wet western blot apparatus (miniprotean iv) Search Results


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Figure 5. Western blotting analysis of IEC6 cells infected by the different S. Typhimurium strains. Alteration of Extracellular Matrix Proteins (ECM) after bacterial invasion is illustrated by western blotting analysis of laminin and fibronectin. Bacteria were deposited on IEC-6 with a multiplicity of infection of 10, for 1.5 h, followed by gentamicin (100µg/ml) for 1.5 h. Cells were then resuspended in Laemmli buffer and denaturated 10 min at 100°C. Samples from Non-infected cells (NI) and cells infected by STM-ZT, STM-Z, STM-T or STM-3d strains were loaded in a 4-15% <t>Miniprotean</t> <t>TGX</t> Precast Protein gels and then transferred to a nitrocellulose membrane followed by detection of laminin (A) and fibronectin (B). Protein concentrations were normalized to the tubulin-blotting reference and the ratios were expressed relative to non-infected cells. The Regions of interest (ROI) taking into account for this normalization are represented by the rectangles.
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Figure 5. Western blotting analysis of IEC6 cells infected by the different S. Typhimurium strains. Alteration of Extracellular Matrix Proteins (ECM) after bacterial invasion is illustrated by western blotting analysis of laminin and fibronectin. Bacteria were deposited on IEC-6 with a multiplicity of infection of 10, for 1.5 h, followed by gentamicin (100µg/ml) for 1.5 h. Cells were then resuspended in Laemmli buffer and denaturated 10 min at 100°C. Samples from Non-infected cells (NI) and cells infected by STM-ZT, STM-Z, STM-T or STM-3d strains were loaded in a 4-15% <t>Miniprotean</t> <t>TGX</t> Precast Protein gels and then transferred to a nitrocellulose membrane followed by detection of laminin (A) and fibronectin (B). Protein concentrations were normalized to the tubulin-blotting reference and the ratios were expressed relative to non-infected cells. The Regions of interest (ROI) taking into account for this normalization are represented by the rectangles.
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Figure 5. Western blotting analysis of IEC6 cells infected by the different S. Typhimurium strains. Alteration of Extracellular Matrix Proteins (ECM) after bacterial invasion is illustrated by western blotting analysis of laminin and fibronectin. Bacteria were deposited on IEC-6 with a multiplicity of infection of 10, for 1.5 h, followed by gentamicin (100µg/ml) for 1.5 h. Cells were then resuspended in Laemmli buffer and denaturated 10 min at 100°C. Samples from Non-infected cells (NI) and cells infected by STM-ZT, STM-Z, STM-T or STM-3d strains were loaded in a 4-15% <t>Miniprotean</t> <t>TGX</t> Precast Protein gels and then transferred to a nitrocellulose membrane followed by detection of laminin (A) and fibronectin (B). Protein concentrations were normalized to the tubulin-blotting reference and the ratios were expressed relative to non-infected cells. The Regions of interest (ROI) taking into account for this normalization are represented by the rectangles.
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miniprotean system  (Bio-Rad)
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Figure 5. Western blotting analysis of IEC6 cells infected by the different S. Typhimurium strains. Alteration of Extracellular Matrix Proteins (ECM) after bacterial invasion is illustrated by western blotting analysis of laminin and fibronectin. Bacteria were deposited on IEC-6 with a multiplicity of infection of 10, for 1.5 h, followed by gentamicin (100µg/ml) for 1.5 h. Cells were then resuspended in Laemmli buffer and denaturated 10 min at 100°C. Samples from Non-infected cells (NI) and cells infected by STM-ZT, STM-Z, STM-T or STM-3d strains were loaded in a 4-15% <t>Miniprotean</t> <t>TGX</t> Precast Protein gels and then transferred to a nitrocellulose membrane followed by detection of laminin (A) and fibronectin (B). Protein concentrations were normalized to the tubulin-blotting reference and the ratios were expressed relative to non-infected cells. The Regions of interest (ROI) taking into account for this normalization are represented by the rectangles.
Miniprotean System, supplied by Bio-Rad, 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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Figure 5. Western blotting analysis of IEC6 cells infected by the different S. Typhimurium strains. Alteration of Extracellular Matrix Proteins (ECM) after bacterial invasion is illustrated by western blotting analysis of laminin and fibronectin. Bacteria were deposited on IEC-6 with a multiplicity of infection of 10, for 1.5 h, followed by gentamicin (100µg/ml) for 1.5 h. Cells were then resuspended in Laemmli buffer and denaturated 10 min at 100°C. Samples from Non-infected cells (NI) and cells infected by STM-ZT, STM-Z, STM-T or STM-3d strains were loaded in a 4-15% <t>Miniprotean</t> <t>TGX</t> Precast Protein gels and then transferred to a nitrocellulose membrane followed by detection of laminin (A) and fibronectin (B). Protein concentrations were normalized to the tubulin-blotting reference and the ratios were expressed relative to non-infected cells. The Regions of interest (ROI) taking into account for this normalization are represented by the rectangles.
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miniprotean tgx  (Bio-Rad)
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Figure 5. Western blotting analysis of IEC6 cells infected by the different S. Typhimurium strains. Alteration of Extracellular Matrix Proteins (ECM) after bacterial invasion is illustrated by western blotting analysis of laminin and fibronectin. Bacteria were deposited on IEC-6 with a multiplicity of infection of 10, for 1.5 h, followed by gentamicin (100µg/ml) for 1.5 h. Cells were then resuspended in Laemmli buffer and denaturated 10 min at 100°C. Samples from Non-infected cells (NI) and cells infected by STM-ZT, STM-Z, STM-T or STM-3d strains were loaded in a 4-15% <t>Miniprotean</t> <t>TGX</t> Precast Protein gels and then transferred to a nitrocellulose membrane followed by detection of laminin (A) and fibronectin (B). Protein concentrations were normalized to the tubulin-blotting reference and the ratios were expressed relative to non-infected cells. The Regions of interest (ROI) taking into account for this normalization are represented by the rectangles.
Miniprotean Tgx, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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95
