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rhoa gtp pulldown assay pak gst  (Cytoskeleton Inc)


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    Cytoskeleton Inc rhoa gtp pulldown assay pak gst
    Rhoa Gtp Pulldown Assay Pak Gst, supplied by Cytoskeleton Inc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rhoa gtp pulldown assay pak gst/product/Cytoskeleton Inc
    Average 94 stars, based on 1 article reviews
    rhoa gtp pulldown assay pak gst - by Bioz Stars, 2025-02
    94/100 stars

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    Effects of TFR on the activation of <t>UTR-RhoA/ROCK</t> pathway in the noninfarcted cardiac area. (a–d) The western blot analysis of U-II receptor (UTR), <t>GTP-RhoA</t> (GTP-binding RhoA), ROCK1, and ROCK2. Data are presented as the mean ± SEM. ∗∗ P < 0.01, compared with the Sham group; # P < 0.05 and ## P < 0.01, compared with the Model group.
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    Cytoskeleton Inc gtp rhoa cdc42 pulldown assays
    Hhex interacted with RHOA and <t>CDC42.</t> a 293FT cells were co-transfected with plasmids of pcDNA3.1 and pcDNA3.1-HHEX-HA or plasmids of pcDNA3.1-HHEX-HA and pcDNA3.1-RHOA-MYC, cell lysate was immunoprecipitated with anti-HA antibody, Hhex and RHOA were detected by western blot. The images are representative of three independent experiments with similar results. b 293FT cells were co-transfected with plasmids of pcDNA3.1 and pcDNA3.1-RHOA-MYC or plasmids of pcDNA3.1-HHEX-HA and pcDNA3.1-RHOA-MYC, cell lysate was immunoprecipitated with anti-MYC antibody, Hhex and RHOA were detected by western blot. The images are representative of three independent experiments with similar results. c 293FT cells were co-transfected with plasmids of pcDNA3.1 and pcDNA3.1-HHEX-HA or plasmids of pcDNA3.1-HHEX-HA and pcDNA3.1-CDC42-MYC, cell lysate was immunoprecipitated with anti-HA antibody, Hhex and CDC42 were detected by western blot. The images are representative of three independent experiments with similar results. d 293FT cells were co-transfected with plasmids of pcDNA3.1 and pcDNA3.1-CDC42-MYC or plasmids of pcDNA3.1-HHEX-HA and pcDNA3.1-RHOA-MYC, cell lysate was immunoprecipitated with anti-MYC antibody, Hhex and CDC42 were detected by western blot. The images are representative of three independent experiments with similar results
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    Hhex interacted with RHOA and <t>CDC42.</t> a 293FT cells were co-transfected with plasmids of pcDNA3.1 and pcDNA3.1-HHEX-HA or plasmids of pcDNA3.1-HHEX-HA and pcDNA3.1-RHOA-MYC, cell lysate was immunoprecipitated with anti-HA antibody, Hhex and RHOA were detected by western blot. The images are representative of three independent experiments with similar results. b 293FT cells were co-transfected with plasmids of pcDNA3.1 and pcDNA3.1-RHOA-MYC or plasmids of pcDNA3.1-HHEX-HA and pcDNA3.1-RHOA-MYC, cell lysate was immunoprecipitated with anti-MYC antibody, Hhex and RHOA were detected by western blot. The images are representative of three independent experiments with similar results. c 293FT cells were co-transfected with plasmids of pcDNA3.1 and pcDNA3.1-HHEX-HA or plasmids of pcDNA3.1-HHEX-HA and pcDNA3.1-CDC42-MYC, cell lysate was immunoprecipitated with anti-HA antibody, Hhex and CDC42 were detected by western blot. The images are representative of three independent experiments with similar results. d 293FT cells were co-transfected with plasmids of pcDNA3.1 and pcDNA3.1-CDC42-MYC or plasmids of pcDNA3.1-HHEX-HA and pcDNA3.1-RHOA-MYC, cell lysate was immunoprecipitated with anti-MYC antibody, Hhex and CDC42 were detected by western blot. The images are representative of three independent experiments with similar results
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    Hhex interacted with RHOA and <t>CDC42.</t> a 293FT cells were co-transfected with plasmids of pcDNA3.1 and pcDNA3.1-HHEX-HA or plasmids of pcDNA3.1-HHEX-HA and pcDNA3.1-RHOA-MYC, cell lysate was immunoprecipitated with anti-HA antibody, Hhex and RHOA were detected by western blot. The images are representative of three independent experiments with similar results. b 293FT cells were co-transfected with plasmids of pcDNA3.1 and pcDNA3.1-RHOA-MYC or plasmids of pcDNA3.1-HHEX-HA and pcDNA3.1-RHOA-MYC, cell lysate was immunoprecipitated with anti-MYC antibody, Hhex and RHOA were detected by western blot. The images are representative of three independent experiments with similar results. c 293FT cells were co-transfected with plasmids of pcDNA3.1 and pcDNA3.1-HHEX-HA or plasmids of pcDNA3.1-HHEX-HA and pcDNA3.1-CDC42-MYC, cell lysate was immunoprecipitated with anti-HA antibody, Hhex and CDC42 were detected by western blot. The images are representative of three independent experiments with similar results. d 293FT cells were co-transfected with plasmids of pcDNA3.1 and pcDNA3.1-CDC42-MYC or plasmids of pcDNA3.1-HHEX-HA and pcDNA3.1-RHOA-MYC, cell lysate was immunoprecipitated with anti-MYC antibody, Hhex and CDC42 were detected by western blot. The images are representative of three independent experiments with similar results
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    https://www.bioz.com/result/rac1 gtp pulldown assay/product/Cytoskeleton Inc
    Average 94 stars, based on 1 article reviews
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    Image Search Results


