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linescan tool  (MetaMorph Inc)

 
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    MetaMorph Inc linescan tool
    Linescan Tool, supplied by MetaMorph Inc, 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/linescan+tool/linescan+tool/pmc10990490-340-27-26
    Average 90 stars, based on 1 article reviews
    linescan tool - by Bioz Stars, 2026-09
    90/100 stars

    Images

    Related Articles

    Fluorescence:

    Article Title: Cell cycle control of spindle pole body duplication and splitting by Sfi1 and Cdc31 in fission yeast.
    Article Snippet: 1 Cell Cycle Control of Spindle Pole Body Duplication and Splitting by Sfi1 and Cdc31 in fission yeast Imène B. Bouhlel*, Midori Ohta*, Adeline Mayeux*, Nicole Bordes, Florent Dingli, Jérôme Boulanger, Guilhem Velve Casquillas, Damarys Loew, Phong T. Tran, Masamitsu Sato and Anne Paoletti# Institut Curie, Centre de Recherche F-75248 Paris, France.. CNRS UMR144 F-75248 Paris, France Waseda University, Tokyo, Japan current address: Center for Frontier Research, National Institute of Genetics Mishima, Japan 5 current address: ELVESYS Microfluidic Innovation Center, 75009 Paris

    Article Title: Regulation of dynamic polarity switching in bacteria by a Ras-like G-protein and its cognate GAP
    Article Snippet: .. The linescan tool in Metamorph 7.0r2 was used to determine the position of the maximum fluorescence signal in a cell. ..

    Article Title: Activity-dependent mitochondrial ROS signaling regulates recruitment of glutamate receptors to synapses
    Article Snippet: .. Analysis of the fluorescence before photobleaching was analyzed by creating a data file (.log) of fluorescence values along the bleached region of the AVA neurite using MetaMorph’s linescan tool (line width = 20 pixels). .. The resultant output file was analyzed using a custom MATLAB (R2021a) script to obtain the average area of fluorescent puncta (area under the peak).

    Article Title: Endogenous species of mammalian nonmuscle myosin IIA and IIB include activated monomers and heteropolymers
    Article Snippet: .. The linescan tool in Metamorph was used to obtain fluorescence intensity profiles from background-subtracted images along 3 μm wide lines drawn perpendicular the cell edge and crossing the lamellipodium, lamella, and cell body (perinuclear region). ..

    Antiviral Assay:

    Article Title: Activity-dependent mitochondrial ROS signaling regulates recruitment of glutamate receptors to synapses
    Article Snippet: .. Analysis of the fluorescence before photobleaching was analyzed by creating a data file (.log) of fluorescence values along the bleached region of the AVA neurite using MetaMorph’s linescan tool (line width = 20 pixels). .. The resultant output file was analyzed using a custom MATLAB (R2021a) script to obtain the average area of fluorescent puncta (area under the peak).



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    Immunofluorescence shows co-localization of ADAMTS-1 and nucleophosmin in MCF-10A, MCF-7 and MDA-MB-231 cell lines (A). MDA-MB-231 image used for colocalization analysis (B), with the white line used to generate the <t>linescan</t> plot (C). Linescan profiles display a clear overlap between ADAMTS-1 (Red) and nucleophosmin (Green). The colocalization color map is illustrated in C, where hot colors represent positive correlation (colocalization), and cold colors represent exclusion. Scatter plot (D) of ADAMTS-1 (red, x-axis) and nucleophosmin (green, y-axis) with the linear regression line. Points of scatterplot cluster around regression line. ADAMTS-1 (red), nucleophosmin (green) and nuclei (blue). Scale bar, 5 μm.
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    Immunofluorescence shows co-localization of ADAMTS-1 and nucleophosmin in MCF-10A, MCF-7 and MDA-MB-231 cell lines (A). MDA-MB-231 image used for colocalization analysis (B), with the white line used to generate the <t>linescan</t> plot (C). Linescan profiles display a clear overlap between ADAMTS-1 (Red) and nucleophosmin (Green). The colocalization color map is illustrated in C, where hot colors represent positive correlation (colocalization), and cold colors represent exclusion. Scatter plot (D) of ADAMTS-1 (red, x-axis) and nucleophosmin (green, y-axis) with the linear regression line. Points of scatterplot cluster around regression line. ADAMTS-1 (red), nucleophosmin (green) and nuclei (blue). Scale bar, 5 μm.
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    Image Search Results


    Immunofluorescence shows co-localization of ADAMTS-1 and nucleophosmin in MCF-10A, MCF-7 and MDA-MB-231 cell lines (A). MDA-MB-231 image used for colocalization analysis (B), with the white line used to generate the linescan plot (C). Linescan profiles display a clear overlap between ADAMTS-1 (Red) and nucleophosmin (Green). The colocalization color map is illustrated in C, where hot colors represent positive correlation (colocalization), and cold colors represent exclusion. Scatter plot (D) of ADAMTS-1 (red, x-axis) and nucleophosmin (green, y-axis) with the linear regression line. Points of scatterplot cluster around regression line. ADAMTS-1 (red), nucleophosmin (green) and nuclei (blue). Scale bar, 5 μm.

    Journal: PLoS ONE

    Article Title: ADAMTS-1 Is Found in the Nuclei of Normal and Tumoral Breast Cells

    doi: 10.1371/journal.pone.0165061

    Figure Lengend Snippet: Immunofluorescence shows co-localization of ADAMTS-1 and nucleophosmin in MCF-10A, MCF-7 and MDA-MB-231 cell lines (A). MDA-MB-231 image used for colocalization analysis (B), with the white line used to generate the linescan plot (C). Linescan profiles display a clear overlap between ADAMTS-1 (Red) and nucleophosmin (Green). The colocalization color map is illustrated in C, where hot colors represent positive correlation (colocalization), and cold colors represent exclusion. Scatter plot (D) of ADAMTS-1 (red, x-axis) and nucleophosmin (green, y-axis) with the linear regression line. Points of scatterplot cluster around regression line. ADAMTS-1 (red), nucleophosmin (green) and nuclei (blue). Scale bar, 5 μm.

    Article Snippet: Colocalization analysis was carried out by the Linescan tool (Metamorph Premier 7.6 software), and the Image J plugins JaCop, Colocalization colormap and Colocalization threshold.

    Techniques: Immunofluorescence