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Figure 5. Western blotting analysis of IEC6 cells infected by the different S. Typhimurium strains. Alteration of Extracellular Matrix Proteins (ECM) after bacterial invasion is illustrated by western blotting analysis of laminin and fibronectin. Bacteria were deposited on IEC-6 with a multiplicity of infection of 10, for 1.5 h, followed by gentamicin (100µg/ml) for 1.5 h. Cells were then resuspended in Laemmli buffer and denaturated 10 min at 100°C. Samples from Non-infected cells (NI) and cells infected by STM-ZT, STM-Z, STM-T or STM-3d strains were loaded in a 4-15% <t>Miniprotean</t> <t>TGX</t> Precast Protein gels and then transferred to a nitrocellulose membrane followed by detection of laminin (A) and fibronectin (B). Protein concentrations were normalized to the tubulin-blotting reference and the ratios were expressed relative to non-infected cells. The Regions of interest (ROI) taking into account for this normalization are represented by the rectangles.
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miniprotean western blotting wet transfer module  (Bio-Rad)
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Figure 5. Western blotting analysis of IEC6 cells infected by the different S. Typhimurium strains. Alteration of Extracellular Matrix Proteins (ECM) after bacterial invasion is illustrated by western blotting analysis of laminin and fibronectin. Bacteria were deposited on IEC-6 with a multiplicity of infection of 10, for 1.5 h, followed by gentamicin (100µg/ml) for 1.5 h. Cells were then resuspended in Laemmli buffer and denaturated 10 min at 100°C. Samples from Non-infected cells (NI) and cells infected by STM-ZT, STM-Z, STM-T or STM-3d strains were loaded in a 4-15% <t>Miniprotean</t> <t>TGX</t> Precast Protein gels and then transferred to a nitrocellulose membrane followed by detection of laminin (A) and fibronectin (B). Protein concentrations were normalized to the tubulin-blotting reference and the ratios were expressed relative to non-infected cells. The Regions of interest (ROI) taking into account for this normalization are represented by the rectangles.
Miniprotean Western Blotting Wet Transfer Module, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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western blot miniprotean system  (Bio-Rad)
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Bio-Rad western blot miniprotean system
Figure 5. Western blotting analysis of IEC6 cells infected by the different S. Typhimurium strains. Alteration of Extracellular Matrix Proteins (ECM) after bacterial invasion is illustrated by western blotting analysis of laminin and fibronectin. Bacteria were deposited on IEC-6 with a multiplicity of infection of 10, for 1.5 h, followed by gentamicin (100µg/ml) for 1.5 h. Cells were then resuspended in Laemmli buffer and denaturated 10 min at 100°C. Samples from Non-infected cells (NI) and cells infected by STM-ZT, STM-Z, STM-T or STM-3d strains were loaded in a 4-15% <t>Miniprotean</t> <t>TGX</t> Precast Protein gels and then transferred to a nitrocellulose membrane followed by detection of laminin (A) and fibronectin (B). Protein concentrations were normalized to the tubulin-blotting reference and the ratios were expressed relative to non-infected cells. The Regions of interest (ROI) taking into account for this normalization are represented by the rectangles.
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miniprotean gels  (Bio-Rad)
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Figure 5. Western blotting analysis of IEC6 cells infected by the different S. Typhimurium strains. Alteration of Extracellular Matrix Proteins (ECM) after bacterial invasion is illustrated by western blotting analysis of laminin and fibronectin. Bacteria were deposited on IEC-6 with a multiplicity of infection of 10, for 1.5 h, followed by gentamicin (100µg/ml) for 1.5 h. Cells were then resuspended in Laemmli buffer and denaturated 10 min at 100°C. Samples from Non-infected cells (NI) and cells infected by STM-ZT, STM-Z, STM-T or STM-3d strains were loaded in a 4-15% <t>Miniprotean</t> <t>TGX</t> Precast Protein gels and then transferred to a nitrocellulose membrane followed by detection of laminin (A) and fibronectin (B). Protein concentrations were normalized to the tubulin-blotting reference and the ratios were expressed relative to non-infected cells. The Regions of interest (ROI) taking into account for this normalization are represented by the rectangles.
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miniprotean precast gel  (Bio-Rad)
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Figure 5. Western blotting analysis of IEC6 cells infected by the different S. Typhimurium strains. Alteration of Extracellular Matrix Proteins (ECM) after bacterial invasion is illustrated by western blotting analysis of laminin and fibronectin. Bacteria were deposited on IEC-6 with a multiplicity of infection of 10, for 1.5 h, followed by gentamicin (100µg/ml) for 1.5 h. Cells were then resuspended in Laemmli buffer and denaturated 10 min at 100°C. Samples from Non-infected cells (NI) and cells infected by STM-ZT, STM-Z, STM-T or STM-3d strains were loaded in a 4-15% <t>Miniprotean</t> <t>TGX</t> Precast Protein gels and then transferred to a nitrocellulose membrane followed by detection of laminin (A) and fibronectin (B). Protein concentrations were normalized to the tubulin-blotting reference and the ratios were expressed relative to non-infected cells. The Regions of interest (ROI) taking into account for this normalization are represented by the rectangles.
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Figure 5. Western blotting analysis of IEC6 cells infected by the different S. Typhimurium strains. Alteration of Extracellular Matrix Proteins (ECM) after bacterial invasion is illustrated by western blotting analysis of laminin and fibronectin. Bacteria were deposited on IEC-6 with a multiplicity of infection of 10, for 1.5 h, followed by gentamicin (100µg/ml) for 1.5 h. Cells were then resuspended in Laemmli buffer and denaturated 10 min at 100°C. Samples from Non-infected cells (NI) and cells infected by STM-ZT, STM-Z, STM-T or STM-3d strains were loaded in a 4-15% Miniprotean TGX Precast Protein gels and then transferred to a nitrocellulose membrane followed by detection of laminin (A) and fibronectin (B). Protein concentrations were normalized to the tubulin-blotting reference and the ratios were expressed relative to non-infected cells. The Regions of interest (ROI) taking into account for this normalization are represented by the rectangles.

