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TaKaRa
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BPS Bioscience
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Marlow Industries
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Chassot GmbH
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BioCarta
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Image Search Results
Journal: Heliyon
Article Title: Potential actions of capsaicin for preventing vascular calcification of vascular smooth muscle cells in vitro and in vivo
doi: 10.1016/j.heliyon.2024.e28021
Figure Lengend Snippet: Cap inhibits Pi-induced calcification of VSMCs by inhibiting the Wnt/β-catenin signaling pathway by upregulation of TRPV1 receptor expression. A) RT-qPCR showing the mRNA levels of Wnt3a and β-catenin; B) Western blot illustrating the protein expression levels of Wnt3a and β-catenin; C) Alizarin Red staining assay; D) Calcium content in VSMCs assessed using a calcium colorimetric assay kit. E) RT-qPCR showing the expression of osteogenesis-specific and phenotypic markers in VSMC calcification. F) Western blot depicting the protein expression levels of osteogenesis-specific and phenotypic markers in VSMC calcification; G) Western blot showing the protein expression of β-catenin after treatment with DKK1. VSMCs cultured in the complete and pro-calcifying medium were defined as the control and Pi group, respectively; Pi + Cap: VSMCs cultured in the pro-calcifying medium with 20 μM Cap; Pi + Cap + CPZ: VSMCs cultured in the pro-calcifying medium with 20 μM Cap and 10 μM CPZ; Pi + Cap + DKK1: VSMCs cultured in the pro-calcifying medium with 20 μM Cap and 20 ng/mL DKK1; Data are mean ± SD (n = 3); #: p < 0.05, ##: p < 0.01, ###: p < 0.001 vs Control; *: p < 0.05, **: p < 0.01, ***: p < 0.001 vs Pi; ※: p < 0.05, ※※: p < 0.01, ※※※: p < 0.001 vs Pi + Cap; ns: p > 0.05 vs Control; p > 0.05 vs Pi; p > 0.05 vs Pi + Cap. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Article Snippet: Antibodies against BMP-2 (PRP100126) and Runx2 (ABP53087) were purchased from Abbkine (Wuhan, Hubei, China); SM22α (AF9266) and Wnt3a (DF6113), Affinity Biosciences LTD; β-actin (81115-1-RR), proteintech (Hubei, China); β-catenin (ab32572), Abcom (USA); and
Techniques: Expressing, Quantitative RT-PCR, Western Blot, Staining, Calcium Colorimetric Assay, Cell Culture, Control
Journal: Frontiers in Oncology
Article Title: AXL Overexpression in Tumor-Derived Endothelial Cells Promotes Vessel Metastasis in Patients With Hepatocellular Carcinoma
doi: 10.3389/fonc.2021.650963
Figure Lengend Snippet: AXL/SOX2/DKK-1 axis in HUVECs promotes HCC metastasis. (A) DKK-1 and CCL14 secretion was significantly downregulated in CM from HUVEC-AXL-KD compared with that from HUVEC-AXL-NC, as detected with a human cytokine antibody array. (B) DKK-1 and CCL14 expression was markedly upregulated in the CM of HUVECs overexpressing AXL (CCL14: p < 0.001; DKK-1: p = 0.003) compared with the CM of HUVEC-AXL-NC, as detected by ELISA assay. (C) AXL siRNA downregulated DKK-1 and CCL14 secretion in the CM of HUVEC-AXL-NC and HUVEC-AXL-OE cells (CCL14: p < 0.001 and p < 0.001; DKK-1: p < 0.001 and p < 0.001). (D) DKK1 siRNA (MHCC-97L: p < 0.001 and p < 0.001; HCC-LM3: p <0.001 and p < 0.001), but not CCL14 siRNA (MHCC-97L: p = 0.126 and p = 0.711; HCC-LM3: p = 0.901 and p = 0.694) could attenuate the effect of the CM from HUVEC-AXL-NC and HUVEC-AXL-OE cells on the migration of HCC-LM3 cells and MHCC-97L cells. (E) SOX2 mRNA expression was significantly increased in HUVEC-AXL-OE cells and decreased in HUVEC-AXL-KD cells compared with HUVEC-AXL-NC cells (HUVEC-AXL-KD: p < 0.001, HUVEC-AXL-OE: p < 0.001). (F) AXL overexpression could significantly increase SOX2 and DKK-1 protein expression in HUVEC-AXL-OE cells compared with HUVEC-AXL-NC cells, and SOX2 siRNA inhibited SOX2 and DKK-1 protein expression in HUVEC-AXL-OE and HUVEC-AXL-NC cells.
