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linear mvrg  (MathWorks Inc)


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    Structured Review

    MathWorks Inc linear mvrg
    Coefficients from <t>MVRG</t> of (A) SM diffusion coefficient on local speckle density and displacement magnitude, and (B) SM intensity on local speckle density, displacement magnitude and intensity for CD36 (magenta), TM-ABD (yellow) and TM-ABD* (blue). MVRG analysis was performed separately for the four indicated subgroups of SM tracklets based on diffusion type and local speckle density pairings. Colors, circles, red lines and shaded bars as in and . MVRG coefficients significantly different from zero (dashed grey line), tested by t-test, are indicated by *, **, *** above the MVRG coefficient plots for p-value ≤ 0.05, 0.01, 0.001, respectively. Differences between the MVRG coefficients of different PM proteins, tested by ANOVA followed by Tukey-Kramer post-hoc analysis, are indicated by * above bracket for p-value ≤ 0.05. Inset pictograms: visual summary of MVRG results. Triangle slope and direction represent significance and sign (positive or negative) of MVRG coefficient; rectangles indicate not significant MVRG coefficients. Next to the triangles, +, ++, +++ (and corresponding −, −−, −−−) indicate significant differences between free and confined MVRG coefficients at the same density level (e.g., sparse free vs. sparse confined) for each PM protein, tested by paired t-test, for p-value ≤ 0.05, 0.01, 0.001, respectively. In all tests, p-values > 0.05 are not explicitly indicated. See for sample size and other dataset details.
    Linear Mvrg, supplied by MathWorks 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/linear mvrg/product/MathWorks Inc
    Average 90 stars, based on 1 article reviews
    linear mvrg - by Bioz Stars, 2026-04
    90/100 stars

    Images

    1) Product Images from "Multiscale imaging and quantitative analysis of plasma membrane protein-cortical actin interplay"

    Article Title: Multiscale imaging and quantitative analysis of plasma membrane protein-cortical actin interplay

    Journal: bioRxiv

    doi: 10.1101/2023.01.22.525112

    Coefficients from MVRG of (A) SM diffusion coefficient on local speckle density and displacement magnitude, and (B) SM intensity on local speckle density, displacement magnitude and intensity for CD36 (magenta), TM-ABD (yellow) and TM-ABD* (blue). MVRG analysis was performed separately for the four indicated subgroups of SM tracklets based on diffusion type and local speckle density pairings. Colors, circles, red lines and shaded bars as in and . MVRG coefficients significantly different from zero (dashed grey line), tested by t-test, are indicated by *, **, *** above the MVRG coefficient plots for p-value ≤ 0.05, 0.01, 0.001, respectively. Differences between the MVRG coefficients of different PM proteins, tested by ANOVA followed by Tukey-Kramer post-hoc analysis, are indicated by * above bracket for p-value ≤ 0.05. Inset pictograms: visual summary of MVRG results. Triangle slope and direction represent significance and sign (positive or negative) of MVRG coefficient; rectangles indicate not significant MVRG coefficients. Next to the triangles, +, ++, +++ (and corresponding −, −−, −−−) indicate significant differences between free and confined MVRG coefficients at the same density level (e.g., sparse free vs. sparse confined) for each PM protein, tested by paired t-test, for p-value ≤ 0.05, 0.01, 0.001, respectively. In all tests, p-values > 0.05 are not explicitly indicated. See for sample size and other dataset details.
    Figure Legend Snippet: Coefficients from MVRG of (A) SM diffusion coefficient on local speckle density and displacement magnitude, and (B) SM intensity on local speckle density, displacement magnitude and intensity for CD36 (magenta), TM-ABD (yellow) and TM-ABD* (blue). MVRG analysis was performed separately for the four indicated subgroups of SM tracklets based on diffusion type and local speckle density pairings. Colors, circles, red lines and shaded bars as in and . MVRG coefficients significantly different from zero (dashed grey line), tested by t-test, are indicated by *, **, *** above the MVRG coefficient plots for p-value ≤ 0.05, 0.01, 0.001, respectively. Differences between the MVRG coefficients of different PM proteins, tested by ANOVA followed by Tukey-Kramer post-hoc analysis, are indicated by * above bracket for p-value ≤ 0.05. Inset pictograms: visual summary of MVRG results. Triangle slope and direction represent significance and sign (positive or negative) of MVRG coefficient; rectangles indicate not significant MVRG coefficients. Next to the triangles, +, ++, +++ (and corresponding −, −−, −−−) indicate significant differences between free and confined MVRG coefficients at the same density level (e.g., sparse free vs. sparse confined) for each PM protein, tested by paired t-test, for p-value ≤ 0.05, 0.01, 0.001, respectively. In all tests, p-values > 0.05 are not explicitly indicated. See for sample size and other dataset details.

