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traction force microscopy data analysis  (GraphPad Software Inc)


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    Structured Review

    GraphPad Software Inc traction force microscopy data analysis
    R491 increases the fraction and number of small focal adhesions. (A) Representative confocal <t>microscopy</t> images of BJ-Ras cells treated with 5 μM control or R491, showing vimentin, phospho-tyrosine, F-actin, as indicated, and merged images with vimentin (red), phospho-tyrosine (yellow), actin (green) and nuclei (blue). Inset images: magnified views of boxed areas in the larger images. Scale bars: 10 μm. The graphs show (B) the average size of cell-matrix adhesions/per cell, with n = 516 and 478 focal adhesions for control- and R491-treated cells, respectively, and (C) the frequency distribution of the binned sizes of focal adhesions of control- (black) or R491- (grey) treated cells. ** p ≤ 0.01. The difference in the frequency distribution was significant with p ≤ 0.0001.
    Traction Force Microscopy Data Analysis, supplied by GraphPad Software 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/result/traction force microscopy data analysis/product/GraphPad Software Inc
    Average 90 stars, based on 1 article reviews
    traction force microscopy data analysis - by Bioz Stars, 2026-06
    90/100 stars

    Images

    1) Product Images from "ALD-R491 regulates vimentin filament stability and solubility, cell contractile force, cell migration speed and directionality"

    Article Title: ALD-R491 regulates vimentin filament stability and solubility, cell contractile force, cell migration speed and directionality

    Journal: Frontiers in Cell and Developmental Biology

    doi: 10.3389/fcell.2022.926283

    R491 increases the fraction and number of small focal adhesions. (A) Representative confocal microscopy images of BJ-Ras cells treated with 5 μM control or R491, showing vimentin, phospho-tyrosine, F-actin, as indicated, and merged images with vimentin (red), phospho-tyrosine (yellow), actin (green) and nuclei (blue). Inset images: magnified views of boxed areas in the larger images. Scale bars: 10 μm. The graphs show (B) the average size of cell-matrix adhesions/per cell, with n = 516 and 478 focal adhesions for control- and R491-treated cells, respectively, and (C) the frequency distribution of the binned sizes of focal adhesions of control- (black) or R491- (grey) treated cells. ** p ≤ 0.01. The difference in the frequency distribution was significant with p ≤ 0.0001.
    Figure Legend Snippet: R491 increases the fraction and number of small focal adhesions. (A) Representative confocal microscopy images of BJ-Ras cells treated with 5 μM control or R491, showing vimentin, phospho-tyrosine, F-actin, as indicated, and merged images with vimentin (red), phospho-tyrosine (yellow), actin (green) and nuclei (blue). Inset images: magnified views of boxed areas in the larger images. Scale bars: 10 μm. The graphs show (B) the average size of cell-matrix adhesions/per cell, with n = 516 and 478 focal adhesions for control- and R491-treated cells, respectively, and (C) the frequency distribution of the binned sizes of focal adhesions of control- (black) or R491- (grey) treated cells. ** p ≤ 0.01. The difference in the frequency distribution was significant with p ≤ 0.0001.

    Techniques Used: Confocal Microscopy, Control



    Similar Products

    traction force microscopy data analysis  (GraphPad Software Inc)
    90
    GraphPad Software Inc traction force microscopy data analysis
    R491 increases the fraction and number of small focal adhesions. (A) Representative confocal <t>microscopy</t> images of BJ-Ras cells treated with 5 μM control or R491, showing vimentin, phospho-tyrosine, F-actin, as indicated, and merged images with vimentin (red), phospho-tyrosine (yellow), actin (green) and nuclei (blue). Inset images: magnified views of boxed areas in the larger images. Scale bars: 10 μm. The graphs show (B) the average size of cell-matrix adhesions/per cell, with n = 516 and 478 focal adhesions for control- and R491-treated cells, respectively, and (C) the frequency distribution of the binned sizes of focal adhesions of control- (black) or R491- (grey) treated cells. ** p ≤ 0.01. The difference in the frequency distribution was significant with p ≤ 0.0001.
    Traction Force Microscopy Data Analysis, supplied by GraphPad Software 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/result/traction force microscopy data analysis/product/GraphPad Software Inc
    Average 90 stars, based on 1 article reviews
    traction force microscopy data analysis - by Bioz Stars, 2026-06
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    R491 increases the fraction and number of small focal adhesions. (A) Representative confocal microscopy images of BJ-Ras cells treated with 5 μM control or R491, showing vimentin, phospho-tyrosine, F-actin, as indicated, and merged images with vimentin (red), phospho-tyrosine (yellow), actin (green) and nuclei (blue). Inset images: magnified views of boxed areas in the larger images. Scale bars: 10 μm. The graphs show (B) the average size of cell-matrix adhesions/per cell, with n = 516 and 478 focal adhesions for control- and R491-treated cells, respectively, and (C) the frequency distribution of the binned sizes of focal adhesions of control- (black) or R491- (grey) treated cells. ** p ≤ 0.01. The difference in the frequency distribution was significant with p ≤ 0.0001.

    Journal: Frontiers in Cell and Developmental Biology

    Article Title: ALD-R491 regulates vimentin filament stability and solubility, cell contractile force, cell migration speed and directionality

    doi: 10.3389/fcell.2022.926283

    Figure Lengend Snippet: R491 increases the fraction and number of small focal adhesions. (A) Representative confocal microscopy images of BJ-Ras cells treated with 5 μM control or R491, showing vimentin, phospho-tyrosine, F-actin, as indicated, and merged images with vimentin (red), phospho-tyrosine (yellow), actin (green) and nuclei (blue). Inset images: magnified views of boxed areas in the larger images. Scale bars: 10 μm. The graphs show (B) the average size of cell-matrix adhesions/per cell, with n = 516 and 478 focal adhesions for control- and R491-treated cells, respectively, and (C) the frequency distribution of the binned sizes of focal adhesions of control- (black) or R491- (grey) treated cells. ** p ≤ 0.01. The difference in the frequency distribution was significant with p ≤ 0.0001.

    Article Snippet: The mean values of the aspect ratio, cell migration speed and persistence, cells from which debris is detached and left behind during migration, filament distribution, as well as Traction force microscopy data were analyzed using GraphPad Prism (v.9.3.1).

    Techniques: Confocal Microscopy, Control