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human umbilical vein endothelial fusion cells  (ATCC)


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    ATCC human umbilical vein endothelial fusion cells
    Representative images of ( A ) H&E staining and ( B–D ) immunofluorescence (IFS) staining of vascular cross-sections of rat carotid arteries after 10 months of implantation. (B) IFS staining of macrophage marker CD68 (pink). (C) IFS staining of <t>endothelial</t> marker CD31 (green) and contractile smooth muscle marker α-SMA (red). (D) IFS staining of contractile phenotypic smooth muscle cell marker α-SMA (red) and active proliferating cell marker Ki67 (green). W = wires; A = new vessel in neointima; the right column shows the magnified images of the yellow rectangular box in the corresponding left column of images.
    Human Umbilical Vein Endothelial Fusion Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 4946 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+umbilical+vein+endothelial+fusion+cells/Primary+Umbilical+Vein+Endothelial+Cells%3B+Normal%2C+Human/pmc13020250-37-0-8
    Average 99 stars, based on 4946 article reviews
    human umbilical vein endothelial fusion cells - by Bioz Stars, 2026-09
    99/100 stars

    Images

    1) Product Images from "Zn ion-implanted absorbable Fe for improved cytocompatibility and mitigated neointimal hyperplasia"

    Article Title: Zn ion-implanted absorbable Fe for improved cytocompatibility and mitigated neointimal hyperplasia

    Journal: Regenerative Biomaterials

    doi: 10.1093/rb/rbaf112

    Representative images of ( A ) H&E staining and ( B–D ) immunofluorescence (IFS) staining of vascular cross-sections of rat carotid arteries after 10 months of implantation. (B) IFS staining of macrophage marker CD68 (pink). (C) IFS staining of endothelial marker CD31 (green) and contractile smooth muscle marker α-SMA (red). (D) IFS staining of contractile phenotypic smooth muscle cell marker α-SMA (red) and active proliferating cell marker Ki67 (green). W = wires; A = new vessel in neointima; the right column shows the magnified images of the yellow rectangular box in the corresponding left column of images.
    Figure Legend Snippet: Representative images of ( A ) H&E staining and ( B–D ) immunofluorescence (IFS) staining of vascular cross-sections of rat carotid arteries after 10 months of implantation. (B) IFS staining of macrophage marker CD68 (pink). (C) IFS staining of endothelial marker CD31 (green) and contractile smooth muscle marker α-SMA (red). (D) IFS staining of contractile phenotypic smooth muscle cell marker α-SMA (red) and active proliferating cell marker Ki67 (green). W = wires; A = new vessel in neointima; the right column shows the magnified images of the yellow rectangular box in the corresponding left column of images.

    Techniques Used: Staining, Immunofluorescence, Marker

    Related Articles

    Staining:

    Article Title: Zn ion-implanted absorbable Fe for improved cytocompatibility and mitigated neointimal hyperplasia
    Article Snippet: Human umbilical vein endothelial fusion cells (EA. hy926, ATCC CRL-2922, USA) were used to evaluate the impact of materials on cell adhesion and cytotoxicity.. Cells were cultured in Dulbecco’s Modified Eagle Medium (DMEM, Gibco, USA) containing 10% fetal bovine serum (FBS, Gibco, USA).Cells were cultured in Dulbecco’s Modified Eagle Medium (DMEM, Gibco, USA) containing 10% fetal bovine serum (FBS, Gibco, USA).

    Article Title: Zn ion-implanted absorbable Fe for improved cytocompatibility and mitigated neointimal hyperplasia
    Article Snippet: Human umbilical vein endothelial fusion cells (EA. hy926, ATCC CRL-2922, US) were used to evaluate the impact of materials on cell adhesion and cytotoxicity.. Cells were cultured in Dulbecco’s Modified Eagle Medium (DMEM, Gibco, US) containing 10% fetal bovine serum (FBS, Gibco, US).Cells were cultured in Dulbecco’s Modified Eagle Medium (DMEM, Gibco, US) containing 10% fetal bovine serum (FBS, Gibco, US).

    Immunofluorescence:

    Article Title: Zn ion-implanted absorbable Fe for improved cytocompatibility and mitigated neointimal hyperplasia
    Article Snippet: Human umbilical vein endothelial fusion cells (EA. hy926, ATCC CRL-2922, USA) were used to evaluate the impact of materials on cell adhesion and cytotoxicity.. Cells were cultured in Dulbecco’s Modified Eagle Medium (DMEM, Gibco, USA) containing 10% fetal bovine serum (FBS, Gibco, USA).Cells were cultured in Dulbecco’s Modified Eagle Medium (DMEM, Gibco, USA) containing 10% fetal bovine serum (FBS, Gibco, USA).

    Article Title: Zn ion-implanted absorbable Fe for improved cytocompatibility and mitigated neointimal hyperplasia
    Article Snippet: Human umbilical vein endothelial fusion cells (EA. hy926, ATCC CRL-2922, US) were used to evaluate the impact of materials on cell adhesion and cytotoxicity.. Cells were cultured in Dulbecco’s Modified Eagle Medium (DMEM, Gibco, US) containing 10% fetal bovine serum (FBS, Gibco, US).Cells were cultured in Dulbecco’s Modified Eagle Medium (DMEM, Gibco, US) containing 10% fetal bovine serum (FBS, Gibco, US).

