microscopy data Search Results


oim analysis 7 2 0  (Gatan Inc)
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scanning tunneling microscopy/spectroscopy (sts/stm) data  (Verlag GmbH)
90
Verlag GmbH scanning tunneling microscopy/spectroscopy (sts/stm) data
Scanning Tunneling Microscopy/Spectroscopy (Sts/Stm) Data, supplied by Verlag GmbH, 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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microscopy data  (MetaMorph Inc)
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interference reflection microscopy (irm) data  (GraphPad Software Inc)
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GraphPad Software Inc interference reflection microscopy (irm) data
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optical microscopy image data  (UES Inc)
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traction force microscopy data analysis  (GraphPad Software Inc)
90
GraphPad Software Inc traction force microscopy data analysis
R491 increases the fraction and number of small focal adhesions. (A) Representative confocal <t>microscopy</t> images of BJ-Ras cells treated with 5 μM control or R491, showing vimentin, phospho-tyrosine, F-actin, as indicated, and merged images with vimentin (red), phospho-tyrosine (yellow), actin (green) and nuclei (blue). Inset images: magnified views of boxed areas in the larger images. Scale bars: 10 μm. The graphs show (B) the average size of cell-matrix adhesions/per cell, with n = 516 and 478 focal adhesions for control- and R491-treated cells, respectively, and (C) the frequency distribution of the binned sizes of focal adhesions of control- (black) or R491- (grey) treated cells. ** p ≤ 0.01. The difference in the frequency distribution was significant with p ≤ 0.0001.
Traction Force Microscopy Data Analysis, supplied by GraphPad Software Inc, 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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3d raman microscopy data  (HORIBA Ltd)
90
HORIBA Ltd 3d raman microscopy data
R491 increases the fraction and number of small focal adhesions. (A) Representative confocal <t>microscopy</t> images of BJ-Ras cells treated with 5 μM control or R491, showing vimentin, phospho-tyrosine, F-actin, as indicated, and merged images with vimentin (red), phospho-tyrosine (yellow), actin (green) and nuclei (blue). Inset images: magnified views of boxed areas in the larger images. Scale bars: 10 μm. The graphs show (B) the average size of cell-matrix adhesions/per cell, with n = 516 and 478 focal adhesions for control- and R491-treated cells, respectively, and (C) the frequency distribution of the binned sizes of focal adhesions of control- (black) or R491- (grey) treated cells. ** p ≤ 0.01. The difference in the frequency distribution was significant with p ≤ 0.0001.
3d Raman Microscopy Data, supplied by HORIBA Ltd, 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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hildebrand dgc 2017 multi-resolution serial-section electron microscopy data set  (Neurodata GmbH)
90
Neurodata GmbH hildebrand dgc 2017 multi-resolution serial-section electron microscopy data set
R491 increases the fraction and number of small focal adhesions. (A) Representative confocal <t>microscopy</t> images of BJ-Ras cells treated with 5 μM control or R491, showing vimentin, phospho-tyrosine, F-actin, as indicated, and merged images with vimentin (red), phospho-tyrosine (yellow), actin (green) and nuclei (blue). Inset images: magnified views of boxed areas in the larger images. Scale bars: 10 μm. The graphs show (B) the average size of cell-matrix adhesions/per cell, with n = 516 and 478 focal adhesions for control- and R491-treated cells, respectively, and (C) the frequency distribution of the binned sizes of focal adhesions of control- (black) or R491- (grey) treated cells. ** p ≤ 0.01. The difference in the frequency distribution was significant with p ≤ 0.0001.
Hildebrand Dgc 2017 Multi Resolution Serial Section Electron Microscopy Data Set, supplied by Neurodata GmbH, 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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microscopy data  (Viollier AG)
90
Viollier AG microscopy data
R491 increases the fraction and number of small focal adhesions. (A) Representative confocal <t>microscopy</t> images of BJ-Ras cells treated with 5 μM control or R491, showing vimentin, phospho-tyrosine, F-actin, as indicated, and merged images with vimentin (red), phospho-tyrosine (yellow), actin (green) and nuclei (blue). Inset images: magnified views of boxed areas in the larger images. Scale bars: 10 μm. The graphs show (B) the average size of cell-matrix adhesions/per cell, with n = 516 and 478 focal adhesions for control- and R491-treated cells, respectively, and (C) the frequency distribution of the binned sizes of focal adhesions of control- (black) or R491- (grey) treated cells. ** p ≤ 0.01. The difference in the frequency distribution was significant with p ≤ 0.0001.
Microscopy Data, supplied by Viollier AG, 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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scanning probe microscopy data analysis software nova  (NT MDT America Inc)
90
NT MDT America Inc scanning probe microscopy data analysis software nova
R491 increases the fraction and number of small focal adhesions. (A) Representative confocal <t>microscopy</t> images of BJ-Ras cells treated with 5 μM control or R491, showing vimentin, phospho-tyrosine, F-actin, as indicated, and merged images with vimentin (red), phospho-tyrosine (yellow), actin (green) and nuclei (blue). Inset images: magnified views of boxed areas in the larger images. Scale bars: 10 μm. The graphs show (B) the average size of cell-matrix adhesions/per cell, with n = 516 and 478 focal adhesions for control- and R491-treated cells, respectively, and (C) the frequency distribution of the binned sizes of focal adhesions of control- (black) or R491- (grey) treated cells. ** p ≤ 0.01. The difference in the frequency distribution was significant with p ≤ 0.0001.
Scanning Probe Microscopy Data Analysis Software Nova, supplied by NT MDT America Inc, 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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light microscopy data set  (Bachofen AG)
90
Bachofen AG light microscopy data set
R491 increases the fraction and number of small focal adhesions. (A) Representative confocal <t>microscopy</t> images of BJ-Ras cells treated with 5 μM control or R491, showing vimentin, phospho-tyrosine, F-actin, as indicated, and merged images with vimentin (red), phospho-tyrosine (yellow), actin (green) and nuclei (blue). Inset images: magnified views of boxed areas in the larger images. Scale bars: 10 μm. The graphs show (B) the average size of cell-matrix adhesions/per cell, with n = 516 and 478 focal adhesions for control- and R491-treated cells, respectively, and (C) the frequency distribution of the binned sizes of focal adhesions of control- (black) or R491- (grey) treated cells. ** p ≤ 0.01. The difference in the frequency distribution was significant with p ≤ 0.0001.
Light Microscopy Data Set, supplied by Bachofen AG, 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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fluorescence microscopy data analysis  (GraphPad Software Inc)
90
GraphPad Software Inc fluorescence microscopy data analysis
R491 increases the fraction and number of small focal adhesions. (A) Representative confocal <t>microscopy</t> images of BJ-Ras cells treated with 5 μM control or R491, showing vimentin, phospho-tyrosine, F-actin, as indicated, and merged images with vimentin (red), phospho-tyrosine (yellow), actin (green) and nuclei (blue). Inset images: magnified views of boxed areas in the larger images. Scale bars: 10 μm. The graphs show (B) the average size of cell-matrix adhesions/per cell, with n = 516 and 478 focal adhesions for control- and R491-treated cells, respectively, and (C) the frequency distribution of the binned sizes of focal adhesions of control- (black) or R491- (grey) treated cells. ** p ≤ 0.01. The difference in the frequency distribution was significant with p ≤ 0.0001.
Fluorescence Microscopy Data Analysis, supplied by GraphPad Software Inc, 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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Image Search Results


