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Functional characterization of HyPer7 as H 2 O 2 sensor in 3 DAG gemmae. (A) Plate reader measurements of HyPer7 fluorescence intensity in 3 DAG gemmae. After 10 min, gemmae were submersed in medium with different H 2 O 2 concentrations (0.25–10 mM) for 10 min, followed by recovery measurements for 100 min. Error bars represent standard deviation, calculated from n ≥ 6. Values were normalized to the 488/405 ratio of the first time point. (B) Microscopic images of HyPer7 fluorescence in 3 DAG transgenic gemmae exposed to the H 2 O 2 series. The rainbow color scheme depicts the detected HyPer7 ratio 488/405 range from low (blue) to high (red) H 2 O 2 <t>concentrations.</t> <t>Ratiometric</t> images visualize spectral changes in response to increasing H 2 O 2 concentrations ( n > 7). Scale bars, overview: 100 μm, insets: 50 μm. Images are maximum intensity Z ‐stack projections processed using <t>RRA</t> software. Insets represent single slice images of corresponding overview Z ‐stack projections. Arrows indicate higher oxidized meristematic zones, disappearing after 2 mM treatments. (C) HyPer7 ratios from the meristematic region (mr) and surrounding differentiated tissue (dt) were determined using representative images ( n = 7) shown in (B). (D) Phenotypic analysis of WT plants after cultivation for 3 days, followed by 10 min H₂O₂ treatment and recovery for 4 days. Plants treated with 10 mM H₂O₂ were non‐viable and excluded from further analysis. Scale bar: 500 μm. (E) Quantitative assessment of the optical surface area of 7‐day‐old WT plants after H₂O₂ treatments ( n > 35). Data are represented as mean ± standard deviation. Statistical significance was determined using the single ANOVA test followed by Tukey ( P < 0.05).
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Functional characterization of HyPer7 as H 2 O 2 sensor in 3 DAG gemmae. (A) Plate reader measurements of HyPer7 fluorescence intensity in 3 DAG gemmae. After 10 min, gemmae were submersed in medium with different H 2 O 2 concentrations (0.25–10 mM) for 10 min, followed by recovery measurements for 100 min. Error bars represent standard deviation, calculated from n ≥ 6. Values were normalized to the 488/405 ratio of the first time point. (B) Microscopic images of HyPer7 fluorescence in 3 DAG transgenic gemmae exposed to the H 2 O 2 series. The rainbow color scheme depicts the detected HyPer7 ratio 488/405 range from low (blue) to high (red) H 2 O 2 <t>concentrations.</t> <t>Ratiometric</t> images visualize spectral changes in response to increasing H 2 O 2 concentrations ( n > 7). Scale bars, overview: 100 μm, insets: 50 μm. Images are maximum intensity Z ‐stack projections processed using <t>RRA</t> software. Insets represent single slice images of corresponding overview Z ‐stack projections. Arrows indicate higher oxidized meristematic zones, disappearing after 2 mM treatments. (C) HyPer7 ratios from the meristematic region (mr) and surrounding differentiated tissue (dt) were determined using representative images ( n = 7) shown in (B). (D) Phenotypic analysis of WT plants after cultivation for 3 days, followed by 10 min H₂O₂ treatment and recovery for 4 days. Plants treated with 10 mM H₂O₂ were non‐viable and excluded from further analysis. Scale bar: 500 μm. (E) Quantitative assessment of the optical surface area of 7‐day‐old WT plants after H₂O₂ treatments ( n > 35). Data are represented as mean ± standard deviation. Statistical significance was determined using the single ANOVA test followed by Tukey ( P < 0.05).
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Functional characterization of HyPer7 as H 2 O 2 sensor in 3 DAG gemmae. (A) Plate reader measurements of HyPer7 fluorescence intensity in 3 DAG gemmae. After 10 min, gemmae were submersed in medium with different H 2 O 2 concentrations (0.25–10 mM) for 10 min, followed by recovery measurements for 100 min. Error bars represent standard deviation, calculated from n ≥ 6. Values were normalized to the 488/405 ratio of the first time point. (B) Microscopic images of HyPer7 fluorescence in 3 DAG transgenic gemmae exposed to the H 2 O 2 series. The rainbow color scheme depicts the detected HyPer7 ratio 488/405 range from low (blue) to high (red) H 2 O 2 <t>concentrations.</t> <t>Ratiometric</t> images visualize spectral changes in response to increasing H 2 O 2 concentrations ( n > 7). Scale bars, overview: 100 μm, insets: 50 μm. Images are maximum intensity Z ‐stack projections processed using <t>RRA</t> software. Insets represent single slice images of corresponding overview Z ‐stack projections. Arrows indicate higher oxidized meristematic zones, disappearing after 2 mM treatments. (C) HyPer7 ratios from the meristematic region (mr) and surrounding differentiated tissue (dt) were determined using representative images ( n = 7) shown in (B). (D) Phenotypic analysis of WT plants after cultivation for 3 days, followed by 10 min H₂O₂ treatment and recovery for 4 days. Plants treated with 10 mM H₂O₂ were non‐viable and excluded from further analysis. Scale bar: 500 μm. (E) Quantitative assessment of the optical surface area of 7‐day‐old WT plants after H₂O₂ treatments ( n > 35). Data are represented as mean ± standard deviation. Statistical significance was determined using the single ANOVA test followed by Tukey ( P < 0.05).
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Functional characterization of HyPer7 as H 2 O 2 sensor in 3 DAG gemmae. (A) Plate reader measurements of HyPer7 fluorescence intensity in 3 DAG gemmae. After 10 min, gemmae were submersed in medium with different H 2 O 2 concentrations (0.25–10 mM) for 10 min, followed by recovery measurements for 100 min. Error bars represent standard deviation, calculated from n ≥ 6. Values were normalized to the 488/405 ratio of the first time point. (B) Microscopic images of HyPer7 fluorescence in 3 DAG transgenic gemmae exposed to the H 2 O 2 series. The rainbow color scheme depicts the detected HyPer7 ratio 488/405 range from low (blue) to high (red) H 2 O 2 <t>concentrations.</t> <t>Ratiometric</t> images visualize spectral changes in response to increasing H 2 O 2 concentrations ( n > 7). Scale bars, overview: 100 μm, insets: 50 μm. Images are maximum intensity Z ‐stack projections processed using <t>RRA</t> software. Insets represent single slice images of corresponding overview Z ‐stack projections. Arrows indicate higher oxidized meristematic zones, disappearing after 2 mM treatments. (C) HyPer7 ratios from the meristematic region (mr) and surrounding differentiated tissue (dt) were determined using representative images ( n = 7) shown in (B). (D) Phenotypic analysis of WT plants after cultivation for 3 days, followed by 10 min H₂O₂ treatment and recovery for 4 days. Plants treated with 10 mM H₂O₂ were non‐viable and excluded from further analysis. Scale bar: 500 μm. (E) Quantitative assessment of the optical surface area of 7‐day‐old WT plants after H₂O₂ treatments ( n > 35). Data are represented as mean ± standard deviation. Statistical significance was determined using the single ANOVA test followed by Tukey ( P < 0.05).
