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troap rabbit mab  (Proteintech)


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    Structured Review

    Proteintech troap rabbit mab
    GSEA enrichment analysis of <t>TROAP</t> using the GEO database. (A, B) KEGG pathways were screened with the Fold change value greater than 0 and p < 0.05 as screening conditions. The dotplot showed the 19 upregulated (NES > 0) and 4 downregulated (NES < 0) pathways. (C) GSEA enrichment plots represented that enrichment <t>of</t> <t>Wnt/β‐Catenin</t> pathway. (D, E) Immunofluorescence showing overexpression of TROAP increased level of Axin2 protein in the cytoplasm of TJ905 cells compared to control, meanwhile, TROAP overexpression also upregulated the accumulation of β‐Catenin in the cytoplasm and nucleus of TJ905 cells compared to control. Immunofluorescence quantification analysis was shown in E. (F, G) Immunofluorescence assay on U251 cells transfected with TROAP siRNA (* p < 0.05, ** p < 0.01, *** p < 0.001, respectively)
    Troap Rabbit Mab, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/troap+rabbit+mab/pmc08339535-64-9-12?v=Proteintech
    Average 93 stars, based on 9 article reviews
    troap rabbit mab - by Bioz Stars, 2026-07
    93/100 stars

    Images

    1) Product Images from "TROAP regulates cell cycle and promotes tumor progression through Wnt/β‐Catenin signaling pathway in glioma cells"

    Article Title: TROAP regulates cell cycle and promotes tumor progression through Wnt/β‐Catenin signaling pathway in glioma cells

    Journal: CNS Neuroscience & Therapeutics

    doi: 10.1111/cns.13688

    GSEA enrichment analysis of TROAP using the GEO database. (A, B) KEGG pathways were screened with the Fold change value greater than 0 and p < 0.05 as screening conditions. The dotplot showed the 19 upregulated (NES > 0) and 4 downregulated (NES < 0) pathways. (C) GSEA enrichment plots represented that enrichment of Wnt/β‐Catenin pathway. (D, E) Immunofluorescence showing overexpression of TROAP increased level of Axin2 protein in the cytoplasm of TJ905 cells compared to control, meanwhile, TROAP overexpression also upregulated the accumulation of β‐Catenin in the cytoplasm and nucleus of TJ905 cells compared to control. Immunofluorescence quantification analysis was shown in E. (F, G) Immunofluorescence assay on U251 cells transfected with TROAP siRNA (* p < 0.05, ** p < 0.01, *** p < 0.001, respectively)
    Figure Legend Snippet: GSEA enrichment analysis of TROAP using the GEO database. (A, B) KEGG pathways were screened with the Fold change value greater than 0 and p < 0.05 as screening conditions. The dotplot showed the 19 upregulated (NES > 0) and 4 downregulated (NES < 0) pathways. (C) GSEA enrichment plots represented that enrichment of Wnt/β‐Catenin pathway. (D, E) Immunofluorescence showing overexpression of TROAP increased level of Axin2 protein in the cytoplasm of TJ905 cells compared to control, meanwhile, TROAP overexpression also upregulated the accumulation of β‐Catenin in the cytoplasm and nucleus of TJ905 cells compared to control. Immunofluorescence quantification analysis was shown in E. (F, G) Immunofluorescence assay on U251 cells transfected with TROAP siRNA (* p < 0.05, ** p < 0.01, *** p < 0.001, respectively)

    Techniques Used: Immunofluorescence, Over Expression, Control, Transfection

    TROAP‐induced malignant phenotype via activating the Wnt/β‐Catenin signaling in glioma cells. (A, B) Western blot analysis showing the expression of Wnt/β‐Catenin signaling‐related proteins after silencing Axin2 or β‐Catenin in TJ905 cells ectopically overexpressing TROAP. The statistics were shown in the histogram C and D. The effect of TROAP overexpression on cell proliferation(E‐H), migration and invasion (I, J) was partly eliminated by silencing Axin2 or β‐Catenin (* p < 0.05, ** p < 0.01, *** p < 0.001, respectively)
    Figure Legend Snippet: TROAP‐induced malignant phenotype via activating the Wnt/β‐Catenin signaling in glioma cells. (A, B) Western blot analysis showing the expression of Wnt/β‐Catenin signaling‐related proteins after silencing Axin2 or β‐Catenin in TJ905 cells ectopically overexpressing TROAP. The statistics were shown in the histogram C and D. The effect of TROAP overexpression on cell proliferation(E‐H), migration and invasion (I, J) was partly eliminated by silencing Axin2 or β‐Catenin (* p < 0.05, ** p < 0.01, *** p < 0.001, respectively)

    Techniques Used: Western Blot, Expressing, Over Expression, Migration



    Similar Products

    troap rabbit mab  (Proteintech)
    93
    Proteintech troap rabbit mab
    GSEA enrichment analysis of <t>TROAP</t> using the GEO database. (A, B) KEGG pathways were screened with the Fold change value greater than 0 and p < 0.05 as screening conditions. The dotplot showed the 19 upregulated (NES > 0) and 4 downregulated (NES < 0) pathways. (C) GSEA enrichment plots represented that enrichment <t>of</t> <t>Wnt/β‐Catenin</t> pathway. (D, E) Immunofluorescence showing overexpression of TROAP increased level of Axin2 protein in the cytoplasm of TJ905 cells compared to control, meanwhile, TROAP overexpression also upregulated the accumulation of β‐Catenin in the cytoplasm and nucleus of TJ905 cells compared to control. Immunofluorescence quantification analysis was shown in E. (F, G) Immunofluorescence assay on U251 cells transfected with TROAP siRNA (* p < 0.05, ** p < 0.01, *** p < 0.001, respectively)
    Troap Rabbit Mab, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/troap+rabbit+mab/pmc08339535-64-9-12?v=Proteintech
    Average 93 stars, based on 1 article reviews
    troap rabbit mab - by Bioz Stars, 2026-07
    93/100 stars
    		  Buy from Supplier

