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Image Search Results
Journal: BMC Microbiology
Article Title: Nontypeable Haemophilus influenzae exploits the interaction between protein-E and vitronectin for the adherence and invasion to bronchial epithelial cells
doi: 10.1186/s12866-015-0600-8
Figure Lengend Snippet: NTHi binding of immobilized vitronectin in the absence or presence of heparin. Human plasma vitronectin was bound to glass-bottomed dishes. NTHi was incubated on the plate-bound vitronectin for 30 minutes, and then the dishes were washed three times. In some experiments, plate-bound vitronectin was pretreated with heparin before incubation with NTHi. NTHi was stained with LIVE/DEAD®. Live NTHi is stained green. BSA was used as a negative control. Representative fluorescent micrographs show that both NTHi strains (ATCC 19418 ( a ) and HUSM 0481 ( b )) attached to plate-bound vitronectin and that this attachment is blocked by heparin. White bars represent 10 μm. Summaries of the numbers of attached NTHi (per field at 1,000× magnification) are shown in ( c ) for ATCC 19418 and ( d ) for HUSM 0481. Error bars represent SEM in three independent experiments that gave similar results. ** p < 0.01
Article Snippet: After washing with PBS, 5.0 μg/ml of monoclonal antibody to
Techniques: Binding Assay, Incubation, Staining, Negative Control
Journal: BMC Microbiology
Article Title: Nontypeable Haemophilus influenzae exploits the interaction between protein-E and vitronectin for the adherence and invasion to bronchial epithelial cells
doi: 10.1186/s12866-015-0600-8
Figure Lengend Snippet: Binding of NTHi to immobilized vitronectin in the presence of protein-E peptide. Human plasma vitronectin was bound to glass-bottomed dishes. NTHi (HUSM 0481) was incubated on the plate-bound vitronectin for 30 minutes, and then the dishes were washed three times. In some experiments, plate-bound vitronectin was pretreated with protein-E peptide (PE 84–108 ) before incubation with NTHi. BSA was used as a negative control. NTHi was stained with LIVE/DEAD®, and viable NTHi is stained green. a Representative fluorescent micrographs of NTHi incubated on plate-bound vitronectin that was untreated or pretreated with PE 84–108 . White bars represent 10 μm. b The number of attached NTHi per field at 1,000 × magnification that was pretreated with increasing concentrations of PE 84–108 . Error bars represent SEM in three independent experiments that gave similar results. ** p < 0.01
Article Snippet: After washing with PBS, 5.0 μg/ml of monoclonal antibody to
Techniques: Binding Assay, Incubation, Negative Control, Staining
Journal: BMC Microbiology
Article Title: Nontypeable Haemophilus influenzae exploits the interaction between protein-E and vitronectin for the adherence and invasion to bronchial epithelial cells
doi: 10.1186/s12866-015-0600-8
Figure Lengend Snippet: A schema of the proposed mechanism by which NTHi penetrates into bronchial epithelial cell via protein-E and vitronectin. Vitronectin has three heparin-binding domains (HBDs), which interact with NTHi. Of those HBDs, the C-terminal HBD-3 corresponds to a protein-E binding region and interacts with PE 84–108 . This interaction is blocked by heparin or PE 84–108 peptide. Vitronectin also possesses a cell receptor binding site characterized by an Arg-Gly-Asp (RGD) sequence, which interacts with integrins on the bronchial epithelial cell surface. This protein-E-vitronectin axis seems to play a role in the adherence and penetration of NTHi into bronchial epithelial cells
Article Snippet: After washing with PBS, 5.0 μg/ml of monoclonal antibody to
Techniques: Binding Assay, Sequencing
Journal: Veterinary Research
Article Title: Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) moonlights as an adhesin in Mycoplasma hyorhinis adhesion to epithelial cells as well as a plasminogen receptor mediating extracellular matrix degradation
doi: 10.1186/s13567-021-00952-8
Figure Lengend Snippet: Binding of the rGAPDH protein to different ECM components in ELISA experiment . Microtiters plate was coated with Matrigel, fibronectin, collagen or laminin solution. Various concentrations of rGAPDH or BSA were added and detected by anti-His-tag monoclonal antibody. For detecting the binding to vitronectin, microtiters plate was coated with rGAPDH or BSA. Various concentrations of vitronectin were added and detected by anti-vitronectin monoclonal antibody. * P < 0.05, ** P < 0.01, compared with the negative control (BSA).