Article Snippet: The protein concentrations of
Techniques: Ab Array, Expressing, Enzyme-linked Immunosorbent Assay, Migration, Over Expression
Journal: BMC Bioinformatics
Article Title: PAGED: a pathway and gene-set enrichment database to enable molecular phenotype discoveries
doi: 10.1186/1471-2105-13-S15-S2
Figure Lengend Snippet: Top search results of colorectal cancer advanced search
Article Snippet: Protein Lounge suggests "Molecular Mechanisms of Cancer," "Akt Signaling," and other important pathways in colorectal cancer;
Techniques: Clinical Proteomics, Membrane
Journal: International Journal of Stem Cells
Article Title: Upregulation of C-Reactive Protein by Placenta-Derived Mesenchymal Stem Cells Promotes Angiogenesis in A Rat Model with Cirrhotic Liver
doi: 10.15283/ijsc20052
Figure Lengend Snippet: PD-MSC transplantation induces Wnt signaling and angiogene-sis in CCl 4 -injured rats. Angiogenic (A) and Wnt signaling (B) factors were detected by Western blotting. Localization and expression of VEGF and β -catenin visualized using immunofluorescence (C). ×630, Scale bars; 20 μ m. Positive correlations were found between CRP and β -catenin (D) also, between β -catenin and VEGF (E). NTX and TTX refer to the non-transplanted group and the PD-MSC-transplanted group, respec-tively.
Article Snippet: The suppression of the
Techniques: Transplantation Assay, Western Blot, Expressing, Immunofluorescence
Journal: International Journal of Stem Cells
Article Title: Upregulation of C-Reactive Protein by Placenta-Derived Mesenchymal Stem Cells Promotes Angiogenesis in A Rat Model with Cirrhotic Liver
doi: 10.15283/ijsc20052
Figure Lengend Snippet: CRP regulates angiogenesis and Wnt signaling in rat hepatocytes (WB-F344s). Protein levels of CRP (A), VEGF (B), β -catenin (C), ALB (D), HNF1 α (E), and CyclinD1 (F) were evaluated in siRNA-CRP-transfected rat hepatocytes by western blot. Data are represented as the triplicated mean±SD of. *, p<0.05. Mock and si-CRP refer to non-transfected and siRNA-CRP-transfected rat hepatocytes, respectively.
Article Snippet: The suppression of the
Techniques: Transfection, Western Blot
Journal: International Journal of Stem Cells
Article Title: Upregulation of C-Reactive Protein by Placenta-Derived Mesenchymal Stem Cells Promotes Angiogenesis in A Rat Model with Cirrhotic Liver
doi: 10.15283/ijsc20052
Figure Lengend Snippet: PD-MSCs promote the expression of CRP and proliferation of hepatocytes through Wnt signaling. Expression of CRP was analyzed by qRT-PCR (A) and ELISA (B) after CCl 4 treatment and co-culture with PD-MSCs. Immunofluorescence staining shows the localization and expression of BrdU and β -catenin in rat hepatocytes treated with CCl 4 and co-cultured with PD-MSCs (C). ×400, Scale bars; 20 μ m. BrdU- or β -ca-tenin-(D) positive rat hepatocytes were quantified after immunofluore-scence staining. Protein levels of HNF1 α , and CyclinD1 were detected by western blotting in rat hepatocytes treated with CCl 4 and co-cultured with PD-MSCs (E). Intensity of HNF1 α (F) and Cyclin D1 (G) protein bands was calculated. Tripli-cated data are represented as the mean±SD. *, p<0.05.
Article Snippet: The suppression of the
Techniques: Expressing, Quantitative RT-PCR, Enzyme-linked Immunosorbent Assay, Co-Culture Assay, Immunofluorescence, Staining, Cell Culture, Western Blot