Journal: Virulence

Article Title: Epithelial cell invasion by salmonella typhimurium induces modulation of genes controlled by aryl hydrocarbon receptor signaling and involved in extracellular matrix biogenesis.

doi: 10.1080/21505594.2022.2158663

Figure Lengend Snippet: Figure 5. Western blotting analysis of IEC6 cells infected by the different S. Typhimurium strains. Alteration of Extracellular Matrix Proteins (ECM) after bacterial invasion is illustrated by western blotting analysis of laminin and fibronectin. Bacteria were deposited on IEC-6 with a multiplicity of infection of 10, for 1.5 h, followed by gentamicin (100µg/ml) for 1.5 h. Cells were then resuspended in Laemmli buffer and denaturated 10 min at 100°C. Samples from Non-infected cells (NI) and cells infected by STM-ZT, STM-Z, STM-T or STM-3d strains were loaded in a 4-15% Miniprotean TGX Precast Protein gels and then transferred to a nitrocellulose membrane followed by detection of laminin (A) and fibronectin (B). Protein concentrations were normalized to the tubulin-blotting reference and the ratios were expressed relative to non-infected cells. The Regions of interest (ROI) taking into account for this normalization are represented by the rectangles.

Article Snippet: Whole-cell protein samples 25 μL were run on SDS- PAGE (100 V) in a 4–15% Miniprotean TGX Precast Protein gels (Bio-Rad) in a Tris-glycine running buffer (25 mM Tris base, 192 mM glycine, 0.1% [wt/ vol] SDS [pH 8.31]) and transferred onto a nitrocellulose membrane with Trans-blot Turbo transfer System (Bio-Rad) in Tris-glycine buffer system 15 min at 25 V and 2.5 mA.

Techniques: Western Blot, Infection, Bacteria, Membrane