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gaussian multipeaks fit  (OriginLab corp)


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    OriginLab corp gaussian multipeaks fit
    Gaussian Multipeaks Fit, supplied by OriginLab corp, 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/multipeak+gaussian/gaussian+peak+fitting/pm39747172-99-5-17
    Average 90 stars, based on 1 article reviews
    gaussian multipeaks fit - by Bioz Stars, 2026-10
    90/100 stars

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    other:

    Article Title: High-speed single-molecule imaging reveals signal transduction by induced transbilayer raft phases
    Article Snippet: Histograms were fitted with a multipeak Gaussian by using Origin5 (OriginLab Corp.).



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    Figure 4. Pressure-induced membrane stretch activates TMEM16A channels in arterial smooth muscle cells. A, Reduction in pipette pressure from 0 to −40 mm Hg stimulates inward currents that are partially inhibited by the TMEM16 A-inhibitory antibody. Traces represent the average of current recordings of 29 control and 18 TMEM16A antibody-exposed patches at −80 mV. B, Exemplary recordings of single channels activated by −40 mm Hg pressure and inhibited by the TMEM16A-inhibitory antibody. C, All-points histograms of arterial smooth muscle cell patches fit with a <t>gaussian</t> function for −40 mm Hg pressure in the absence and presence of the TMEM16A antibody. D, Original cell-attached recordings of recombinant TMEM16A channels expressed in HEK293 cells in the absence and presence of the TMEM16A inhibitory antibody. No patch pressure was applied during experiments on HEK293 cells. E, All-points histograms of recombinant TMEM16A channels fit with a gaussian function in the absence and presence of the TMEM16A antibody.
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    Image Search Results


    Statistical analysis of β-gal populations. (A) Histogram of β-gal activities. T1∼T4 labels indicate the number of active monomers in the expressed β-gal. Dashed lines with different colors represent multipeak Gaussian fitting using OriginPro software (Origin Lab): T1, black; T2, red; T3, blue; and T4, pink. Turnover rates of enzymes are calculated by comparing the raw intensity changes with a resorufin calibration curve (SI Appendix, Fig. S8). (B) Peak positions. The peak positions are acquired through Gaussian fitting of the activity histogram in A.

    Journal: Proceedings of the National Academy of Sciences of the United States of America

    Article Title: Bottom-up single-molecule strategy for understanding subunit function of tetrameric β-galactosidase

    doi: 10.1073/pnas.1805690115

    Figure Lengend Snippet: Statistical analysis of β-gal populations. (A) Histogram of β-gal activities. T1∼T4 labels indicate the number of active monomers in the expressed β-gal. Dashed lines with different colors represent multipeak Gaussian fitting using OriginPro software (Origin Lab): T1, black; T2, red; T3, blue; and T4, pink. Turnover rates of enzymes are calculated by comparing the raw intensity changes with a resorufin calibration curve (SI Appendix, Fig. S8). (B) Peak positions. The peak positions are acquired through Gaussian fitting of the activity histogram in A.

    Article Snippet: Dashed lines with different colors represent multipeak Gaussian fitting using OriginPro software (Origin Lab): T1, black; T2, red; T3, blue; and T4, pink.

    Techniques: Software, Activity Assay

    Figure 4. Pressure-induced membrane stretch activates TMEM16A channels in arterial smooth muscle cells. A, Reduction in pipette pressure from 0 to −40 mm Hg stimulates inward currents that are partially inhibited by the TMEM16 A-inhibitory antibody. Traces represent the average of current recordings of 29 control and 18 TMEM16A antibody-exposed patches at −80 mV. B, Exemplary recordings of single channels activated by −40 mm Hg pressure and inhibited by the TMEM16A-inhibitory antibody. C, All-points histograms of arterial smooth muscle cell patches fit with a gaussian function for −40 mm Hg pressure in the absence and presence of the TMEM16A antibody. D, Original cell-attached recordings of recombinant TMEM16A channels expressed in HEK293 cells in the absence and presence of the TMEM16A inhibitory antibody. No patch pressure was applied during experiments on HEK293 cells. E, All-points histograms of recombinant TMEM16A channels fit with a gaussian function in the absence and presence of the TMEM16A antibody.

    Journal: Circulation Research

    Article Title: TMEM16A/ANO1 Channels Contribute to the Myogenic Response in Cerebral Arteries

    doi: 10.1161/circresaha.112.277145

    Figure Lengend Snippet: Figure 4. Pressure-induced membrane stretch activates TMEM16A channels in arterial smooth muscle cells. A, Reduction in pipette pressure from 0 to −40 mm Hg stimulates inward currents that are partially inhibited by the TMEM16 A-inhibitory antibody. Traces represent the average of current recordings of 29 control and 18 TMEM16A antibody-exposed patches at −80 mV. B, Exemplary recordings of single channels activated by −40 mm Hg pressure and inhibited by the TMEM16A-inhibitory antibody. C, All-points histograms of arterial smooth muscle cell patches fit with a gaussian function for −40 mm Hg pressure in the absence and presence of the TMEM16A antibody. D, Original cell-attached recordings of recombinant TMEM16A channels expressed in HEK293 cells in the absence and presence of the TMEM16A inhibitory antibody. No patch pressure was applied during experiments on HEK293 cells. E, All-points histograms of recombinant TMEM16A channels fit with a gaussian function in the absence and presence of the TMEM16A antibody.

    Article Snippet: All- points histograms were fit with a multipeak gaussian function, using Microcal Origin.

    Techniques: Membrane, Transferring, Control, Recombinant