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Functional characterization of HyPer7 as H 2 O 2 sensor in 3 DAG gemmae. (A) Plate reader measurements of HyPer7 fluorescence intensity in 3 DAG gemmae. After 10 min, gemmae were submersed in medium with different H 2 O 2 concentrations (0.25–10 mM) for 10 min, followed by recovery measurements for 100 min. Error bars represent standard deviation, calculated from n ≥ 6. Values were normalized to the 488/405 ratio of the first time point. (B) Microscopic images of HyPer7 fluorescence in 3 DAG transgenic gemmae exposed to the H 2 O 2 series. The rainbow color scheme depicts the detected HyPer7 ratio 488/405 range from low (blue) to high (red) H 2 O 2 <t>concentrations.</t> <t>Ratiometric</t> images visualize spectral changes in response to increasing H 2 O 2 concentrations ( n > 7). Scale bars, overview: 100 μm, insets: 50 μm. Images are maximum intensity Z ‐stack projections processed using <t>RRA</t> software. Insets represent single slice images of corresponding overview Z ‐stack projections. Arrows indicate higher oxidized meristematic zones, disappearing after 2 mM treatments. (C) HyPer7 ratios from the meristematic region (mr) and surrounding differentiated tissue (dt) were determined using representative images ( n = 7) shown in (B). (D) Phenotypic analysis of WT plants after cultivation for 3 days, followed by 10 min H₂O₂ treatment and recovery for 4 days. Plants treated with 10 mM H₂O₂ were non‐viable and excluded from further analysis. Scale bar: 500 μm. (E) Quantitative assessment of the optical surface area of 7‐day‐old WT plants after H₂O₂ treatments ( n > 35). Data are represented as mean ± standard deviation. Statistical significance was determined using the single ANOVA test followed by Tukey ( P < 0.05).
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Functional characterization of HyPer7 as H 2 O 2 sensor in 3 DAG gemmae. (A) Plate reader measurements of HyPer7 fluorescence intensity in 3 DAG gemmae. After 10 min, gemmae were submersed in medium with different H 2 O 2 concentrations (0.25–10 mM) for 10 min, followed by recovery measurements for 100 min. Error bars represent standard deviation, calculated from n ≥ 6. Values were normalized to the 488/405 ratio of the first time point. (B) Microscopic images of HyPer7 fluorescence in 3 DAG transgenic gemmae exposed to the H 2 O 2 series. The rainbow color scheme depicts the detected HyPer7 ratio 488/405 range from low (blue) to high (red) H 2 O 2 <t>concentrations.</t> <t>Ratiometric</t> images visualize spectral changes in response to increasing H 2 O 2 concentrations ( n > 7). Scale bars, overview: 100 μm, insets: 50 μm. Images are maximum intensity Z ‐stack projections processed using <t>RRA</t> software. Insets represent single slice images of corresponding overview Z ‐stack projections. Arrows indicate higher oxidized meristematic zones, disappearing after 2 mM treatments. (C) HyPer7 ratios from the meristematic region (mr) and surrounding differentiated tissue (dt) were determined using representative images ( n = 7) shown in (B). (D) Phenotypic analysis of WT plants after cultivation for 3 days, followed by 10 min H₂O₂ treatment and recovery for 4 days. Plants treated with 10 mM H₂O₂ were non‐viable and excluded from further analysis. Scale bar: 500 μm. (E) Quantitative assessment of the optical surface area of 7‐day‐old WT plants after H₂O₂ treatments ( n > 35). Data are represented as mean ± standard deviation. Statistical significance was determined using the single ANOVA test followed by Tukey ( P < 0.05).
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Functional characterization of HyPer7 as H 2 O 2 sensor in 3 DAG gemmae. (A) Plate reader measurements of HyPer7 fluorescence intensity in 3 DAG gemmae. After 10 min, gemmae were submersed in medium with different H 2 O 2 concentrations (0.25–10 mM) for 10 min, followed by recovery measurements for 100 min. Error bars represent standard deviation, calculated from n ≥ 6. Values were normalized to the 488/405 ratio of the first time point. (B) Microscopic images of HyPer7 fluorescence in 3 DAG transgenic gemmae exposed to the H 2 O 2 series. The rainbow color scheme depicts the detected HyPer7 ratio 488/405 range from low (blue) to high (red) H 2 O 2 <t>concentrations.</t> <t>Ratiometric</t> images visualize spectral changes in response to increasing H 2 O 2 concentrations ( n > 7). Scale bars, overview: 100 μm, insets: 50 μm. Images are maximum intensity Z ‐stack projections processed using <t>RRA</t> software. Insets represent single slice images of corresponding overview Z ‐stack projections. Arrows indicate higher oxidized meristematic zones, disappearing after 2 mM treatments. (C) HyPer7 ratios from the meristematic region (mr) and surrounding differentiated tissue (dt) were determined using representative images ( n = 7) shown in (B). (D) Phenotypic analysis of WT plants after cultivation for 3 days, followed by 10 min H₂O₂ treatment and recovery for 4 days. Plants treated with 10 mM H₂O₂ were non‐viable and excluded from further analysis. Scale bar: 500 μm. (E) Quantitative assessment of the optical surface area of 7‐day‐old WT plants after H₂O₂ treatments ( n > 35). Data are represented as mean ± standard deviation. Statistical significance was determined using the single ANOVA test followed by Tukey ( P < 0.05).
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Image Search Results


