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cell culture human umbilical vein endothelial cells huvecs  (ATCC)


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    ATCC cell culture human umbilical vein endothelial cells huvecs
    Cell Culture Human Umbilical Vein Endothelial Cells Huvecs, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 4841 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 99 stars, based on 4841 article reviews
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    Effect of coating agents on the attachment and growth of <t>Endothelial</t> cells (ECs) on precision cut lung slices (PCLS). ( A ) Schematic diagram describes the experimental design of each assay using decellularized PCLS. ( B , C ) Coating of decellularized scaffolds enhance the attachment of Hoechst 33,342-labeled (blue) mC166 cells on PCLS compared to the uncoated group. Each group n = 6. ( D ) Quantification of EC cell metabolic activity using cell growth assay using Cell Counting Kit-8 (CCK-8) revealed that precoating of PCLS increases ECs growth and metabolic activity (Optical Density (OD) measured at Day 1, 3 and 5) compared to ECs cultured on uncoated PCLS. Each group n = 6. ( E ) Quantification of the attachment of Hoechst-labeled HUVECs on anti-CD31 coated PCLS coated with 12.5, 25, 50, or 100 µg/mL anti-CD31 Ab. Results represent the mean of measurements taken from 3 PCLS seeded with <t>HUVEC</t> cells from 3 independent experiments. Each group n = 3. ( F ) Quantification of HUVEC cell metabolic activity using cell growth assay using Cell Counting Kit-8 (CCK-8) revealed that precoating of PCLS increases ECs growth and metabolic activity (Optical Density (OD) measured at Day 1, 3 and 5) compared to ECs cultured on uncoated PCLS. Each group n = 3. Scale bar = 200 μm. The results represent the mean of measurements taken from 3 technical replicates. Each number represents a biological replicate (independent experiment). M ean ± SD, * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001
    Culture Human Umbilical Vein Endothelial Cells Huvec, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC culture human umbilical vein 206 endothelial cells huvec
    Effect of coating agents on the attachment and growth of <t>Endothelial</t> cells (ECs) on precision cut lung slices (PCLS). ( A ) Schematic diagram describes the experimental design of each assay using decellularized PCLS. ( B , C ) Coating of decellularized scaffolds enhance the attachment of Hoechst 33,342-labeled (blue) mC166 cells on PCLS compared to the uncoated group. Each group n = 6. ( D ) Quantification of EC cell metabolic activity using cell growth assay using Cell Counting Kit-8 (CCK-8) revealed that precoating of PCLS increases ECs growth and metabolic activity (Optical Density (OD) measured at Day 1, 3 and 5) compared to ECs cultured on uncoated PCLS. Each group n = 6. ( E ) Quantification of the attachment of Hoechst-labeled HUVECs on anti-CD31 coated PCLS coated with 12.5, 25, 50, or 100 µg/mL anti-CD31 Ab. Results represent the mean of measurements taken from 3 PCLS seeded with <t>HUVEC</t> cells from 3 independent experiments. Each group n = 3. ( F ) Quantification of HUVEC cell metabolic activity using cell growth assay using Cell Counting Kit-8 (CCK-8) revealed that precoating of PCLS increases ECs growth and metabolic activity (Optical Density (OD) measured at Day 1, 3 and 5) compared to ECs cultured on uncoated PCLS. Each group n = 3. Scale bar = 200 μm. The results represent the mean of measurements taken from 3 technical replicates. Each number represents a biological replicate (independent experiment). M ean ± SD, * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001
    Culture Human Umbilical Vein 206 Endothelial Cells Huvec, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC human umbilical vein endothelial cells huvecs american type culture collection
    Effect of coating agents on the attachment and growth of <t>Endothelial</t> cells (ECs) on precision cut lung slices (PCLS). ( A ) Schematic diagram describes the experimental design of each assay using decellularized PCLS. ( B , C ) Coating of decellularized scaffolds enhance the attachment of Hoechst 33,342-labeled (blue) mC166 cells on PCLS compared to the uncoated group. Each group n = 6. ( D ) Quantification of EC cell metabolic activity using cell growth assay using Cell Counting Kit-8 (CCK-8) revealed that precoating of PCLS increases ECs growth and metabolic activity (Optical Density (OD) measured at Day 1, 3 and 5) compared to ECs cultured on uncoated PCLS. Each group n = 6. ( E ) Quantification of the attachment of Hoechst-labeled HUVECs on anti-CD31 coated PCLS coated with 12.5, 25, 50, or 100 µg/mL anti-CD31 Ab. Results represent the mean of measurements taken from 3 PCLS seeded with <t>HUVEC</t> cells from 3 independent experiments. Each group n = 3. ( F ) Quantification of HUVEC cell metabolic activity using cell growth assay using Cell Counting Kit-8 (CCK-8) revealed that precoating of PCLS increases ECs growth and metabolic activity (Optical Density (OD) measured at Day 1, 3 and 5) compared to ECs cultured on uncoated PCLS. Each group n = 3. Scale bar = 200 μm. The results represent the mean of measurements taken from 3 technical replicates. Each number represents a biological replicate (independent experiment). M ean ± SD, * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001
