar in top, 4 mm; middle, 5 mm; bottom, 2 mm . ( D ) Schematic of sample setup for iPALM imaging of migratory Jurkat T-lymphocytes adhered to ICAM-1 or fibronectin-coated lower coverslips, with gold nanorod fiducial markers (orange spheres) . ( E ) Representative iPALM renderings of Jurkat cells expressing mEOS3.2-LFA-1 fusion, mEOS3.2-CAAX, or LifeAct-mEos3.2. Scale bars, 5 mm . ( F ) STORM images of mineralized collagen fibrils at an early stage (top). Representative Z-dimension slices of the STORM images (bottom). Amorphous calcium phosphate (ACP) preferentially aggregates around purple in the intrafibrillar compartments, which represent chondroitin sulfate (CS) in CS-collagen fibril. Scale bar: 500 nm . Images reproduced with permission from [ , , , , ].

    Article Snippet: TIRFM , Good SNR due to low penetration depth of the evanescent field Reduced photobleaching , Sectioning is confined to a single-plane immediately adjacent to the cover glass or slide , Fibronectin Crosslinking of ECM fibrillar proteins Cell adhesion points Endo-exocytosis Cytoskeleton dynamics.

    Techniques: Fluorescence, Labeling, Staining, Confocal Microscopy, Imaging, Expressing

    Representative examples of applications of different microscopy modalities to assess ECM main components.

    Journal: Cells

    Article Title: Optical Microscopy and the Extracellular Matrix Structure: A Review

    doi: 10.3390/cells10071760

    Figure Lengend Snippet: Representative examples of applications of different microscopy modalities to assess ECM main components.

    Article Snippet: TIRFM , Good SNR due to low penetration depth of the evanescent field Reduced photobleaching , Sectioning is confined to a single-plane immediately adjacent to the cover glass or slide , Fibronectin Crosslinking of ECM fibrillar proteins Cell adhesion points Endo-exocytosis Cytoskeleton dynamics.

    Techniques: Microscopy, Imaging