Functional characterization of HyPer7 as H 2 O 2 sensor in 3 DAG gemmae. (A) Plate reader measurements of HyPer7 fluorescence intensity in 3 DAG gemmae. After 10 min, gemmae were submersed in medium with different H 2 O 2 concentrations (0.25–10 mM) for 10 min, followed by recovery measurements for 100 min. Error bars represent standard deviation, calculated from n ≥ 6. Values were normalized to the 488/405 ratio of the first time point. (B) Microscopic images of HyPer7 fluorescence in 3 DAG transgenic gemmae exposed to the H 2 O 2 series. The rainbow color scheme depicts the detected HyPer7 ratio 488/405 range from low (blue) to high (red) H 2 O 2 concentrations. Ratiometric images visualize spectral changes in response to increasing H 2 O 2 concentrations ( n > 7). Scale bars, overview: 100 μm, insets: 50 μm. Images are maximum intensity Z ‐stack projections processed using RRA software. Insets represent single slice images of corresponding overview Z ‐stack projections. Arrows indicate higher oxidized meristematic zones, disappearing after 2 mM treatments. (C) HyPer7 ratios from the meristematic region (mr) and surrounding differentiated tissue (dt) were determined using representative images ( n = 7) shown in (B). (D) Phenotypic analysis of WT plants after cultivation for 3 days, followed by 10 min H₂O₂ treatment and recovery for 4 days. Plants treated with 10 mM H₂O₂ were non‐viable and excluded from further analysis. Scale bar: 500 μm. (E) Quantitative assessment of the optical surface area of 7‐day‐old WT plants after H₂O₂ treatments ( n > 35). Data are represented as mean ± standard deviation. Statistical significance was determined using the single ANOVA test followed by Tukey ( P < 0.05).

