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budpolarity matlab program  (MathWorks Inc)


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    MathWorks Inc budpolarity matlab program
    (A and B) Isotropic conditions. Gβ cells and GβP− cells expressing the receptor reporter Ste2-GFP were treated with pheromone at time zero and with LatA after global receptor internalization (15 min). (A) Representative images of the indicated cells to visualize Ste2-GFP. Arrowheads indicate Ste2-GFP crescents. (B) Polarity Indices (PIs) for the cells represented in (A) were measured as described for Fig. 2D. Data are means ± SEM of at least 30 cells of each strain from three experiments. *P < 0.03. (C and D) Mating mixtures. (C) Time-lapse images of mating Gβ cells and GβP− cells showing Ste2-GFP localization. Insets show heat map images analyzed using the <t>BudPolarity</t> Matlab program (61), which quantifies signal intensity along the long axis of the cell. (D) Output BudPolarity trace of the pictured cell (inset). Receptor polarization in the cells represented in (C) was quantified by dividing the peak fluorescence signal at the plasma membrane by the minimum fluorescence at the plasma membrane before morphogenesis became apparent. Mean polarization values ± SEM were 1.76 ± 0.14 and 1.28 ± 0.07 for Gβ cells and GβP− cells, respectively (P < 0.007). Data are means ± SEM of at least 17 cells of each strain from two independent experiments.
    Budpolarity Matlab Program, 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/budpolarity matlab program/product/MathWorks Inc
    Average 90 stars, based on 1 article reviews
    budpolarity matlab program - by Bioz Stars, 2026-03
    90/100 stars

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    1) Product Images from "Gβ promotes pheromone receptor polarization and yeast chemotropism by inhibiting receptor phosphorylation"

    Article Title: Gβ promotes pheromone receptor polarization and yeast chemotropism by inhibiting receptor phosphorylation

    Journal: Science signaling

    doi: 10.1126/scisignal.aad4376

    (A and B) Isotropic conditions. Gβ cells and GβP− cells expressing the receptor reporter Ste2-GFP were treated with pheromone at time zero and with LatA after global receptor internalization (15 min). (A) Representative images of the indicated cells to visualize Ste2-GFP. Arrowheads indicate Ste2-GFP crescents. (B) Polarity Indices (PIs) for the cells represented in (A) were measured as described for Fig. 2D. Data are means ± SEM of at least 30 cells of each strain from three experiments. *P < 0.03. (C and D) Mating mixtures. (C) Time-lapse images of mating Gβ cells and GβP− cells showing Ste2-GFP localization. Insets show heat map images analyzed using the BudPolarity Matlab program (61), which quantifies signal intensity along the long axis of the cell. (D) Output BudPolarity trace of the pictured cell (inset). Receptor polarization in the cells represented in (C) was quantified by dividing the peak fluorescence signal at the plasma membrane by the minimum fluorescence at the plasma membrane before morphogenesis became apparent. Mean polarization values ± SEM were 1.76 ± 0.14 and 1.28 ± 0.07 for Gβ cells and GβP− cells, respectively (P < 0.007). Data are means ± SEM of at least 17 cells of each strain from two independent experiments.
    Figure Legend Snippet: (A and B) Isotropic conditions. Gβ cells and GβP− cells expressing the receptor reporter Ste2-GFP were treated with pheromone at time zero and with LatA after global receptor internalization (15 min). (A) Representative images of the indicated cells to visualize Ste2-GFP. Arrowheads indicate Ste2-GFP crescents. (B) Polarity Indices (PIs) for the cells represented in (A) were measured as described for Fig. 2D. Data are means ± SEM of at least 30 cells of each strain from three experiments. *P < 0.03. (C and D) Mating mixtures. (C) Time-lapse images of mating Gβ cells and GβP− cells showing Ste2-GFP localization. Insets show heat map images analyzed using the BudPolarity Matlab program (61), which quantifies signal intensity along the long axis of the cell. (D) Output BudPolarity trace of the pictured cell (inset). Receptor polarization in the cells represented in (C) was quantified by dividing the peak fluorescence signal at the plasma membrane by the minimum fluorescence at the plasma membrane before morphogenesis became apparent. Mean polarization values ± SEM were 1.76 ± 0.14 and 1.28 ± 0.07 for Gβ cells and GβP− cells, respectively (P < 0.007). Data are means ± SEM of at least 17 cells of each strain from two independent experiments.

