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modified boyden chamber ( pore size falcon® transwell inserts)  (Corning Life Sciences)

 
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    Corning Life Sciences modified boyden chamber ( pore size falcon® transwell inserts)
    CtBP2 favors cell migration. A Representative images of K7M2 cell migration after 10 h incubation, as assessed by <t>Boyden</t> <t>chamber</t> assay. CtBP2-silenced K7M2 cells were stained in green, and CtBP2-overexpressing cells were stained in red before seeding (bar = 100 µm). B Estimation plot representing the relative number of migrating cells. The difference between the group means is represented on the right. C Representative images of cell migration (wound healing assay) taken at time 18 h after the wound. Control and CtBP2-silenced K7M2 cells were incubated in the presence or absence of recombinant CYR61 (1 µg/mL). The dotted rectangles outline the initial wound surface. D Quantitative evaluation of the cell migration rate. Results are expressed as box plot ( n = 15–22). An asterisk (*) indicates a statistically significant difference ( p < 0.05 vs. Control)
    Modified Boyden Chamber ( Pore Size Falcon® Transwell Inserts), supplied by Corning Life Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/modified boyden chamber ( pore size falcon® transwell inserts)/product/Corning Life Sciences
    Average 90 stars, based on 1 article reviews
    modified boyden chamber ( pore size falcon® transwell inserts) - by Bioz Stars, 2026-05
    90/100 stars

    Images

    1) Product Images from "C-terminal binding protein-2 triggers CYR61-induced metastatic dissemination of osteosarcoma in a non-hypoxic microenvironment"

    Article Title: C-terminal binding protein-2 triggers CYR61-induced metastatic dissemination of osteosarcoma in a non-hypoxic microenvironment

    Journal: Journal of Experimental & Clinical Cancer Research : CR

    doi: 10.1186/s13046-025-03350-6

    CtBP2 favors cell migration. A Representative images of K7M2 cell migration after 10 h incubation, as assessed by Boyden chamber assay. CtBP2-silenced K7M2 cells were stained in green, and CtBP2-overexpressing cells were stained in red before seeding (bar = 100 µm). B Estimation plot representing the relative number of migrating cells. The difference between the group means is represented on the right. C Representative images of cell migration (wound healing assay) taken at time 18 h after the wound. Control and CtBP2-silenced K7M2 cells were incubated in the presence or absence of recombinant CYR61 (1 µg/mL). The dotted rectangles outline the initial wound surface. D Quantitative evaluation of the cell migration rate. Results are expressed as box plot ( n = 15–22). An asterisk (*) indicates a statistically significant difference ( p < 0.05 vs. Control)
    Figure Legend Snippet: CtBP2 favors cell migration. A Representative images of K7M2 cell migration after 10 h incubation, as assessed by Boyden chamber assay. CtBP2-silenced K7M2 cells were stained in green, and CtBP2-overexpressing cells were stained in red before seeding (bar = 100 µm). B Estimation plot representing the relative number of migrating cells. The difference between the group means is represented on the right. C Representative images of cell migration (wound healing assay) taken at time 18 h after the wound. Control and CtBP2-silenced K7M2 cells were incubated in the presence or absence of recombinant CYR61 (1 µg/mL). The dotted rectangles outline the initial wound surface. D Quantitative evaluation of the cell migration rate. Results are expressed as box plot ( n = 15–22). An asterisk (*) indicates a statistically significant difference ( p < 0.05 vs. Control)

    Techniques Used: Migration, Incubation, Boyden Chamber Assay, Staining, Wound Healing Assay, Control, Recombinant



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    CtBP2 favors cell migration. A Representative images of K7M2 cell migration after 10 h incubation, as assessed by <t>Boyden</t> <t>chamber</t> assay. CtBP2-silenced K7M2 cells were stained in green, and CtBP2-overexpressing cells were stained in red before seeding (bar = 100 µm). B Estimation plot representing the relative number of migrating cells. The difference between the group means is represented on the right. C Representative images of cell migration (wound healing assay) taken at time 18 h after the wound. Control and CtBP2-silenced K7M2 cells were incubated in the presence or absence of recombinant CYR61 (1 µg/mL). The dotted rectangles outline the initial wound surface. D Quantitative evaluation of the cell migration rate. Results are expressed as box plot ( n = 15–22). An asterisk (*) indicates a statistically significant difference ( p < 0.05 vs. Control)
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    Image Search Results


    CtBP2 favors cell migration. A Representative images of K7M2 cell migration after 10 h incubation, as assessed by Boyden chamber assay. CtBP2-silenced K7M2 cells were stained in green, and CtBP2-overexpressing cells were stained in red before seeding (bar = 100 µm). B Estimation plot representing the relative number of migrating cells. The difference between the group means is represented on the right. C Representative images of cell migration (wound healing assay) taken at time 18 h after the wound. Control and CtBP2-silenced K7M2 cells were incubated in the presence or absence of recombinant CYR61 (1 µg/mL). The dotted rectangles outline the initial wound surface. D Quantitative evaluation of the cell migration rate. Results are expressed as box plot ( n = 15–22). An asterisk (*) indicates a statistically significant difference ( p < 0.05 vs. Control)

    Journal: Journal of Experimental & Clinical Cancer Research : CR

    Article Title: C-terminal binding protein-2 triggers CYR61-induced metastatic dissemination of osteosarcoma in a non-hypoxic microenvironment

    doi: 10.1186/s13046-025-03350-6

    Figure Lengend Snippet: CtBP2 favors cell migration. A Representative images of K7M2 cell migration after 10 h incubation, as assessed by Boyden chamber assay. CtBP2-silenced K7M2 cells were stained in green, and CtBP2-overexpressing cells were stained in red before seeding (bar = 100 µm). B Estimation plot representing the relative number of migrating cells. The difference between the group means is represented on the right. C Representative images of cell migration (wound healing assay) taken at time 18 h after the wound. Control and CtBP2-silenced K7M2 cells were incubated in the presence or absence of recombinant CYR61 (1 µg/mL). The dotted rectangles outline the initial wound surface. D Quantitative evaluation of the cell migration rate. Results are expressed as box plot ( n = 15–22). An asterisk (*) indicates a statistically significant difference ( p < 0.05 vs. Control)

    Article Snippet: The cell migration rate was evaluated using modified Boyden chamber (8 μm pore size Falcon® Transwell inserts, Corning, Boulogne-Billancourt, France).

    Techniques: Migration, Incubation, Boyden Chamber Assay, Staining, Wound Healing Assay, Control, Recombinant

    VERU-111 suppresses migration and invasion of ovarian cancer cells. Effect of VERU-111 on migration (A) or invasion (B) of ovarian cancer cells using modified transwell chambers in 24-well plates. Cells were treated with vehicle or 20 nM VERU-111 for 48 or 24 hours, respectively. Representative images of control and treatment groups were captured at 20× magnification. All data are presented as the grand mean ± SEM of stained cells from at least 3 different fields. ∗∗ P < .01, ∗∗∗ P < .001, n.s., not significant.

    Journal: The Journal of Pharmacology and Experimental Therapeutics

    Article Title: VERU-111, an orally available tubulin inhibitor, suppresses ovarian tumor growth and metastasis

    doi: 10.1124/jpet.124.002298

    Figure Lengend Snippet: VERU-111 suppresses migration and invasion of ovarian cancer cells. Effect of VERU-111 on migration (A) or invasion (B) of ovarian cancer cells using modified transwell chambers in 24-well plates. Cells were treated with vehicle or 20 nM VERU-111 for 48 or 24 hours, respectively. Representative images of control and treatment groups were captured at 20× magnification. All data are presented as the grand mean ± SEM of stained cells from at least 3 different fields. ∗∗ P < .01, ∗∗∗ P < .001, n.s., not significant.

    Article Snippet: For migration assays, SKOV3 or OVCAR3 cells (3 × 10 4 ) were treated with vehicle or 20 nM VERU-111, suspended in 300 μ L serum-free RPMI 1640 medium, and added to the upper chamber of a modified transwell chamber (BD Falcon) inserted in a 24-well plate.

    Techniques: Migration, Modification, Control, Staining