phospho stat2 tyr690 Search Results


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pstat2 cell signaling 907405  (Cell Signaling Technology Inc)
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phospho-stat2 (tyr690  (Beyotime)
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Beyotime phospho-stat2 (tyr690
GBP2 enhances metastasis of ccRCC cells through JAK-STAT signaling. A. Western blotting validation of GBP2 expression in ccRCC cells upon knockdown of GBP2. B. Transwell assays were used to test the migration and invasion abilities upon knockdown of GBP2. * *P < 0.01, * **P < 0.001. Scale bar, 600 µm. C. Western blotting validation of GBP2 expression in ccRCC cells transfected with indicated constructs. D. Transwell assays were used to test the migration and invasion abilities of ACHN and 769-P cells transfected with indicated constructs. * *P < 0.01, * **P < 0.001. Scale bar, 600 µm. E-F. Gene Set Enrichment Analysis revealed that high GBP2 expression was mainly enriched in JAK/STAT signaling based on proteome and transcriptome data from CPTAC (E) and TCGA (F). G. Protein-protein interaction network for GBP2 in ccRCC was constructed using GeneMANIA. Different colors of the network edge indicate the bioinformatics methods applied: physical interaction, predicted, and co-expression. H. The correlation of GBP2 with <t>STAT2/STAT3</t> at both RNA levels (TCGA) and protein levels (CPTAC) in ccRCC was determined. I-J. GBP2 siRNAs (I) or overexpression vectors (J) were transfected into ccRCC cells. The phosphorylation of STAT family proteins was examined by western blotting. K. Transwell assays were used to test the migration abilities of GBP2-expressing ACHN and 769-P cells treated with JAK inhibitor Ruxolitinib. * * P < 0.01, * ** P < 0.001. n.s, no significant. Scale bar, 600 µm.
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Image Search Results


GBP2 enhances metastasis of ccRCC cells through JAK-STAT signaling. A. Western blotting validation of GBP2 expression in ccRCC cells upon knockdown of GBP2. B. Transwell assays were used to test the migration and invasion abilities upon knockdown of GBP2. * *P < 0.01, * **P < 0.001. Scale bar, 600 µm. C. Western blotting validation of GBP2 expression in ccRCC cells transfected with indicated constructs. D. Transwell assays were used to test the migration and invasion abilities of ACHN and 769-P cells transfected with indicated constructs. * *P < 0.01, * **P < 0.001. Scale bar, 600 µm. E-F. Gene Set Enrichment Analysis revealed that high GBP2 expression was mainly enriched in JAK/STAT signaling based on proteome and transcriptome data from CPTAC (E) and TCGA (F). G. Protein-protein interaction network for GBP2 in ccRCC was constructed using GeneMANIA. Different colors of the network edge indicate the bioinformatics methods applied: physical interaction, predicted, and co-expression. H. The correlation of GBP2 with STAT2/STAT3 at both RNA levels (TCGA) and protein levels (CPTAC) in ccRCC was determined. I-J. GBP2 siRNAs (I) or overexpression vectors (J) were transfected into ccRCC cells. The phosphorylation of STAT family proteins was examined by western blotting. K. Transwell assays were used to test the migration abilities of GBP2-expressing ACHN and 769-P cells treated with JAK inhibitor Ruxolitinib. * * P < 0.01, * ** P < 0.001. n.s, no significant. Scale bar, 600 µm.

Journal: Computational and Structural Biotechnology Journal

Article Title: A five-protein prognostic signature with GBP2 functioning in immune cell infiltration of clear cell renal cell carcinoma

doi: 10.1016/j.csbj.2023.04.015

Figure Lengend Snippet: GBP2 enhances metastasis of ccRCC cells through JAK-STAT signaling. A. Western blotting validation of GBP2 expression in ccRCC cells upon knockdown of GBP2. B. Transwell assays were used to test the migration and invasion abilities upon knockdown of GBP2. * *P < 0.01, * **P < 0.001. Scale bar, 600 µm. C. Western blotting validation of GBP2 expression in ccRCC cells transfected with indicated constructs. D. Transwell assays were used to test the migration and invasion abilities of ACHN and 769-P cells transfected with indicated constructs. * *P < 0.01, * **P < 0.001. Scale bar, 600 µm. E-F. Gene Set Enrichment Analysis revealed that high GBP2 expression was mainly enriched in JAK/STAT signaling based on proteome and transcriptome data from CPTAC (E) and TCGA (F). G. Protein-protein interaction network for GBP2 in ccRCC was constructed using GeneMANIA. Different colors of the network edge indicate the bioinformatics methods applied: physical interaction, predicted, and co-expression. H. The correlation of GBP2 with STAT2/STAT3 at both RNA levels (TCGA) and protein levels (CPTAC) in ccRCC was determined. I-J. GBP2 siRNAs (I) or overexpression vectors (J) were transfected into ccRCC cells. The phosphorylation of STAT family proteins was examined by western blotting. K. Transwell assays were used to test the migration abilities of GBP2-expressing ACHN and 769-P cells treated with JAK inhibitor Ruxolitinib. * * P < 0.01, * ** P < 0.001. n.s, no significant. Scale bar, 600 µm.

Article Snippet: STAT1 (Cell Signaling Technology, Boston), STAT2 (Proteintech, Wuhan), STAT3 (Beyotime Biotechnology, Shanghai), Phospho-STAT1 (Tyr701) (Cell Signaling Technology, Boston), Phospho-STAT2 (Tyr690) (Beyotime Biotechnology, Shanghai), Phospho-STAT3 (Tyr705) (Beyotime Biotechnology, Shanghai).

Techniques: Western Blot, Expressing, Migration, Transfection, Construct, Over Expression