    Effects of TFR on the activation of UTR-RhoA/ROCK pathway in the noninfarcted cardiac area. (a–d) The western blot analysis of U-II receptor (UTR), GTP-RhoA (GTP-binding RhoA), ROCK1, and ROCK2. Data are presented as the mean ± SEM. ∗∗ P < 0.01, compared with the Sham group; # P < 0.05 and ## P < 0.01, compared with the Model group.

    Journal: Evidence-based Complementary and Alternative Medicine : eCAM

    Article Title: Effects of Total Flavone from Rhododendron simsii Planch. Flower on Postischemic Cardiac Dysfunction and Cardiac Remodeling in Rats

    doi: 10.1155/2017/5389272

    Figure Lengend Snippet: Effects of TFR on the activation of UTR-RhoA/ROCK pathway in the noninfarcted cardiac area. (a–d) The western blot analysis of U-II receptor (UTR), GTP-RhoA (GTP-binding RhoA), ROCK1, and ROCK2. Data are presented as the mean ± SEM. ∗∗ P < 0.01, compared with the Sham group; # P < 0.05 and ## P < 0.01, compared with the Model group.

    Article Snippet: GTP-RhoA was assessed by using commercially available kits from Cytoskeleton (BK 036-S) following the manufacturer's instructions.

    Techniques: Activation Assay, Western Blot, Binding Assay

    Hhex interacted with RHOA and CDC42. a 293FT cells were co-transfected with plasmids of pcDNA3.1 and pcDNA3.1-HHEX-HA or plasmids of pcDNA3.1-HHEX-HA and pcDNA3.1-RHOA-MYC, cell lysate was immunoprecipitated with anti-HA antibody, Hhex and RHOA were detected by western blot. The images are representative of three independent experiments with similar results. b 293FT cells were co-transfected with plasmids of pcDNA3.1 and pcDNA3.1-RHOA-MYC or plasmids of pcDNA3.1-HHEX-HA and pcDNA3.1-RHOA-MYC, cell lysate was immunoprecipitated with anti-MYC antibody, Hhex and RHOA were detected by western blot. The images are representative of three independent experiments with similar results. c 293FT cells were co-transfected with plasmids of pcDNA3.1 and pcDNA3.1-HHEX-HA or plasmids of pcDNA3.1-HHEX-HA and pcDNA3.1-CDC42-MYC, cell lysate was immunoprecipitated with anti-HA antibody, Hhex and CDC42 were detected by western blot. The images are representative of three independent experiments with similar results. d 293FT cells were co-transfected with plasmids of pcDNA3.1 and pcDNA3.1-CDC42-MYC or plasmids of pcDNA3.1-HHEX-HA and pcDNA3.1-RHOA-MYC, cell lysate was immunoprecipitated with anti-MYC antibody, Hhex and CDC42 were detected by western blot. The images are representative of three independent experiments with similar results

    Journal: Cell Communication and Signaling : CCS

    Article Title: Hhex inhibits cell migration via regulating RHOA/CDC42-CFL1 axis in human lung cancer cells

    doi: 10.1186/s12964-021-00763-6

    Figure Lengend Snippet: Hhex interacted with RHOA and CDC42. a 293FT cells were co-transfected with plasmids of pcDNA3.1 and pcDNA3.1-HHEX-HA or plasmids of pcDNA3.1-HHEX-HA and pcDNA3.1-RHOA-MYC, cell lysate was immunoprecipitated with anti-HA antibody, Hhex and RHOA were detected by western blot. The images are representative of three independent experiments with similar results. b 293FT cells were co-transfected with plasmids of pcDNA3.1 and pcDNA3.1-RHOA-MYC or plasmids of pcDNA3.1-HHEX-HA and pcDNA3.1-RHOA-MYC, cell lysate was immunoprecipitated with anti-MYC antibody, Hhex and RHOA were detected by western blot. The images are representative of three independent experiments with similar results. c 293FT cells were co-transfected with plasmids of pcDNA3.1 and pcDNA3.1-HHEX-HA or plasmids of pcDNA3.1-HHEX-HA and pcDNA3.1-CDC42-MYC, cell lysate was immunoprecipitated with anti-HA antibody, Hhex and CDC42 were detected by western blot. The images are representative of three independent experiments with similar results. d 293FT cells were co-transfected with plasmids of pcDNA3.1 and pcDNA3.1-CDC42-MYC or plasmids of pcDNA3.1-HHEX-HA and pcDNA3.1-RHOA-MYC, cell lysate was immunoprecipitated with anti-MYC antibody, Hhex and CDC42 were detected by western blot. The images are representative of three independent experiments with similar results