    Techniques Used: Expressing, Fluorescence, Clinical Proteomics, Membrane



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    budpolarity matlab program  (MathWorks Inc)
    90
    MathWorks Inc budpolarity matlab program
    (A and B) Isotropic conditions. Gβ cells and GβP− cells expressing the receptor reporter Ste2-GFP were treated with pheromone at time zero and with LatA after global receptor internalization (15 min). (A) Representative images of the indicated cells to visualize Ste2-GFP. Arrowheads indicate Ste2-GFP crescents. (B) Polarity Indices (PIs) for the cells represented in (A) were measured as described for Fig. 2D. Data are means ± SEM of at least 30 cells of each strain from three experiments. *P < 0.03. (C and D) Mating mixtures. (C) Time-lapse images of mating Gβ cells and GβP− cells showing Ste2-GFP localization. Insets show heat map images analyzed using the <t>BudPolarity</t> Matlab program (61), which quantifies signal intensity along the long axis of the cell. (D) Output BudPolarity trace of the pictured cell (inset). Receptor polarization in the cells represented in (C) was quantified by dividing the peak fluorescence signal at the plasma membrane by the minimum fluorescence at the plasma membrane before morphogenesis became apparent. Mean polarization values ± SEM were 1.76 ± 0.14 and 1.28 ± 0.07 for Gβ cells and GβP− cells, respectively (P < 0.007). Data are means ± SEM of at least 17 cells of each strain from two independent experiments.
    Budpolarity Matlab Program, 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/budpolarity matlab program/product/MathWorks Inc
    Average 90 stars, based on 1 article reviews
    budpolarity matlab program - by Bioz Stars, 2026-03
    90/100 stars
    		  Buy from Supplier

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    (A and B) Isotropic conditions. Gβ cells and GβP− cells expressing the receptor reporter Ste2-GFP were treated with pheromone at time zero and with LatA after global receptor internalization (15 min). (A) Representative images of the indicated cells to visualize Ste2-GFP. Arrowheads indicate Ste2-GFP crescents. (B) Polarity Indices (PIs) for the cells represented in (A) were measured as described for Fig. 2D. Data are means ± SEM of at least 30 cells of each strain from three experiments. *P < 0.03. (C and D) Mating mixtures. (C) Time-lapse images of mating Gβ cells and GβP− cells showing Ste2-GFP localization. Insets show heat map images analyzed using the BudPolarity Matlab program (61), which quantifies signal intensity along the long axis of the cell. (D) Output BudPolarity trace of the pictured cell (inset). Receptor polarization in the cells represented in (C) was quantified by dividing the peak fluorescence signal at the plasma membrane by the minimum fluorescence at the plasma membrane before morphogenesis became apparent. Mean polarization values ± SEM were 1.76 ± 0.14 and 1.28 ± 0.07 for Gβ cells and GβP− cells, respectively (P < 0.007). Data are means ± SEM of at least 17 cells of each strain from two independent experiments.

    Journal: Science signaling

    Article Title: Gβ promotes pheromone receptor polarization and yeast chemotropism by inhibiting receptor phosphorylation

    doi: 10.1126/scisignal.aad4376

    Figure Lengend Snippet: (A and B) Isotropic conditions. Gβ cells and GβP− cells expressing the receptor reporter Ste2-GFP were treated with pheromone at time zero and with LatA after global receptor internalization (15 min). (A) Representative images of the indicated cells to visualize Ste2-GFP. Arrowheads indicate Ste2-GFP crescents. (B) Polarity Indices (PIs) for the cells represented in (A) were measured as described for Fig. 2D. Data are means ± SEM of at least 30 cells of each strain from three experiments. *P < 0.03. (C and D) Mating mixtures. (C) Time-lapse images of mating Gβ cells and GβP− cells showing Ste2-GFP localization. Insets show heat map images analyzed using the BudPolarity Matlab program (61), which quantifies signal intensity along the long axis of the cell. (D) Output BudPolarity trace of the pictured cell (inset). Receptor polarization in the cells represented in (C) was quantified by dividing the peak fluorescence signal at the plasma membrane by the minimum fluorescence at the plasma membrane before morphogenesis became apparent. Mean polarization values ± SEM were 1.76 ± 0.14 and 1.28 ± 0.07 for Gβ cells and GβP− cells, respectively (P < 0.007). Data are means ± SEM of at least 17 cells of each strain from two independent experiments.

    Article Snippet: Images were sum-projected with ImageJ and the signal intensity along the long axis of the cell was quantified using the BudPolarity Matlab program ( 61b ).

    Techniques: Expressing, Fluorescence, Clinical Proteomics, Membrane