Journal: The Plant Journal

Article Title: Redox buffering and H 2 O 2 orchestrate the vegetative development of Marchantia polymorpha

doi: 10.1111/tpj.70317

Figure Lengend Snippet: Functional characterization of HyPer7 as H 2 O 2 sensor in 3 DAG gemmae. (A) Plate reader measurements of HyPer7 fluorescence intensity in 3 DAG gemmae. After 10 min, gemmae were submersed in medium with different H 2 O 2 concentrations (0.25–10 mM) for 10 min, followed by recovery measurements for 100 min. Error bars represent standard deviation, calculated from n ≥ 6. Values were normalized to the 488/405 ratio of the first time point. (B) Microscopic images of HyPer7 fluorescence in 3 DAG transgenic gemmae exposed to the H 2 O 2 series. The rainbow color scheme depicts the detected HyPer7 ratio 488/405 range from low (blue) to high (red) H 2 O 2 concentrations. Ratiometric images visualize spectral changes in response to increasing H 2 O 2 concentrations ( n > 7). Scale bars, overview: 100 μm, insets: 50 μm. Images are maximum intensity Z ‐stack projections processed using RRA software. Insets represent single slice images of corresponding overview Z ‐stack projections. Arrows indicate higher oxidized meristematic zones, disappearing after 2 mM treatments. (C) HyPer7 ratios from the meristematic region (mr) and surrounding differentiated tissue (dt) were determined using representative images ( n = 7) shown in (B). (D) Phenotypic analysis of WT plants after cultivation for 3 days, followed by 10 min H₂O₂ treatment and recovery for 4 days. Plants treated with 10 mM H₂O₂ were non‐viable and excluded from further analysis. Scale bar: 500 μm. (E) Quantitative assessment of the optical surface area of 7‐day‐old WT plants after H₂O₂ treatments ( n > 35). Data are represented as mean ± standard deviation. Statistical significance was determined using the single ANOVA test followed by Tukey ( P < 0.05).

Article Snippet: A ratiometric analysis was performed by calculating the 405/488 nm ratio for each pixel using the Matlab‐based program Redox Ratio Analysis (RRA), resulting in a false color ratiometric image according to Fricker ( ).

Techniques: Functional Assay, Fluorescence, Standard Deviation, Transgenic Assay, Software

Techniques for Better Visualization of PVS

Journal: Journal of the Korean Society of Radiology (Taehan Yŏngsang Ŭihakhoe chi)

Article Title: 늘어난 혈관주위공간: 노화와 신경계질환에서의 임상적의의와 영상의 역할

doi: 10.3348/jksr.2022.0049

Figure Lengend Snippet: Techniques for Better Visualization of PVS

Article Snippet: Niazi et al. ( ) , Automated segmentation using MATLAB Pixel-based mapping with volume calculation , NC; 15 MCI; 14 , 3T T2WI , WM and BG area , Quantification result VF of EPVS control vs. aMCI 2.82_0.40 v/v% vs. 4.17_0.57 v/v% The threshold value that achieves the best compromise between sensitivity (92.86%) and specificity (93.33%) is 3.35 v/v%.

Techniques: Control, Imaging