phenylindole Search Results


93
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Santa Cruz Biotechnology 1 methyl 2 phenylindole
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Santa Cruz Biotechnology immunofluorescence detected dystrophin
Figure 1. Morphometric and myonuclei counting analyses after one and two weeks of electrical stimulation are depicted. (A,B) are representative photomicrographs of <t>dystrophin</t> (green) im- munofluorescence (DAPI in blue, used to identify nuclei) in TA muscle after one and two weeks of electrical stimulation, respectively (50 µm scale bar). (C) Mean fiber cross-sectional area of the TA muscle following one and two weeks of electrical stimulation (n = 5). (D) Distribution of fiber cross-sectional area after one and two weeks of electrical stimulation (n = 5). (E) TA muscle mass analysis after one and two weeks of electrical stimulation (n = 5). (F) Quantity of myonuclei per fiber following electrical stimulation for one and two weeks. (G) Percentage of fibers containing centralized nuclei following electrical stimulation for one and two weeks. The data were displayed as mean ± SEM. Two-way ANOVA was followed by Tukey’s post-test in the statistical analysis. Three independent experiments were conducted. * p < 0.05 versus control and # p < 0.05 versus ES1.
Immunofluorescence Detected Dystrophin, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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MedChemExpress nuclei
Figure 1. Morphometric and myonuclei counting analyses after one and two weeks of electrical stimulation are depicted. (A,B) are representative photomicrographs of <t>dystrophin</t> (green) im- munofluorescence (DAPI in blue, used to identify nuclei) in TA muscle after one and two weeks of electrical stimulation, respectively (50 µm scale bar). (C) Mean fiber cross-sectional area of the TA muscle following one and two weeks of electrical stimulation (n = 5). (D) Distribution of fiber cross-sectional area after one and two weeks of electrical stimulation (n = 5). (E) TA muscle mass analysis after one and two weeks of electrical stimulation (n = 5). (F) Quantity of myonuclei per fiber following electrical stimulation for one and two weeks. (G) Percentage of fibers containing centralized nuclei following electrical stimulation for one and two weeks. The data were displayed as mean ± SEM. Two-way ANOVA was followed by Tukey’s post-test in the statistical analysis. Three independent experiments were conducted. * p < 0.05 versus control and # p < 0.05 versus ES1.
Nuclei, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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MedChemExpress hy d0814
Figure 1. Morphometric and myonuclei counting analyses after one and two weeks of electrical stimulation are depicted. (A,B) are representative photomicrographs of <t>dystrophin</t> (green) im- munofluorescence (DAPI in blue, used to identify nuclei) in TA muscle after one and two weeks of electrical stimulation, respectively (50 µm scale bar). (C) Mean fiber cross-sectional area of the TA muscle following one and two weeks of electrical stimulation (n = 5). (D) Distribution of fiber cross-sectional area after one and two weeks of electrical stimulation (n = 5). (E) TA muscle mass analysis after one and two weeks of electrical stimulation (n = 5). (F) Quantity of myonuclei per fiber following electrical stimulation for one and two weeks. (G) Percentage of fibers containing centralized nuclei following electrical stimulation for one and two weeks. The data were displayed as mean ± SEM. Two-way ANOVA was followed by Tukey’s post-test in the statistical analysis. Three independent experiments were conducted. * p < 0.05 versus control and # p < 0.05 versus ES1.
Hy D0814, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Aladdin Scientific Corporation 4 6 diamidino 2 phenylindole dapi
Figure 1. Morphometric and myonuclei counting analyses after one and two weeks of electrical stimulation are depicted. (A,B) are representative photomicrographs of <t>dystrophin</t> (green) im- munofluorescence (DAPI in blue, used to identify nuclei) in TA muscle after one and two weeks of electrical stimulation, respectively (50 µm scale bar). (C) Mean fiber cross-sectional area of the TA muscle following one and two weeks of electrical stimulation (n = 5). (D) Distribution of fiber cross-sectional area after one and two weeks of electrical stimulation (n = 5). (E) TA muscle mass analysis after one and two weeks of electrical stimulation (n = 5). (F) Quantity of myonuclei per fiber following electrical stimulation for one and two weeks. (G) Percentage of fibers containing centralized nuclei following electrical stimulation for one and two weeks. The data were displayed as mean ± SEM. Two-way ANOVA was followed by Tukey’s post-test in the statistical analysis. Three independent experiments were conducted. * p < 0.05 versus control and # p < 0.05 versus ES1.
4 6 Diamidino 2 Phenylindole Dapi, supplied by Aladdin Scientific Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Boster Bio dapi
Figure 1. Morphometric and myonuclei counting analyses after one and two weeks of electrical stimulation are depicted. (A,B) are representative photomicrographs of <t>dystrophin</t> (green) im- munofluorescence (DAPI in blue, used to identify nuclei) in TA muscle after one and two weeks of electrical stimulation, respectively (50 µm scale bar). (C) Mean fiber cross-sectional area of the TA muscle following one and two weeks of electrical stimulation (n = 5). (D) Distribution of fiber cross-sectional area after one and two weeks of electrical stimulation (n = 5). (E) TA muscle mass analysis after one and two weeks of electrical stimulation (n = 5). (F) Quantity of myonuclei per fiber following electrical stimulation for one and two weeks. (G) Percentage of fibers containing centralized nuclei following electrical stimulation for one and two weeks. The data were displayed as mean ± SEM. Two-way ANOVA was followed by Tukey’s post-test in the statistical analysis. Three independent experiments were conducted. * p < 0.05 versus control and # p < 0.05 versus ES1.
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Thermo Fisher dapi
Figure 1. Morphometric and myonuclei counting analyses after one and two weeks of electrical stimulation are depicted. (A,B) are representative photomicrographs of <t>dystrophin</t> (green) im- munofluorescence (DAPI in blue, used to identify nuclei) in TA muscle after one and two weeks of electrical stimulation, respectively (50 µm scale bar). (C) Mean fiber cross-sectional area of the TA muscle following one and two weeks of electrical stimulation (n = 5). (D) Distribution of fiber cross-sectional area after one and two weeks of electrical stimulation (n = 5). (E) TA muscle mass analysis after one and two weeks of electrical stimulation (n = 5). (F) Quantity of myonuclei per fiber following electrical stimulation for one and two weeks. (G) Percentage of fibers containing centralized nuclei following electrical stimulation for one and two weeks. The data were displayed as mean ± SEM. Two-way ANOVA was followed by Tukey’s post-test in the statistical analysis. Three independent experiments were conducted. * p < 0.05 versus control and # p < 0.05 versus ES1.
Dapi, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Toronto Research Chemicals d416050

