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Procell Inc rat umbilical vein endothelial cells (uvecs)
Toxic effects of GOG@WK-EVs on cells. (a) Co-cultured materials with various groups of cells for 6, 12, 24, and 48 h and evaluated the cell status and viability of BMSCs, <t>UVECs,</t> and BMMs using live/dead cell staining and MTT assay; (b) Assessed cell survival and proliferation of BMSCs, UVECs, and BMMs using CCK-8 assay; (c) Examined the cytoskeletal structure of BMSCs, UVECs, and BMMs through immunofluorescence staining, where phalloidin staining indicated cytoskeleton in green, DAPI staining showed nuclei in blue, scale bar: 50 μm. * denotes statistical significance at p < 0.05 between two groups and the cell experiments were repeated three times.
Rat Umbilical Vein Endothelial Cells (Uvecs), supplied by Procell Inc, 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/rat+umbilical+vein+endothelial+cells+%28uvecs%29/pmc11662390-28-0-9?v=Procell+Inc
Average 90 stars, based on 1 article reviews
rat umbilical vein endothelial cells (uvecs) - by Bioz Stars, 2026-06
90/100 stars

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1) Product Images from "Harnessing bone marrow mesenchymal stem cell-derived extracellular vesicles and biomimetic peptide WKYMVm in self-healing hydrogel for enhanced bone repair in femoral defects"

Article Title: Harnessing bone marrow mesenchymal stem cell-derived extracellular vesicles and biomimetic peptide WKYMVm in self-healing hydrogel for enhanced bone repair in femoral defects

Journal: Journal of Tissue Engineering

doi: 10.1177/20417314241306681

Toxic effects of GOG@WK-EVs on cells. (a) Co-cultured materials with various groups of cells for 6, 12, 24, and 48 h and evaluated the cell status and viability of BMSCs, UVECs, and BMMs using live/dead cell staining and MTT assay; (b) Assessed cell survival and proliferation of BMSCs, UVECs, and BMMs using CCK-8 assay; (c) Examined the cytoskeletal structure of BMSCs, UVECs, and BMMs through immunofluorescence staining, where phalloidin staining indicated cytoskeleton in green, DAPI staining showed nuclei in blue, scale bar: 50 μm. * denotes statistical significance at p < 0.05 between two groups and the cell experiments were repeated three times.
Figure Legend Snippet: Toxic effects of GOG@WK-EVs on cells. (a) Co-cultured materials with various groups of cells for 6, 12, 24, and 48 h and evaluated the cell status and viability of BMSCs, UVECs, and BMMs using live/dead cell staining and MTT assay; (b) Assessed cell survival and proliferation of BMSCs, UVECs, and BMMs using CCK-8 assay; (c) Examined the cytoskeletal structure of BMSCs, UVECs, and BMMs through immunofluorescence staining, where phalloidin staining indicated cytoskeleton in green, DAPI staining showed nuclei in blue, scale bar: 50 μm. * denotes statistical significance at p < 0.05 between two groups and the cell experiments were repeated three times.

Techniques Used: Cell Culture, Staining, MTT Assay, CCK-8 Assay, Immunofluorescence

Impact of GOG@WK-EVs on vascular formation in UVECs. (a) Transwell assay to evaluate the migration of UVECs in each group, scale bar: 50 μm; (b) Scratch assay to measure the migration distance of UVECs in each group, scale bar: 100 μm; (c) Observation of the vascular formation capacity of UVECs in each group under an optical microscope, scale bar: 100 μm; (d) Number of branch points formed by UVECs in each group as depicted in Figure C; (E) Total length of tubes formed by UVECs in each group as depicted in Figure c; (f) Gene expression levels of key vascular formation factors (Ang, Pecam1, and Vcam1) in UVECs in each group assessed by RT-qPCR. * indicates a statistically significant difference ( p < 0.05) between the two groups, with cell experiments repeated three times.
Figure Legend Snippet: Impact of GOG@WK-EVs on vascular formation in UVECs. (a) Transwell assay to evaluate the migration of UVECs in each group, scale bar: 50 μm; (b) Scratch assay to measure the migration distance of UVECs in each group, scale bar: 100 μm; (c) Observation of the vascular formation capacity of UVECs in each group under an optical microscope, scale bar: 100 μm; (d) Number of branch points formed by UVECs in each group as depicted in Figure C; (E) Total length of tubes formed by UVECs in each group as depicted in Figure c; (f) Gene expression levels of key vascular formation factors (Ang, Pecam1, and Vcam1) in UVECs in each group assessed by RT-qPCR. * indicates a statistically significant difference ( p < 0.05) between the two groups, with cell experiments repeated three times.

