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green fluorescent protein (gfp)-labeled huvecs  (Cellworks)

 
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    Structured Review

    Cellworks green fluorescent protein (gfp)-labeled huvecs
    Drug effect on vascular network formation. Vascular networks formed by co-culturing <t>green</t> <t>fluorescent</t> protein-labeled human umbilical vein endothelial cells <t>(GFP-HUVECs,</t> green) and BMSCs for 7 days in the presence of drugs or DMSO at the indicated concentrations. BMSCs are stained for pericytic marker α smooth muscle actin (α-SMA) shown in red. Scale bar: 200 µm.
    Green Fluorescent Protein (Gfp) Labeled Huvecs, supplied by Cellworks, 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/green fluorescent protein (gfp)-labeled huvecs/product/Cellworks
    Average 90 stars, based on 1 article reviews
    green fluorescent protein (gfp)-labeled huvecs - by Bioz Stars, 2026-02
    90/100 stars

    Images

    1) Product Images from "Growth Response and Differentiation of Bone Marrow-Derived Mesenchymal Stem/Stromal Cells in the Presence of Novel Multiple Myeloma Drug Melflufen"

    Article Title: Growth Response and Differentiation of Bone Marrow-Derived Mesenchymal Stem/Stromal Cells in the Presence of Novel Multiple Myeloma Drug Melflufen

    Journal: Cells

    doi: 10.3390/cells11091574

    Drug effect on vascular network formation. Vascular networks formed by co-culturing green fluorescent protein-labeled human umbilical vein endothelial cells (GFP-HUVECs, green) and BMSCs for 7 days in the presence of drugs or DMSO at the indicated concentrations. BMSCs are stained for pericytic marker α smooth muscle actin (α-SMA) shown in red. Scale bar: 200 µm.
    Figure Legend Snippet: Drug effect on vascular network formation. Vascular networks formed by co-culturing green fluorescent protein-labeled human umbilical vein endothelial cells (GFP-HUVECs, green) and BMSCs for 7 days in the presence of drugs or DMSO at the indicated concentrations. BMSCs are stained for pericytic marker α smooth muscle actin (α-SMA) shown in red. Scale bar: 200 µm.

    Techniques Used: Labeling, Staining, Marker

    Quantitative analysis of vascular network formation in the presence of drugs: ( a ) quantification of vascular area covered by GFP-HUVECs; ( b ) pericyte area covered by α smooth muscle actin (α-SMA)-positive BMSCs. Dots represent regions of interest from co-cultures involving color-coded donor BMSC lines with melflufen, melphalan, and doxorubicin added at indicated concentrations. Open circles indicate DMSO vehicle controls for 10 µM melphalan. * denotes p < 0.05, *** denotes p < 0.001 with Dunn’s test.
    Figure Legend Snippet: Quantitative analysis of vascular network formation in the presence of drugs: ( a ) quantification of vascular area covered by GFP-HUVECs; ( b ) pericyte area covered by α smooth muscle actin (α-SMA)-positive BMSCs. Dots represent regions of interest from co-cultures involving color-coded donor BMSC lines with melflufen, melphalan, and doxorubicin added at indicated concentrations. Open circles indicate DMSO vehicle controls for 10 µM melphalan. * denotes p < 0.05, *** denotes p < 0.001 with Dunn’s test.

    Techniques Used:



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    Image Search Results


    Drug effect on vascular network formation. Vascular networks formed by co-culturing green fluorescent protein-labeled human umbilical vein endothelial cells (GFP-HUVECs, green) and BMSCs for 7 days in the presence of drugs or DMSO at the indicated concentrations. BMSCs are stained for pericytic marker α smooth muscle actin (α-SMA) shown in red. Scale bar: 200 µm.

    Journal: Cells

    Article Title: Growth Response and Differentiation of Bone Marrow-Derived Mesenchymal Stem/Stromal Cells in the Presence of Novel Multiple Myeloma Drug Melflufen

    doi: 10.3390/cells11091574

    Figure Lengend Snippet: Drug effect on vascular network formation. Vascular networks formed by co-culturing green fluorescent protein-labeled human umbilical vein endothelial cells (GFP-HUVECs, green) and BMSCs for 7 days in the presence of drugs or DMSO at the indicated concentrations. BMSCs are stained for pericytic marker α smooth muscle actin (α-SMA) shown in red. Scale bar: 200 µm.

    Article Snippet: After 2 h, green fluorescent protein (GFP)-labeled HUVECs (CellWorks) were added at 4000 cells/cm 2 and cultured overnight in EGM-2.

    Techniques: Labeling, Staining, Marker

    Quantitative analysis of vascular network formation in the presence of drugs: ( a ) quantification of vascular area covered by GFP-HUVECs; ( b ) pericyte area covered by α smooth muscle actin (α-SMA)-positive BMSCs. Dots represent regions of interest from co-cultures involving color-coded donor BMSC lines with melflufen, melphalan, and doxorubicin added at indicated concentrations. Open circles indicate DMSO vehicle controls for 10 µM melphalan. * denotes p < 0.05, *** denotes p < 0.001 with Dunn’s test.

    Journal: Cells

    Article Title: Growth Response and Differentiation of Bone Marrow-Derived Mesenchymal Stem/Stromal Cells in the Presence of Novel Multiple Myeloma Drug Melflufen

    doi: 10.3390/cells11091574

    Figure Lengend Snippet: Quantitative analysis of vascular network formation in the presence of drugs: ( a ) quantification of vascular area covered by GFP-HUVECs; ( b ) pericyte area covered by α smooth muscle actin (α-SMA)-positive BMSCs. Dots represent regions of interest from co-cultures involving color-coded donor BMSC lines with melflufen, melphalan, and doxorubicin added at indicated concentrations. Open circles indicate DMSO vehicle controls for 10 µM melphalan. * denotes p < 0.05, *** denotes p < 0.001 with Dunn’s test.

    Article Snippet: After 2 h, green fluorescent protein (GFP)-labeled HUVECs (CellWorks) were added at 4000 cells/cm 2 and cultured overnight in EGM-2.

    Techniques: