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modified boyden chambers 8.0-μm pore membranes  (Corning Life Sciences)

 
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    Corning Life Sciences modified boyden chambers 8.0-μm pore membranes
    Modified Boyden Chambers 8.0 μm Pore Membranes, 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/product/boyden+chamber+system+8%2E0-%CE%BCm/boyden+chambers+8+%CE%BCm+pore+filter/pmc12005444__iovs___66___4___26_s001-30-14-10
    Average 90 stars, based on 1 article reviews
    modified boyden chambers 8.0-μm pore membranes - by Bioz Stars, 2026-10
    90/100 stars

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    Migration:

    Article Title: Wnt5a/ROR1 activates DAAM1 and promotes the migration in osteosarcoma cells.
    Article Snippet: .. A Boyden chamber system (8.0-μm; Costar; Corning, Inc.) was used to perform the cell migration assays. ..



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    Tumor-suppressive role of Biochanin A in CRC in vitro and in vivo. (a) The proliferative capacity of control and Biochanin A-treated CRC cells was examined by CCK-8 assay. (b) The migratory capacity of control and Biochanin A-treated CRC cells was examined by wound healing assay. (c) Quantitative analysis of cell migratory capacity. (d) The invasive capacity of control and Biochanin A-treated CRC cells was examined by <t>Boyden</t> <t>chamber</t> assay. (e) Quantitative analysis of cell invasive capacity. (f) Tumor volume of the mouse models, which was monitored every three days. (g) Isolated tumor images from these two groups on day 21 after the first treatment. (h) The tumor weight of these two groups; mice were sacrificed on day 21 after the first treatment.
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    Image Search Results


    Tumor-suppressive role of Biochanin A in CRC in vitro and in vivo. (a) The proliferative capacity of control and Biochanin A-treated CRC cells was examined by CCK-8 assay. (b) The migratory capacity of control and Biochanin A-treated CRC cells was examined by wound healing assay. (c) Quantitative analysis of cell migratory capacity. (d) The invasive capacity of control and Biochanin A-treated CRC cells was examined by Boyden chamber assay. (e) Quantitative analysis of cell invasive capacity. (f) Tumor volume of the mouse models, which was monitored every three days. (g) Isolated tumor images from these two groups on day 21 after the first treatment. (h) The tumor weight of these two groups; mice were sacrificed on day 21 after the first treatment.

    Journal: Journal of Oncology

    Article Title: Biochanin A Suppresses Tumor Progression and PD-L1 Expression via Inhibiting ZEB1 Expression in Colorectal Cancer

    doi: 10.1155/2022/3224373

    Figure Lengend Snippet: Tumor-suppressive role of Biochanin A in CRC in vitro and in vivo. (a) The proliferative capacity of control and Biochanin A-treated CRC cells was examined by CCK-8 assay. (b) The migratory capacity of control and Biochanin A-treated CRC cells was examined by wound healing assay. (c) Quantitative analysis of cell migratory capacity. (d) The invasive capacity of control and Biochanin A-treated CRC cells was examined by Boyden chamber assay. (e) Quantitative analysis of cell invasive capacity. (f) Tumor volume of the mouse models, which was monitored every three days. (g) Isolated tumor images from these two groups on day 21 after the first treatment. (h) The tumor weight of these two groups; mice were sacrificed on day 21 after the first treatment.

    Article Snippet: For cell invasion assays, 1 × 10 5 cells in serum-free medium supplemented with 5 mg/mL BSA were inoculated to the upper sides of the modified Boyden chamber (8.0- μ m, Cat. 3422, Corning, NY, US).

    Techniques: In Vitro, In Vivo, Control, CCK-8 Assay, Wound Healing Assay, Boyden Chamber Assay, Isolation