    Article Snippet: GTP–RhoA/CDC42 pulldown assays were performed with RhoA/CDC42 Pulldown Activation Assay Kit (Cytoskeleton) according to the manufacturer’s instructions.

    Techniques: Transfection, Immunoprecipitation, Western Blot

    Hhex inhibited RHOA and CDC42 activation. a pcDNA3.1 or pcDNA3.1-HHEX plasmid was transfected into A549 cells and H1299 cells for 24 h. RHOA activation assay kit was used for detecting RHOA-GTP active form. The kit supplies His-RHOA protein as a control. b H1299 cells were transfected with pcDNA3.1 or pcDNA3.1-HHEX plasmid respectively for 24 h. Then, active CDC42-GTP level was tested by CDC42 activation assay kit. c Hhex was knocked down in A549 cells, RHOA-GTP assay was conducted. d Hhex was knocked down in A549 cells, CDC42-GTP assay was performed. Results are from one representative experiment of at least three

    Journal: Cell Communication and Signaling : CCS

    Article Title: Hhex inhibits cell migration via regulating RHOA/CDC42-CFL1 axis in human lung cancer cells

    doi: 10.1186/s12964-021-00763-6

    Figure Lengend Snippet: Hhex inhibited RHOA and CDC42 activation. a pcDNA3.1 or pcDNA3.1-HHEX plasmid was transfected into A549 cells and H1299 cells for 24 h. RHOA activation assay kit was used for detecting RHOA-GTP active form. The kit supplies His-RHOA protein as a control. b H1299 cells were transfected with pcDNA3.1 or pcDNA3.1-HHEX plasmid respectively for 24 h. Then, active CDC42-GTP level was tested by CDC42 activation assay kit. c Hhex was knocked down in A549 cells, RHOA-GTP assay was conducted. d Hhex was knocked down in A549 cells, CDC42-GTP assay was performed. Results are from one representative experiment of at least three

    Article Snippet: GTP–RhoA/CDC42 pulldown assays were performed with RhoA/CDC42 Pulldown Activation Assay Kit (Cytoskeleton) according to the manufacturer’s instructions.

    Techniques: Activation Assay, Plasmid Preparation, Transfection

    Hhex enhanced interaction of RHOGDIA with RHOA/CDC42. a HHEX siRNA-RHOGDIA were co-transfected into A549. Cell lysate was immunoprecipitated with anti-FLAG antibody, Hhex, RHOA were detected by western blot. The images are representative of three independent experiments with similar results. b HHEX siRNA and pcDNA3.1-RHOGDIA were co-transfected into Calu-1. Cell lysate was immunoprecipitated with anti-FLAG antibody, Hhex, RHOA were detected by western blot. The images are representative of three independent experiments with similar results. c A549 cells were conducted same treatments as ( a ), Hhex and CDC42 were detected by western blot. The images are representative of three independent experiments with similar results. d Calu-1 cells were conducted same treatments as ( a ), Hhex and CDC42 were detected by western blot. The images are representative of three independent experiments with similar results

    Journal: Cell Communication and Signaling : CCS

    Article Title: Hhex inhibits cell migration via regulating RHOA/CDC42-CFL1 axis in human lung cancer cells

    doi: 10.1186/s12964-021-00763-6

    Figure Lengend Snippet: Hhex enhanced interaction of RHOGDIA with RHOA/CDC42. a HHEX siRNA-RHOGDIA were co-transfected into A549. Cell lysate was immunoprecipitated with anti-FLAG antibody, Hhex, RHOA were detected by western blot. The images are representative of three independent experiments with similar results. b HHEX siRNA and pcDNA3.1-RHOGDIA were co-transfected into Calu-1. Cell lysate was immunoprecipitated with anti-FLAG antibody, Hhex, RHOA were detected by western blot. The images are representative of three independent experiments with similar results. c A549 cells were conducted same treatments as ( a ), Hhex and CDC42 were detected by western blot. The images are representative of three independent experiments with similar results. d Calu-1 cells were conducted same treatments as ( a ), Hhex and CDC42 were detected by western blot. The images are representative of three independent experiments with similar results

    Article Snippet: GTP–RhoA/CDC42 pulldown assays were performed with RhoA/CDC42 Pulldown Activation Assay Kit (Cytoskeleton) according to the manufacturer’s instructions.

    Techniques: Transfection, Immunoprecipitation, Western Blot