    Techniques Used: Diffusion-based Assay



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    MathWorks Inc linear mvrg
    Coefficients from <t>MVRG</t> of (A) SM diffusion coefficient on local speckle density and displacement magnitude, and (B) SM intensity on local speckle density, displacement magnitude and intensity for CD36 (magenta), TM-ABD (yellow) and TM-ABD* (blue). MVRG analysis was performed separately for the four indicated subgroups of SM tracklets based on diffusion type and local speckle density pairings. Colors, circles, red lines and shaded bars as in and . MVRG coefficients significantly different from zero (dashed grey line), tested by t-test, are indicated by *, **, *** above the MVRG coefficient plots for p-value ≤ 0.05, 0.01, 0.001, respectively. Differences between the MVRG coefficients of different PM proteins, tested by ANOVA followed by Tukey-Kramer post-hoc analysis, are indicated by * above bracket for p-value ≤ 0.05. Inset pictograms: visual summary of MVRG results. Triangle slope and direction represent significance and sign (positive or negative) of MVRG coefficient; rectangles indicate not significant MVRG coefficients. Next to the triangles, +, ++, +++ (and corresponding −, −−, −−−) indicate significant differences between free and confined MVRG coefficients at the same density level (e.g., sparse free vs. sparse confined) for each PM protein, tested by paired t-test, for p-value ≤ 0.05, 0.01, 0.001, respectively. In all tests, p-values > 0.05 are not explicitly indicated. See for sample size and other dataset details.
    Linear Mvrg, supplied by MathWorks 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/linear mvrg/product/MathWorks Inc
    Average 90 stars, based on 1 article reviews
    linear mvrg - by Bioz Stars, 2026-04
    90/100 stars
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    Coefficients from MVRG of (A) SM diffusion coefficient on local speckle density and displacement magnitude, and (B) SM intensity on local speckle density, displacement magnitude and intensity for CD36 (magenta), TM-ABD (yellow) and TM-ABD* (blue). MVRG analysis was performed separately for the four indicated subgroups of SM tracklets based on diffusion type and local speckle density pairings. Colors, circles, red lines and shaded bars as in and . MVRG coefficients significantly different from zero (dashed grey line), tested by t-test, are indicated by *, **, *** above the MVRG coefficient plots for p-value ≤ 0.05, 0.01, 0.001, respectively. Differences between the MVRG coefficients of different PM proteins, tested by ANOVA followed by Tukey-Kramer post-hoc analysis, are indicated by * above bracket for p-value ≤ 0.05. Inset pictograms: visual summary of MVRG results. Triangle slope and direction represent significance and sign (positive or negative) of MVRG coefficient; rectangles indicate not significant MVRG coefficients. Next to the triangles, +, ++, +++ (and corresponding −, −−, −−−) indicate significant differences between free and confined MVRG coefficients at the same density level (e.g., sparse free vs. sparse confined) for each PM protein, tested by paired t-test, for p-value ≤ 0.05, 0.01, 0.001, respectively. In all tests, p-values > 0.05 are not explicitly indicated. See for sample size and other dataset details.

    Journal: bioRxiv

    Article Title: Multiscale imaging and quantitative analysis of plasma membrane protein-cortical actin interplay

    doi: 10.1101/2023.01.22.525112

    Figure Lengend Snippet: Coefficients from MVRG of (A) SM diffusion coefficient on local speckle density and displacement magnitude, and (B) SM intensity on local speckle density, displacement magnitude and intensity for CD36 (magenta), TM-ABD (yellow) and TM-ABD* (blue). MVRG analysis was performed separately for the four indicated subgroups of SM tracklets based on diffusion type and local speckle density pairings. Colors, circles, red lines and shaded bars as in and . MVRG coefficients significantly different from zero (dashed grey line), tested by t-test, are indicated by *, **, *** above the MVRG coefficient plots for p-value ≤ 0.05, 0.01, 0.001, respectively. Differences between the MVRG coefficients of different PM proteins, tested by ANOVA followed by Tukey-Kramer post-hoc analysis, are indicated by * above bracket for p-value ≤ 0.05. Inset pictograms: visual summary of MVRG results. Triangle slope and direction represent significance and sign (positive or negative) of MVRG coefficient; rectangles indicate not significant MVRG coefficients. Next to the triangles, +, ++, +++ (and corresponding −, −−, −−−) indicate significant differences between free and confined MVRG coefficients at the same density level (e.g., sparse free vs. sparse confined) for each PM protein, tested by paired t-test, for p-value ≤ 0.05, 0.01, 0.001, respectively. In all tests, p-values > 0.05 are not explicitly indicated. See for sample size and other dataset details.

    Article Snippet: Linear MVRG (using the MATLAB function mvregress()) was performed on an individual cell (movie) basis.

    Techniques: Diffusion-based Assay