Article Snippet: The bound vitronectin was detected by
Techniques: Binding Assay, Enzyme-linked Immunosorbent Assay, Negative Control
Journal: Journal of Biological Chemistry
Article Title: Plasminogen Activator Inhibitor-1 Regulates Tumor Growth and Angiogenesis
doi: 10.1074/jbc.m105980200
Figure Lengend Snippet: FIG. 3. Immuno-analysis of vessel architecture in M21 tumors. Tumor sections treated with PBS (A, D, G), partially inactivated PAI-1 (B, E, H), or fully active PAI-1 (C, F, I) were stained for the following: immunohistochemical staining for collagen IV (A–C), immunohisto- chemical staining for smooth muscle cell actin (D–F), immunofluores- cence analysis of vitronectin (green) (G–I), endothelial cells (red), and tumor cells (blue). The original magnification for all panels is 400.
Article Snippet: For immunofluorescence staining of tumor sections, slides were treated as above and then double stained with
Techniques: Staining, Immunohistochemical staining
Journal: International Journal of Molecular Sciences
Article Title: Study on the Expression and Clinical Significances of Lewis y Antigen and Integrin αv, β3 in Epithelial Ovarian Tumors
doi: 10.3390/ijms12063409
Figure Lengend Snippet: Expression of integrin αv, β3 in different ovarian tissues.
Article Snippet:
Techniques: Expressing
Journal: International Journal of Molecular Sciences
Article Title: Study on the Expression and Clinical Significances of Lewis y Antigen and Integrin αv, β3 in Epithelial Ovarian Tumors
doi: 10.3390/ijms12063409
Figure Lengend Snippet: Immunohistochemical staining in ovarian malignant tumor ( A1 – A3 ), borderline tumor ( B1 – B3 ), benign tumor ( C1 – C3 ) and normal ovarian tissue ( D1 – D3 ). Integrin αv ( A1 , B1 , C1 , D1 ); β3 ( A2 , B2 , C2 , D2 ) and Lewis y ( A3 , B3 , C3 , D3 ). (Original magnification ×200).
Article Snippet:
Techniques: Immunohistochemical staining, Staining
Journal: International Journal of Molecular Sciences
Article Title: Study on the Expression and Clinical Significances of Lewis y Antigen and Integrin αv, β3 in Epithelial Ovarian Tumors
doi: 10.3390/ijms12063409
Figure Lengend Snippet: Relationship between integrin αv with the clinical and pathological parameters of malignant ovarian cancer.
Article Snippet:
Techniques: Diffusion-based Assay
Journal: International Journal of Molecular Sciences
Article Title: Study on the Expression and Clinical Significances of Lewis y Antigen and Integrin αv, β3 in Epithelial Ovarian Tumors
doi: 10.3390/ijms12063409
Figure Lengend Snippet: Relationship between integrin β3 with the clinical and pathological parameters of malignant ovarian cancer.
Article Snippet:
Techniques: Diffusion-based Assay
Journal: International Journal of Molecular Sciences
Article Title: Study on the Expression and Clinical Significances of Lewis y Antigen and Integrin αv, β3 in Epithelial Ovarian Tumors
doi: 10.3390/ijms12063409
Figure Lengend Snippet: Correlation between expression of Lewis y antigen and integrin αv in ovarian cancer.
Article Snippet:
Techniques: Expressing
Journal: International Journal of Molecular Sciences
Article Title: Study on the Expression and Clinical Significances of Lewis y Antigen and Integrin αv, β3 in Epithelial Ovarian Tumors
doi: 10.3390/ijms12063409
Figure Lengend Snippet: Correlation between expression of Lewis y antigen and integrin β3 in ovarian cancer.
Article Snippet:
Techniques: Expressing
Journal: International Journal of Molecular Sciences
Article Title: Study on the Expression and Clinical Significances of Lewis y Antigen and Integrin αv, β3 in Epithelial Ovarian Tumors
doi: 10.3390/ijms12063409
Figure Lengend Snippet: Integrin αv, β3 and Lewis y colocalize in ovarian malignant tumor. Using an immunofluorescent double-labeling method. Integrin αv and β3 ( A1 and B1 ); Lewis y ( A2 and B2 ); nucleus ( A3 and B3 ); Merged image ( A4 and B4 ). (Original magnification ×400).
Article Snippet:
Techniques: Labeling