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Biosynth Carbosynth 4 6 diamidino 2 phenylindole 2hcl

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Image Search Results


Figure 1. Morphometric and myonuclei counting analyses after one and two weeks of electrical stimulation are depicted. (A,B) are representative photomicrographs of dystrophin (green) im- munofluorescence (DAPI in blue, used to identify nuclei) in TA muscle after one and two weeks of electrical stimulation, respectively (50 µm scale bar). (C) Mean fiber cross-sectional area of the TA muscle following one and two weeks of electrical stimulation (n = 5). (D) Distribution of fiber cross-sectional area after one and two weeks of electrical stimulation (n = 5). (E) TA muscle mass analysis after one and two weeks of electrical stimulation (n = 5). (F) Quantity of myonuclei per fiber following electrical stimulation for one and two weeks. (G) Percentage of fibers containing centralized nuclei following electrical stimulation for one and two weeks. The data were displayed as mean ± SEM. Two-way ANOVA was followed by Tukey’s post-test in the statistical analysis. Three independent experiments were conducted. * p < 0.05 versus control and # p < 0.05 versus ES1.

Journal: Applied Sciences

Article Title: Improved Electrical Stimulation-Based Exercise Model to Induce Mice Tibialis Anterior Muscle Hypertrophy and Function

doi: 10.3390/app12157673

Figure Lengend Snippet: Figure 1. Morphometric and myonuclei counting analyses after one and two weeks of electrical stimulation are depicted. (A,B) are representative photomicrographs of dystrophin (green) im- munofluorescence (DAPI in blue, used to identify nuclei) in TA muscle after one and two weeks of electrical stimulation, respectively (50 µm scale bar). (C) Mean fiber cross-sectional area of the TA muscle following one and two weeks of electrical stimulation (n = 5). (D) Distribution of fiber cross-sectional area after one and two weeks of electrical stimulation (n = 5). (E) TA muscle mass analysis after one and two weeks of electrical stimulation (n = 5). (F) Quantity of myonuclei per fiber following electrical stimulation for one and two weeks. (G) Percentage of fibers containing centralized nuclei following electrical stimulation for one and two weeks. The data were displayed as mean ± SEM. Two-way ANOVA was followed by Tukey’s post-test in the statistical analysis. Three independent experiments were conducted. * p < 0.05 versus control and # p < 0.05 versus ES1.

Article Snippet: Using a cryostat (Leica CM1850 UV, Wetzlar, Germany), samples were transversely sectioned (10-μm-thick), and immunofluorescence detected Dystrophin (Santa Cruz, rabbit anti-Dystrophin #sc-15376, Dallas, TX, USA) and nuclei (through DAPI, 4′,6-diamidino-2phenylindole).

Techniques: Control

Figure 2. Representative immunofluorescence micrographs of IgG-positive (red), dystrophin (green), and DAPI (blue) after one (ES1, n = 5) and two (ES2, n = 5) weeks of electrical stimulation and 4 days after cardiotoxin injection (CTX 4D, n = 4) compared to control (CTR, n = 5). Scale bar: 50 µm.

Journal: Applied Sciences

Article Title: Improved Electrical Stimulation-Based Exercise Model to Induce Mice Tibialis Anterior Muscle Hypertrophy and Function

doi: 10.3390/app12157673

Figure Lengend Snippet: Figure 2. Representative immunofluorescence micrographs of IgG-positive (red), dystrophin (green), and DAPI (blue) after one (ES1, n = 5) and two (ES2, n = 5) weeks of electrical stimulation and 4 days after cardiotoxin injection (CTX 4D, n = 4) compared to control (CTR, n = 5). Scale bar: 50 µm.

Article Snippet: Using a cryostat (Leica CM1850 UV, Wetzlar, Germany), samples were transversely sectioned (10-μm-thick), and immunofluorescence detected Dystrophin (Santa Cruz, rabbit anti-Dystrophin #sc-15376, Dallas, TX, USA) and nuclei (through DAPI, 4′,6-diamidino-2phenylindole).

Techniques: Injection, Control

Journal: STAR Protocols

Article Title: Generation of mixed murine organoids to model cellular interactions

doi: 10.1016/j.xpro.2021.100997

Figure Lengend Snippet:

Article Snippet: 4′,6-Diamidino-2-phenylindole Dihydrochloride (DAPI) , Toronto Research Chemicals , D416050; CAS RN: 28718-90-3.

Techniques: Recombinant, Membrane, Software, Microscopy, Transferring, Polymer