anti fak antibody (Cell Signaling Technology Inc)
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Anti Fak Antibody, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 2777 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fak/FAK+Antibody/pm42894734-147-35-38
Average 96 stars, based on 2777 article reviews
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Blocking Assay:Article Title: Spatially defined bioprinting of detrusor and sphincter mimetics uncovers paracrine-mediated contraction dyssynergia Article Snippet: .. After blocking with non-fat milk, the membranes were incubated with primary antibodies against integrin αvβ3 (Abcam, ab78269), LRP1 (Abcam, ab92544), Incubation:Article Title: Spatially defined bioprinting of detrusor and sphincter mimetics uncovers paracrine-mediated contraction dyssynergia Article Snippet: .. After blocking with non-fat milk, the membranes were incubated with primary antibodies against integrin αvβ3 (Abcam, ab78269), LRP1 (Abcam, ab92544), Article Title: Endothelial SMAD1-MCAM axis facilitates sunitinib resistance and progression of clear cell renal cell carcinoma via LAMB1-ITGB1 signaling. Article Snippet: Clear cell renal cell carcinoma (ccRCC) is characterized by high metastatic potential and frequent resistance to conventional therapies, highlighting the need for a deeper understanding of its tumor microenvironment.. Here, we integrated single-cell RNA sequencing and spatial transcriptomics from large ccRCC cohorts to map the cellular landscape of ccRCC.. We identified a distinct stromal cell subpopulation, Melanoma Cell Adhesion Molecule, MCAM endothelial cells (MCAM ECs), which spatially associates with EMT-like tumor cells and promotes disease progression. Electrophoresis:Article Title: Compositions and methods for increasing cancer cell sensitivity to alternating electric fields Article Snippet: Samples were run on SDS-polyacrylamide gel electrophoresis (Bolt 8% Bis-Tris base gel NW00080BOX, Thermo-Fischer). .. After electrophoresis, proteins were transferred to 0.2 μm polyvinylidene difluoride membrane (Immuno-Blot PVDF #162-0177, Bio-Rad) and probed with the appropriate primary antibody: GAPDH (SC-32233, Santa Cruz), Vinculin (ab140007, Abcam), Cyclin D1 (2922, Cell Signaling), Rb (9309, Cell Signaling), pRb S807/811 (8516, Cell Signaling), pAkt 5473, (4051, Cell signaling), Akt (2920, Cell signaling)), Membrane:Article Title: Compositions and methods for increasing cancer cell sensitivity to alternating electric fields Article Snippet: Samples were run on SDS-polyacrylamide gel electrophoresis (Bolt 8% Bis-Tris base gel NW00080BOX, Thermo-Fischer). .. After electrophoresis, proteins were transferred to 0.2 μm polyvinylidene difluoride membrane (Immuno-Blot PVDF #162-0177, Bio-Rad) and probed with the appropriate primary antibody: GAPDH (SC-32233, Santa Cruz), Vinculin (ab140007, Abcam), Cyclin D1 (2922, Cell Signaling), Rb (9309, Cell Signaling), pRb S807/811 (8516, Cell Signaling), pAkt 5473, (4051, Cell signaling), Akt (2920, Cell signaling)), Western Blot:Article Title: VS-4718 enhances apoptosis induced by low-dose carfilzomib and overcomes carfilzomib resistance in PSMB5-mutated proteasome inhibitor resistant multiple myeloma. Article Snippet: .. AR TIC LE IN PR ES S ARTICLE IN PRESS Western blots were accomplished as previously described [19] using antibodies from Cell Signaling Technologies (Danvers, MA, USA) against the following targets: PYK2 ((H364), #3090, 1:1000), pPYK2 ((Y402) #3291, 1:2000), other:Article Title: Aberrant expression of the testis kinase TSSK6activates FAK–STAT3 signaling to promote tumorigenic growth Article Snippet: Antibodies used: TSSK6 (sc-514076, Santa Cruz) (1:500 IB), STAT3 (sc-8019, Santa Cruz (1:1000 IB), |
![Q209R preferentially engages FAK‐YAP signaling. (A) Western blot analysis of GNAQ, BAP1, Melan‐A, p‐ERK1/2 (Thr202/Tyr204), ERK1/2, FRA1, p‐AKT (Ser473), AKT, p‐4EBP1 (Ser65), and 4EBP1 expression in mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . HSP90 was used as an internal loading control. (B) Quantification of the relative ratio between p‐AKT (Ser473) and AKT in Q209R and Q209L UM cell lines from (A). (C) Quantification of the relative ratio between p‐4EBP1 (Ser65) and 4EBP1 in Q209R and Q209L UM cell lines from (A). (D) Western blot analysis of p‐FAK <t>(Tyr397),</t> FAK, p‐YAP (Ser127), and YAP in mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . HSP90 was used as an internal loading control. (E) Quantification of the relative ratio between p‐FAK (Tyr397) and FAK in Q209R and Q209L UM cell lines from (D). (F) Quantification of the relative ratio between p‐YAP (Ser127) and YAP in Q209R and Q209L UM cell lines from (D). Orthotopic tumor‐derived cell lines (QBM12.1 [Q209R], QBM12.3 [Q209R], QBM24 [Q209R], QBM45 [Q209L], QBM47 [Q209L]) and liver metastatic lines (QBM12L [Q209R], QBM12L2 [Q209R], QBM51L [Q209L], QBM53L [Q209L]) were used in A–F. (G) Representative IHC images showing YAP expression in primary tumors from Gnaq CA ; Bap1 CKO ; Myc CKI mice harboring either GNAQ Q209R or GNAQ Q209L . (H) Quantification of the nuclear‐to‐cytoplasmic YAP intensity ratio (H‐score) among primary tumors from Gnaq CA ; Bap1 CKO ; Myc CKI mice harboring either GNAQ Q209R or GNAQ Q209L . (I) Representative IHC images showing YAP expression in liver metastasis derived from intrasplenic transplantation of mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . (J) Quantification of nuclear YAP intensity (H‐score) among liver metastasis derived from intrasplenic transplantation of mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L .](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_5764/pmc13635764/pmc13635764__PCMR-39-0-g001.jpg)