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An ELISA kit for the detection of VEGF C Human This uses Sandwich ELISA Double Antibody and has a sensitivity of 65 625pg ml
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Image Search Results
Journal: Chinese Journal of Cancer Research
Article Title: Tim-3 promotes cell aggressiveness and paclitaxel resistance through NF-κB/STAT3 signalling pathway in breast cancer cells
doi: 10.21147/j.issn.1000-9604.2020.05.02
Figure Lengend Snippet: VEGFC and VEGFR2 protein levels in conditioned media of stable cell lines indicated by ELISA. (A) VEGFC; (B) VEGFR2. VEGF, vascular endothelial growth factor; ELISA, enzyme-linked immunosorbent assay.
Article Snippet: ELISA was performed using the
Techniques: Stable Transfection, Enzyme-linked Immunosorbent Assay
Journal: Frontiers in immunology
Article Title: Promotion of BST2 expression by the transcription factor IRF6 affects the progression of endometriosis.
doi: 10.3389/fimmu.2023.1115504
Figure Lengend Snippet: FIGURE 1 BST2 levels were overexpressed and positively correlated with the lymphangiogenesis in the endometriosis. (A), BST2 expression levels in the GSE7305 and GSE7307 datasets. (B–D), BST2 mRNA (B) and protein (C, D) expression in endometriosis samples. (E), LYVE1 expression levels in the GSE7305 and GSE7307 datasets. (F), The correlation of BST2 expression and VEGFC expression in the GSE7305 and GSE7307 datasets. (G), The correlation of VEGFC expression and LYVE1 expression in the GSE7305 and GSE7307 datasets. (H), (H, E) staining and Immunohistochemistry (IHC) of BST2, VEGFC and LYVE1 in endometriosis and control group. *p < 0.05; **p < 0.01; ***p < 0.001; ****p < 0.0001.
Article Snippet: The concentrations of human VEGFC in the cell culture supernatants were measured with a
Techniques: Expressing, Staining, Immunohistochemistry, Control
Journal: Frontiers in immunology
Article Title: Promotion of BST2 expression by the transcription factor IRF6 affects the progression of endometriosis.
doi: 10.3389/fimmu.2023.1115504
Figure Lengend Snippet: FIGURE 5 Effect of the conditioned medium (CM) of EESCs with BST2 knockdown on HLECs. (A), The Tube formation assay was conducted to check the tube formation ability with the CM of EESCs with BST2 knockdown on HLECs. (B), CCK-8 assay showing the proliferation of HLECs treated with CM from Si-BST2 or Si-NC EESCs for 24h. (C, D), Scratch assay (C) and transwell assay (D) were conducted to assess migration ability of HLECs treated with CM from Si-BST2 or Si-NC EESCs for 24h. (E), The VEGFC protein expression was measured by western blot analysis after transfection with Si-BST2 or Si-NC for 48h. (F), The VEGFC expression from the conditioned medium (CM) of EESCs with BST2 knockdown was detected by ELISA assay. *p < 0.05; **p < 0.01; ****p < 0.0001.
Article Snippet: The concentrations of human VEGFC in the cell culture supernatants were measured with a
Techniques: Knockdown, Tube Formation Assay, CCK-8 Assay, Wound Healing Assay, Transwell Assay, Migration, Expressing, Western Blot, Transfection, Enzyme-linked Immunosorbent Assay
Journal: Frontiers in immunology
Article Title: Promotion of BST2 expression by the transcription factor IRF6 affects the progression of endometriosis.
doi: 10.3389/fimmu.2023.1115504
Figure Lengend Snippet: FIGURE 8 BST2 promoted migration and lymphangiogenesis of EESCs via the NF-kB signaling pathway. (A, B), The wound healing assays (A) and the transwell assay (B) were performed to measure the cell migration ability of EESCs after transfection with Si-BST2 and/or IL-1b. (C), The western blot analysis was used to examine the migration-related protein after transfection with Si-BST2 and/or IL-1b. (D, E), The tube formation assay was conducted to check the tube formation ability with the CM of EESCs with Si-BST2 and/or IL-1b on HLECs. (F), The western blot analysis was used to measure the VEGFC after transfection with Si-BST2 and/or IL-1b. *p < 0.05; **p < 0.01; ***p < 0.001.
Article Snippet: The concentrations of human VEGFC in the cell culture supernatants were measured with a
Techniques: Migration, Transwell Assay, Transfection, Western Blot, Tube Formation Assay
Journal: Frontiers in immunology
Article Title: Promotion of BST2 expression by the transcription factor IRF6 affects the progression of endometriosis.
doi: 10.3389/fimmu.2023.1115504
Figure Lengend Snippet: FIGURE 11 BST2 partially rescued the effects of IRF6 on the migration and lymphangiogenesis in EESCs. (A, B), Wound healing assay (A) and Transwell assay (B) detected the cell migration ability after transfection with Oe-IRF6 and/or Si-BST2 for 48h. (C), The western blot analysis examined the migration- related proteins after transfection with Oe-IRF6 and/or Si-BST2 for 48h. (D), The tube formation assay checked the tube formation ability with the CM of EESCs transfected with Oe-IRF6 and/or Si-BST2 on HLECs. (E), The western blot analysis measured the VEGFC after transfection with Oe-IRF6 and/or Si-BST2. *p < 0.05; **p < 0.01; ***p < 0.001.
Article Snippet: The concentrations of human VEGFC in the cell culture supernatants were measured with a
Techniques: Migration, Wound Healing Assay, Transwell Assay, Transfection, Western Blot, Tube Formation Assay
Journal: Oncology Research
Article Title: Exosomal miR-224-3p promotes lymphangiogenesis and lymph node metastasis by targeting GSK3B in gastric cancer
doi: 10.32604/or.2024.050431
Figure Lengend Snippet: Exosomal miR-224 was screened to be associated with LNM of GC (A) Volcano plot analysis of serum sequencing differential miRNAs (LNM vs . nonLNM). (B) Venn diagram of the serum sequencing differential dataset vs . the GEO dataset. (C) Relative expression of serum miR-224-3p in HC and GC in GSE112264 datasets. (D) Relative expression of serum miR-224-3p in nonLNM and LNM. (E) Correlation analysis between the relative expression of serum miR-224-3p and serum VEGFC. (F) Relative expression of miR-224-3p in serum EVs and exo-free serum. (G) Schematic diagram of LVD in tumor tissues. (H) Correlation analysis between the relative expression of serum miR-224-3p and LVD in tumor tissues. * p -value < 0.05, ** p -value < 0.01, *** p -value < 0.001.
Article Snippet: The remaining steps of
Techniques: Sequencing, Expressing