    Image Search Results


    GSEA enrichment analysis of TROAP using the GEO database. (A, B) KEGG pathways were screened with the Fold change value greater than 0 and p < 0.05 as screening conditions. The dotplot showed the 19 upregulated (NES > 0) and 4 downregulated (NES < 0) pathways. (C) GSEA enrichment plots represented that enrichment of Wnt/β‐Catenin pathway. (D, E) Immunofluorescence showing overexpression of TROAP increased level of Axin2 protein in the cytoplasm of TJ905 cells compared to control, meanwhile, TROAP overexpression also upregulated the accumulation of β‐Catenin in the cytoplasm and nucleus of TJ905 cells compared to control. Immunofluorescence quantification analysis was shown in E. (F, G) Immunofluorescence assay on U251 cells transfected with TROAP siRNA (* p < 0.05, ** p < 0.01, *** p < 0.001, respectively)

    Journal: CNS Neuroscience & Therapeutics

    Article Title: TROAP regulates cell cycle and promotes tumor progression through Wnt/β‐Catenin signaling pathway in glioma cells

    doi: 10.1111/cns.13688

    Figure Lengend Snippet: GSEA enrichment analysis of TROAP using the GEO database. (A, B) KEGG pathways were screened with the Fold change value greater than 0 and p < 0.05 as screening conditions. The dotplot showed the 19 upregulated (NES > 0) and 4 downregulated (NES < 0) pathways. (C) GSEA enrichment plots represented that enrichment of Wnt/β‐Catenin pathway. (D, E) Immunofluorescence showing overexpression of TROAP increased level of Axin2 protein in the cytoplasm of TJ905 cells compared to control, meanwhile, TROAP overexpression also upregulated the accumulation of β‐Catenin in the cytoplasm and nucleus of TJ905 cells compared to control. Immunofluorescence quantification analysis was shown in E. (F, G) Immunofluorescence assay on U251 cells transfected with TROAP siRNA (* p < 0.05, ** p < 0.01, *** p < 0.001, respectively)

    Article Snippet: Western blot analysis was performed by the following antibodies: TROAP rabbit mAb (Proteintech, 13634‐1‐AP, 1:2000), β‐catenin rabbit mAb (No.66379‐1‐Ig, 1:4000), MMP‐7 rabbit mAb (No.1 0374‐2‐AP, 1:3000), CDK2 rabbit mAb (No.10122‐1‐AP, 1:800), CDK4 rabbit mAb (No.11026‐1‐AP, 1:3000), Axin2 rabbit mAb(No. ET1703‐96; WB 1:3000), MMP‐2 rabbit mAb (No.10373‐2‐AP, 1:3000), RHOA rabbit mAb (No.10749–1‐AP, 1:2000), ROCK1 rabbit mAb (No.21850‐1‐AP, 1:2000), GAPDH mouse mAb(No.60004‐1‐Ig, 1:3000).

    Techniques: Immunofluorescence, Over Expression, Control, Transfection

    TROAP‐induced malignant phenotype via activating the Wnt/β‐Catenin signaling in glioma cells. (A, B) Western blot analysis showing the expression of Wnt/β‐Catenin signaling‐related proteins after silencing Axin2 or β‐Catenin in TJ905 cells ectopically overexpressing TROAP. The statistics were shown in the histogram C and D. The effect of TROAP overexpression on cell proliferation(E‐H), migration and invasion (I, J) was partly eliminated by silencing Axin2 or β‐Catenin (* p < 0.05, ** p < 0.01, *** p < 0.001, respectively)

    Journal: CNS Neuroscience & Therapeutics

    Article Title: TROAP regulates cell cycle and promotes tumor progression through Wnt/β‐Catenin signaling pathway in glioma cells

    doi: 10.1111/cns.13688

    Figure Lengend Snippet: TROAP‐induced malignant phenotype via activating the Wnt/β‐Catenin signaling in glioma cells. (A, B) Western blot analysis showing the expression of Wnt/β‐Catenin signaling‐related proteins after silencing Axin2 or β‐Catenin in TJ905 cells ectopically overexpressing TROAP. The statistics were shown in the histogram C and D. The effect of TROAP overexpression on cell proliferation(E‐H), migration and invasion (I, J) was partly eliminated by silencing Axin2 or β‐Catenin (* p < 0.05, ** p < 0.01, *** p < 0.001, respectively)

    Article Snippet: Western blot analysis was performed by the following antibodies: TROAP rabbit mAb (Proteintech, 13634‐1‐AP, 1:2000), β‐catenin rabbit mAb (No.66379‐1‐Ig, 1:4000), MMP‐7 rabbit mAb (No.1 0374‐2‐AP, 1:3000), CDK2 rabbit mAb (No.10122‐1‐AP, 1:800), CDK4 rabbit mAb (No.11026‐1‐AP, 1:3000), Axin2 rabbit mAb(No. ET1703‐96; WB 1:3000), MMP‐2 rabbit mAb (No.10373‐2‐AP, 1:3000), RHOA rabbit mAb (No.10749–1‐AP, 1:2000), ROCK1 rabbit mAb (No.21850‐1‐AP, 1:2000), GAPDH mouse mAb(No.60004‐1‐Ig, 1:3000).

    Techniques: Western Blot, Expressing, Over Expression, Migration