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fibronectin ch296  (Kamada)

 
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    Kamada fibronectin ch296
    Fibronectin Ch296, supplied by Kamada, 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/product/fibronectin+ch296/fibronectin+ch296/pm38372136-844-43-18
    Average 90 stars, based on 1 article reviews
    fibronectin ch296 - by Bioz Stars, 2026-09
    90/100 stars

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    other:

    Article Title: The role of fibronectin in mediating cell migration.
    Article Snippet: Fibronectin (FN) is a major extracellular matrix (ECM) protein involved in a wide range of physiological processes, including cell migration.. These FN-mediated cell migration events are essential to processes such as wound repair, cancer metastasis, and vertebrate development.. This review synthesizes mainly current literature to provide an overview of the mechanoregulatory role of FN-mediated cell migration.

    Article Title: Extracellular Matrix Containing in vitro Three-dimensional Tumor Models in Photodynamic Therapy-related Research.
    Article Snippet: Three-dimensional (3D) tumour models have been intensively evaluated for their use in cancer research and there is a strong rationale behind using 3D cell cultures in photodynamic therapy (PDT)-related experimentation.. In this contribution, it is explained why 3D cell cultures containing extracellular matrix (ECM) are preferred for this purpose.. Results of experimental studies utilizing



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    ( A ) GFP vpr labeled vector particles were allowed to settle on glass slides in the absence (top) or presence (bottom) of recombinant fibronectin fragment, <t>CH296,</t> stained with anti-VSV-G antibody and Alexa Fluor 647 anti-mouse secondary antibody, and visualized via deconvolution microscopy. ( B ) Particles either counted as “individual” (gray bars) or as “aggregate” (black bars) if 2 or more individual particles were observed to occupy contiguous space. Significance was determined by performing a Student’s 2-tailed t-test , assuming unequal variance between groups. ( C ) GFP vpr labeled particles were allowed to settle on glass slides in the absence (top) or presence (bottom) of 8 µg/ml protamine sulfate. ( D ) Particles either counted as “individual” (gray bars) or as “aggregate” (black bars) if 2 or more individual particles were observed to occupy contiguous space. Asterisk indicates that data set for “(-PS) control is the same from (B), “(-FN)” control. Significance was determined by performing a Student’s 2-tailed t-test , assuming unequal variance between groups. ( E ) Jurkat (top panels) and 293T cells (bottom panels) were exposed to GFP vpr vector particles (green) for 1 hour at 37C, washed, and fixed with 4% paraformaldehyde. Cells were stained with phalloidin (red) and anti-VSV-G antibody (magenta), followed by staining with anti-rabbit Alexa Fluor 647 (blue), and imaging via deconvolution microscopy. ( F ) Particles either counted as “individual” (gray bars) or as “aggregate” (black bars) if 2 or more individual particles were observed to occupy contiguous space. Significance was determined by performing a Student’s 2-tailed t-test , assuming unequal variance between groups.
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    Image Search Results


    ( A ) GFP vpr labeled vector particles were allowed to settle on glass slides in the absence (top) or presence (bottom) of recombinant fibronectin fragment, CH296, stained with anti-VSV-G antibody and Alexa Fluor 647 anti-mouse secondary antibody, and visualized via deconvolution microscopy. ( B ) Particles either counted as “individual” (gray bars) or as “aggregate” (black bars) if 2 or more individual particles were observed to occupy contiguous space. Significance was determined by performing a Student’s 2-tailed t-test , assuming unequal variance between groups. ( C ) GFP vpr labeled particles were allowed to settle on glass slides in the absence (top) or presence (bottom) of 8 µg/ml protamine sulfate. ( D ) Particles either counted as “individual” (gray bars) or as “aggregate” (black bars) if 2 or more individual particles were observed to occupy contiguous space. Asterisk indicates that data set for “(-PS) control is the same from (B), “(-FN)” control. Significance was determined by performing a Student’s 2-tailed t-test , assuming unequal variance between groups. ( E ) Jurkat (top panels) and 293T cells (bottom panels) were exposed to GFP vpr vector particles (green) for 1 hour at 37C, washed, and fixed with 4% paraformaldehyde. Cells were stained with phalloidin (red) and anti-VSV-G antibody (magenta), followed by staining with anti-rabbit Alexa Fluor 647 (blue), and imaging via deconvolution microscopy. ( F ) Particles either counted as “individual” (gray bars) or as “aggregate” (black bars) if 2 or more individual particles were observed to occupy contiguous space. Significance was determined by performing a Student’s 2-tailed t-test , assuming unequal variance between groups.

    Journal: PLoS ONE

    Article Title: Cell- Cell Transmission of VSV-G Pseudotyped Lentivector Particles

    doi: 10.1371/journal.pone.0074925

    Figure Lengend Snippet: ( A ) GFP vpr labeled vector particles were allowed to settle on glass slides in the absence (top) or presence (bottom) of recombinant fibronectin fragment, CH296, stained with anti-VSV-G antibody and Alexa Fluor 647 anti-mouse secondary antibody, and visualized via deconvolution microscopy. ( B ) Particles either counted as “individual” (gray bars) or as “aggregate” (black bars) if 2 or more individual particles were observed to occupy contiguous space. Significance was determined by performing a Student’s 2-tailed t-test , assuming unequal variance between groups. ( C ) GFP vpr labeled particles were allowed to settle on glass slides in the absence (top) or presence (bottom) of 8 µg/ml protamine sulfate. ( D ) Particles either counted as “individual” (gray bars) or as “aggregate” (black bars) if 2 or more individual particles were observed to occupy contiguous space. Asterisk indicates that data set for “(-PS) control is the same from (B), “(-FN)” control. Significance was determined by performing a Student’s 2-tailed t-test , assuming unequal variance between groups. ( E ) Jurkat (top panels) and 293T cells (bottom panels) were exposed to GFP vpr vector particles (green) for 1 hour at 37C, washed, and fixed with 4% paraformaldehyde. Cells were stained with phalloidin (red) and anti-VSV-G antibody (magenta), followed by staining with anti-rabbit Alexa Fluor 647 (blue), and imaging via deconvolution microscopy. ( F ) Particles either counted as “individual” (gray bars) or as “aggregate” (black bars) if 2 or more individual particles were observed to occupy contiguous space. Significance was determined by performing a Student’s 2-tailed t-test , assuming unequal variance between groups.

    Article Snippet: Experiments involving fibronectin fragment CH296 (Takara Mirus, Madison, WI) used a final concentration of 5 µg/ml, unless otherwise noted.

    Techniques: Labeling, Plasmid Preparation, Recombinant, Staining, Microscopy, Imaging