R491 increases the fraction and number of small focal adhesions. (A) Representative confocal microscopy images of BJ-Ras cells treated with 5 μM control or R491, showing vimentin, phospho-tyrosine, F-actin, as indicated, and merged images with vimentin (red), phospho-tyrosine (yellow), actin (green) and nuclei (blue). Inset images: magnified views of boxed areas in the larger images. Scale bars: 10 μm. The graphs show (B) the average size of cell-matrix adhesions/per cell, with n = 516 and 478 focal adhesions for control- and R491-treated cells, respectively, and (C) the frequency distribution of the binned sizes of focal adhesions of control- (black) or R491- (grey) treated cells. ** p ≤ 0.01. The difference in the frequency distribution was significant with p ≤ 0.0001.

Journal: Frontiers in Cell and Developmental Biology

Article Title: ALD-R491 regulates vimentin filament stability and solubility, cell contractile force, cell migration speed and directionality

doi: 10.3389/fcell.2022.926283

Figure Lengend Snippet: R491 increases the fraction and number of small focal adhesions. (A) Representative confocal microscopy images of BJ-Ras cells treated with 5 μM control or R491, showing vimentin, phospho-tyrosine, F-actin, as indicated, and merged images with vimentin (red), phospho-tyrosine (yellow), actin (green) and nuclei (blue). Inset images: magnified views of boxed areas in the larger images. Scale bars: 10 μm. The graphs show (B) the average size of cell-matrix adhesions/per cell, with n = 516 and 478 focal adhesions for control- and R491-treated cells, respectively, and (C) the frequency distribution of the binned sizes of focal adhesions of control- (black) or R491- (grey) treated cells. ** p ≤ 0.01. The difference in the frequency distribution was significant with p ≤ 0.0001.

Article Snippet: The mean values of the aspect ratio, cell migration speed and persistence, cells from which debris is detached and left behind during migration, filament distribution, as well as Traction force microscopy data were analyzed using GraphPad Prism (v.9.3.1).

Techniques: Confocal Microscopy, Control