    Marker:

    Article Title: Zn ion-implanted absorbable Fe for improved cytocompatibility and mitigated neointimal hyperplasia
    Article Snippet: Human umbilical vein endothelial fusion cells (EA. hy926, ATCC CRL-2922, USA) were used to evaluate the impact of materials on cell adhesion and cytotoxicity.. Cells were cultured in Dulbecco’s Modified Eagle Medium (DMEM, Gibco, USA) containing 10% fetal bovine serum (FBS, Gibco, USA).Cells were cultured in Dulbecco’s Modified Eagle Medium (DMEM, Gibco, USA) containing 10% fetal bovine serum (FBS, Gibco, USA).

    Article Title: Zn ion-implanted absorbable Fe for improved cytocompatibility and mitigated neointimal hyperplasia
    Article Snippet: Human umbilical vein endothelial fusion cells (EA. hy926, ATCC CRL-2922, US) were used to evaluate the impact of materials on cell adhesion and cytotoxicity.. Cells were cultured in Dulbecco’s Modified Eagle Medium (DMEM, Gibco, US) containing 10% fetal bovine serum (FBS, Gibco, US).Cells were cultured in Dulbecco’s Modified Eagle Medium (DMEM, Gibco, US) containing 10% fetal bovine serum (FBS, Gibco, US).



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    Representative images of ( A ) H&E staining and ( B–D ) immunofluorescence (IFS) staining of vascular cross-sections of rat carotid arteries after 10 months of implantation. (B) IFS staining of macrophage marker CD68 (pink). (C) IFS staining of <t>endothelial</t> marker CD31 (green) and contractile smooth muscle marker α-SMA (red). (D) IFS staining of contractile phenotypic smooth muscle cell marker α-SMA (red) and active proliferating cell marker Ki67 (green). W = wires; A = new vessel in neointima; the right column shows the magnified images of the yellow rectangular box in the corresponding left column of images.
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    Representative images of ( A ) H&E staining and ( B–D ) immunofluorescence (IFS) staining of vascular cross-sections of rat carotid arteries after 10 months of implantation. (B) IFS staining of macrophage marker CD68 (pink). (C) IFS staining of <t>endothelial</t> marker CD31 (green) and contractile smooth muscle marker α-SMA (red). (D) IFS staining of contractile phenotypic smooth muscle cell marker α-SMA (red) and active proliferating cell marker Ki67 (green). W = wires; A = new vessel in neointima; the right column shows the magnified images of the yellow rectangular box in the corresponding left column of images.
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    Representative images of ( A ) H&E staining and ( B–D ) immunofluorescence (IFS) staining of vascular cross-sections of rat carotid arteries after 10 months of implantation. (B) IFS staining of macrophage marker CD68 (pink). (C) IFS staining of <t>endothelial</t> marker CD31 (green) and contractile smooth muscle marker α-SMA (red). (D) IFS staining of contractile phenotypic smooth muscle cell marker α-SMA (red) and active proliferating cell marker Ki67 (green). W = wires; A = new vessel in neointima; the right column shows the magnified images of the yellow rectangular box in the corresponding left column of images.
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    Representative images of ( A ) H&E staining and ( B–D ) immunofluorescence (IFS) staining of vascular cross-sections of rat carotid arteries after 10 months of implantation. (B) IFS staining of macrophage marker CD68 (pink). (C) IFS staining of <t>endothelial</t> marker CD31 (green) and contractile smooth muscle marker α-SMA (red). (D) IFS staining of contractile phenotypic smooth muscle cell marker α-SMA (red) and active proliferating cell marker Ki67 (green). W = wires; A = new vessel in neointima; the right column shows the magnified images of the yellow rectangular box in the corresponding left column of images.
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    Image Search Results


    Representative images of ( A ) H&E staining and ( B–D ) immunofluorescence (IFS) staining of vascular cross-sections of rat carotid arteries after 10 months of implantation. (B) IFS staining of macrophage marker CD68 (pink). (C) IFS staining of endothelial marker CD31 (green) and contractile smooth muscle marker α-SMA (red). (D) IFS staining of contractile phenotypic smooth muscle cell marker α-SMA (red) and active proliferating cell marker Ki67 (green). W = wires; A = new vessel in neointima; the right column shows the magnified images of the yellow rectangular box in the corresponding left column of images.

    Journal: Regenerative Biomaterials

    Article Title: Zn ion-implanted absorbable Fe for improved cytocompatibility and mitigated neointimal hyperplasia

    doi: 10.1093/rb/rbaf112

    Figure Lengend Snippet: Representative images of ( A ) H&E staining and ( B–D ) immunofluorescence (IFS) staining of vascular cross-sections of rat carotid arteries after 10 months of implantation. (B) IFS staining of macrophage marker CD68 (pink). (C) IFS staining of endothelial marker CD31 (green) and contractile smooth muscle marker α-SMA (red). (D) IFS staining of contractile phenotypic smooth muscle cell marker α-SMA (red) and active proliferating cell marker Ki67 (green). W = wires; A = new vessel in neointima; the right column shows the magnified images of the yellow rectangular box in the corresponding left column of images.

    Article Snippet: Human umbilical vein endothelial fusion cells (EA. hy926, ATCC CRL-2922, USA) were used to evaluate the impact of materials on cell adhesion and cytotoxicity.

    Techniques: Staining, Immunofluorescence, Marker