Techniques Used: Transwell Assay, Migration, Wound Healing Assay, Microscopy, Gene Expression, Quantitative RT-PCR



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Procell Inc rat umbilical vein endothelial cells (uvecs)
Toxic effects of GOG@WK-EVs on cells. (a) Co-cultured materials with various groups of cells for 6, 12, 24, and 48 h and evaluated the cell status and viability of BMSCs, <t>UVECs,</t> and BMMs using live/dead cell staining and MTT assay; (b) Assessed cell survival and proliferation of BMSCs, UVECs, and BMMs using CCK-8 assay; (c) Examined the cytoskeletal structure of BMSCs, UVECs, and BMMs through immunofluorescence staining, where phalloidin staining indicated cytoskeleton in green, DAPI staining showed nuclei in blue, scale bar: 50 μm. * denotes statistical significance at p < 0.05 between two groups and the cell experiments were repeated three times.
Rat Umbilical Vein Endothelial Cells (Uvecs), supplied by Procell Inc, 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/rat+umbilical+vein+endothelial+cells+%28uvecs%29/pmc11662390-28-0-9?v=Procell+Inc
Average 90 stars, based on 1 article reviews
rat umbilical vein endothelial cells (uvecs) - by Bioz Stars, 2026-06
90/100 stars
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Toxic effects of GOG@WK-EVs on cells. (a) Co-cultured materials with various groups of cells for 6, 12, 24, and 48 h and evaluated the cell status and viability of BMSCs, UVECs, and BMMs using live/dead cell staining and MTT assay; (b) Assessed cell survival and proliferation of BMSCs, UVECs, and BMMs using CCK-8 assay; (c) Examined the cytoskeletal structure of BMSCs, UVECs, and BMMs through immunofluorescence staining, where phalloidin staining indicated cytoskeleton in green, DAPI staining showed nuclei in blue, scale bar: 50 μm. * denotes statistical significance at p < 0.05 between two groups and the cell experiments were repeated three times.

Journal: Journal of Tissue Engineering

Article Title: Harnessing bone marrow mesenchymal stem cell-derived extracellular vesicles and biomimetic peptide WKYMVm in self-healing hydrogel for enhanced bone repair in femoral defects

doi: 10.1177/20417314241306681

Figure Lengend Snippet: Toxic effects of GOG@WK-EVs on cells. (a) Co-cultured materials with various groups of cells for 6, 12, 24, and 48 h and evaluated the cell status and viability of BMSCs, UVECs, and BMMs using live/dead cell staining and MTT assay; (b) Assessed cell survival and proliferation of BMSCs, UVECs, and BMMs using CCK-8 assay; (c) Examined the cytoskeletal structure of BMSCs, UVECs, and BMMs through immunofluorescence staining, where phalloidin staining indicated cytoskeleton in green, DAPI staining showed nuclei in blue, scale bar: 50 μm. * denotes statistical significance at p < 0.05 between two groups and the cell experiments were repeated three times.

Article Snippet: Rat umbilical vein endothelial cells (UVECs) were obtained from Procell (Catalog Number: CP-R232) and cultured in endothelial cell medium (ECM, Catalog Number: 1001, Wegene, China) supplemented with 5% fetal bovine serum, 1% v/v penicillin/streptomycin, and 1% ECGS (Catalog Number: KGY1052, KGI, China) at 37°C in a 5% CO 2 environment.

Techniques: Cell Culture, Staining, MTT Assay, CCK-8 Assay, Immunofluorescence

Impact of GOG@WK-EVs on vascular formation in UVECs. (a) Transwell assay to evaluate the migration of UVECs in each group, scale bar: 50 μm; (b) Scratch assay to measure the migration distance of UVECs in each group, scale bar: 100 μm; (c) Observation of the vascular formation capacity of UVECs in each group under an optical microscope, scale bar: 100 μm; (d) Number of branch points formed by UVECs in each group as depicted in Figure C; (E) Total length of tubes formed by UVECs in each group as depicted in Figure c; (f) Gene expression levels of key vascular formation factors (Ang, Pecam1, and Vcam1) in UVECs in each group assessed by RT-qPCR. * indicates a statistically significant difference ( p < 0.05) between the two groups, with cell experiments repeated three times.

Journal: Journal of Tissue Engineering

Article Title: Harnessing bone marrow mesenchymal stem cell-derived extracellular vesicles and biomimetic peptide WKYMVm in self-healing hydrogel for enhanced bone repair in femoral defects

doi: 10.1177/20417314241306681

Figure Lengend Snippet: Impact of GOG@WK-EVs on vascular formation in UVECs. (a) Transwell assay to evaluate the migration of UVECs in each group, scale bar: 50 μm; (b) Scratch assay to measure the migration distance of UVECs in each group, scale bar: 100 μm; (c) Observation of the vascular formation capacity of UVECs in each group under an optical microscope, scale bar: 100 μm; (d) Number of branch points formed by UVECs in each group as depicted in Figure C; (E) Total length of tubes formed by UVECs in each group as depicted in Figure c; (f) Gene expression levels of key vascular formation factors (Ang, Pecam1, and Vcam1) in UVECs in each group assessed by RT-qPCR. * indicates a statistically significant difference ( p < 0.05) between the two groups, with cell experiments repeated three times.

Article Snippet: Rat umbilical vein endothelial cells (UVECs) were obtained from Procell (Catalog Number: CP-R232) and cultured in endothelial cell medium (ECM, Catalog Number: 1001, Wegene, China) supplemented with 5% fetal bovine serum, 1% v/v penicillin/streptomycin, and 1% ECGS (Catalog Number: KGY1052, KGI, China) at 37°C in a 5% CO 2 environment.

Techniques: Transwell Assay, Migration, Wound Healing Assay, Microscopy, Gene Expression, Quantitative RT-PCR