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bftc909 cells  (Guangzhou JET Bio-Filtration)


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    Structured Review

    Guangzhou JET Bio-Filtration bftc909 cells
    BOC silencing suppresses cell migration in urothelial carcinoma cells. ( A ) qRT-PCR confirmed efficient knockdown of BOC expression in <t>BFTC909</t> cells using two independent shRNAs (**, p < 0.01, one-way ANOVA). ( B–D ) Representative images and quantification of Boyden chamber assays demonstrated significantly decreased migration in shBOC cells compared with controls (***, p < 0.001, one-way ANOVA). Scale bar: 200 µm, ( E,F ) RTCA migration assays showed impaired migration of BFTC909 cells after BOC knockdown (***, p < 0.001, two-way ANOVA with repeated measures and post-hoc tests).
    Bftc909 Cells, supplied by Guangzhou JET Bio-Filtration, used in various techniques. Bioz Stars score: 99/100, based on 90 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/inserts/pmc13040342-90-7-21?v=Guangzhou+JET+Bio-Filtration
    Average 99 stars, based on 90 article reviews
    bftc909 cells - by Bioz Stars, 2026-08
    99/100 stars

    Images

    1) Product Images from "Pre-Treatment BOC Expression as an Indicator of Lymphovascular Invasion and In Vitro Chemotherapeutic Response in Upper Tract Urothelial Carcinoma"

    Article Title: Pre-Treatment BOC Expression as an Indicator of Lymphovascular Invasion and In Vitro Chemotherapeutic Response in Upper Tract Urothelial Carcinoma

    Journal: Oncology Research

    doi: 10.32604/or.2026.070837

    BOC silencing suppresses cell migration in urothelial carcinoma cells. ( A ) qRT-PCR confirmed efficient knockdown of BOC expression in BFTC909 cells using two independent shRNAs (**, p < 0.01, one-way ANOVA). ( B–D ) Representative images and quantification of Boyden chamber assays demonstrated significantly decreased migration in shBOC cells compared with controls (***, p < 0.001, one-way ANOVA). Scale bar: 200 µm, ( E,F ) RTCA migration assays showed impaired migration of BFTC909 cells after BOC knockdown (***, p < 0.001, two-way ANOVA with repeated measures and post-hoc tests).
    Figure Legend Snippet: BOC silencing suppresses cell migration in urothelial carcinoma cells. ( A ) qRT-PCR confirmed efficient knockdown of BOC expression in BFTC909 cells using two independent shRNAs (**, p < 0.01, one-way ANOVA). ( B–D ) Representative images and quantification of Boyden chamber assays demonstrated significantly decreased migration in shBOC cells compared with controls (***, p < 0.001, one-way ANOVA). Scale bar: 200 µm, ( E,F ) RTCA migration assays showed impaired migration of BFTC909 cells after BOC knockdown (***, p < 0.001, two-way ANOVA with repeated measures and post-hoc tests).

    Techniques Used: Migration, Quantitative RT-PCR, Knockdown, Expressing

    BOC silencing enhances sensitivity to cisplatin and gemcitabine in BFTC909 cells. ( A – D ) Cell viability assays were performed in BFTC909 cells with BOC knockdown (shBOC#1) or control (shScramble) following treatment with ( A ) cisplatin, ( B ) gemcitabine, ( C ) paclitaxel, or ( D ) epirubicin at the indicated concentrations. Data are presented as mean ± SEM. All statistics were determined using the one-way ANOVA. **, p < 0.01; ***, p < 0.001; ns, not significant.
    Figure Legend Snippet: BOC silencing enhances sensitivity to cisplatin and gemcitabine in BFTC909 cells. ( A – D ) Cell viability assays were performed in BFTC909 cells with BOC knockdown (shBOC#1) or control (shScramble) following treatment with ( A ) cisplatin, ( B ) gemcitabine, ( C ) paclitaxel, or ( D ) epirubicin at the indicated concentrations. Data are presented as mean ± SEM. All statistics were determined using the one-way ANOVA. **, p < 0.01; ***, p < 0.001; ns, not significant.

    Techniques Used: Knockdown, Control



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    Image Search Results


    Evaluation of angiogenic potential induced by Mg 2+ and NRP-1. ( A ) Scratch assay in three different microenvironments. ( B ) Transwell assay in three different microenvironments. ( C ) Quantitative analysis of wound healing area. ( D ) Quantitative analysis of number of migration cells. ( E ) Immunofluorescence staining of VEGFA and FGF2, with DAPI for nuclear staining and F-actin for cytoskeleton labeling. ( F ) Tube formation evaluation in four different microenvironments. ( G ) Quantitative analysis of number of junction. ( H ) Quantitative analysis of Flu intensity. ( I ) Western-blot analysis of VEGFA, FGF2, and Nr4a1. ( J-L ) Quantitative analysis of relative protein expression of VEGFA, FGF2, and Nr4a1. Data are presented as mean values ± s.d. (n = 3). ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001 (one-way ANOVA).

    Journal: Bioactive Materials

    Article Title: Reconstructing the ischemic osteogenic microenvironment through hierarchical scaffolds orchestrating Mg 2+ signaling and neuropilin-1–mediated angiogenesis

    doi: 10.1016/j.bioactmat.2026.02.031

    Figure Lengend Snippet: Evaluation of angiogenic potential induced by Mg 2+ and NRP-1. ( A ) Scratch assay in three different microenvironments. ( B ) Transwell assay in three different microenvironments. ( C ) Quantitative analysis of wound healing area. ( D ) Quantitative analysis of number of migration cells. ( E ) Immunofluorescence staining of VEGFA and FGF2, with DAPI for nuclear staining and F-actin for cytoskeleton labeling. ( F ) Tube formation evaluation in four different microenvironments. ( G ) Quantitative analysis of number of junction. ( H ) Quantitative analysis of Flu intensity. ( I ) Western-blot analysis of VEGFA, FGF2, and Nr4a1. ( J-L ) Quantitative analysis of relative protein expression of VEGFA, FGF2, and Nr4a1. Data are presented as mean values ± s.d. (n = 3). ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001 (one-way ANOVA).

    Article Snippet: For the Transwell assay, BMSCs were seeded in the upper chambers of Transwell inserts (8.0 μm pore size; Servicebio, China), while different culture conditions were applied in the lower chambers according to the experimental groups.

    Techniques: Wound Healing Assay, Transwell Assay, Migration, Immunofluorescence, Staining, Labeling, Western Blot, Expressing