    Human Umbilical Vein Endothelial Cells Huvecs American Type Culture Collection, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Effect of coating agents on the attachment and growth of <t>Endothelial</t> cells (ECs) on precision cut lung slices (PCLS). ( A ) Schematic diagram describes the experimental design of each assay using decellularized PCLS. ( B , C ) Coating of decellularized scaffolds enhance the attachment of Hoechst 33,342-labeled (blue) mC166 cells on PCLS compared to the uncoated group. Each group n = 6. ( D ) Quantification of EC cell metabolic activity using cell growth assay using Cell Counting Kit-8 (CCK-8) revealed that precoating of PCLS increases ECs growth and metabolic activity (Optical Density (OD) measured at Day 1, 3 and 5) compared to ECs cultured on uncoated PCLS. Each group n = 6. ( E ) Quantification of the attachment of Hoechst-labeled HUVECs on anti-CD31 coated PCLS coated with 12.5, 25, 50, or 100 µg/mL anti-CD31 Ab. Results represent the mean of measurements taken from 3 PCLS seeded with <t>HUVEC</t> cells from 3 independent experiments. Each group n = 3. ( F ) Quantification of HUVEC cell metabolic activity using cell growth assay using Cell Counting Kit-8 (CCK-8) revealed that precoating of PCLS increases ECs growth and metabolic activity (Optical Density (OD) measured at Day 1, 3 and 5) compared to ECs cultured on uncoated PCLS. Each group n = 3. Scale bar = 200 μm. The results represent the mean of measurements taken from 3 technical replicates. Each number represents a biological replicate (independent experiment). M ean ± SD, * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001
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    Angiogenesis effect of the self-assembled hybrid microspheres-based BM-mimicking niche. A-E) Results from the groups without BMSCs: A, B) Representative Transwell migration images and the quantitative assessment of <t>HUVECs</t> numbers based on the crystal violet staining results on day 1. C, D) Representative scratch assay images and the quantitative analysis of migration rate of HUVECs on day 1. E-F) Representative images and quantitative assessment of tube-like structure formation of HUVECs induced by released peptides at 6 h. G-H) Representative images and quantitative assessment of tube-like structure formation of <t>HUVECs</t> <t>cultured</t> in the conditioned medium from surface-adhesive BMSCs at 6 h. I) Expression of angiogenesis-related genes of HUVECs cultured in the conditioned medium from surface-adhesive BMSCs (VEGF, PDGF, FGF, CD31, α-SMA, and eNOS) on day 3. J-K) Representative images and quantitative assessment of tube-like structure formation of HUVECs cultured in the conditioned medium from encapsulated BMSCs at 6 h. L) Angiogenesis-related gene expression of HUVECs cultured in the conditioned medium from encapsulated BMSC on day 3. (ns = no significant difference, ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, n = 3).
    Huvecs Complete Culture Medium, supplied by Procell Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Procell Inc cell culture human umbilical vein endothelial cells huvecs
    Angiogenesis effect of the self-assembled hybrid microspheres-based BM-mimicking niche. A-E) Results from the groups without BMSCs: A, B) Representative Transwell migration images and the quantitative assessment of <t>HUVECs</t> numbers based on the crystal violet staining results on day 1. C, D) Representative scratch assay images and the quantitative analysis of migration rate of HUVECs on day 1. E-F) Representative images and quantitative assessment of tube-like structure formation of HUVECs induced by released peptides at 6 h. G-H) Representative images and quantitative assessment of tube-like structure formation of <t>HUVECs</t> <t>cultured</t> in the conditioned medium from surface-adhesive BMSCs at 6 h. I) Expression of angiogenesis-related genes of HUVECs cultured in the conditioned medium from surface-adhesive BMSCs (VEGF, PDGF, FGF, CD31, α-SMA, and eNOS) on day 3. J-K) Representative images and quantitative assessment of tube-like structure formation of HUVECs cultured in the conditioned medium from encapsulated BMSCs at 6 h. L) Angiogenesis-related gene expression of HUVECs cultured in the conditioned medium from encapsulated BMSC on day 3. (ns = no significant difference, ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, n = 3).
    Cell Culture Human Umbilical Vein Endothelial Cells Huvecs, supplied by Procell Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Effect of coating agents on the attachment and growth of Endothelial cells (ECs) on precision cut lung slices (PCLS). ( A ) Schematic diagram describes the experimental design of each assay using decellularized PCLS. ( B , C ) Coating of decellularized scaffolds enhance the attachment of Hoechst 33,342-labeled (blue) mC166 cells on PCLS compared to the uncoated group. Each group n = 6. ( D ) Quantification of EC cell metabolic activity using cell growth assay using Cell Counting Kit-8 (CCK-8) revealed that precoating of PCLS increases ECs growth and metabolic activity (Optical Density (OD) measured at Day 1, 3 and 5) compared to ECs cultured on uncoated PCLS. Each group n = 6. ( E ) Quantification of the attachment of Hoechst-labeled HUVECs on anti-CD31 coated PCLS coated with 12.5, 25, 50, or 100 µg/mL anti-CD31 Ab. Results represent the mean of measurements taken from 3 PCLS seeded with HUVEC cells from 3 independent experiments. Each group n = 3. ( F ) Quantification of HUVEC cell metabolic activity using cell growth assay using Cell Counting Kit-8 (CCK-8) revealed that precoating of PCLS increases ECs growth and metabolic activity (Optical Density (OD) measured at Day 1, 3 and 5) compared to ECs cultured on uncoated PCLS. Each group n = 3. Scale bar = 200 μm. The results represent the mean of measurements taken from 3 technical replicates. Each number represents a biological replicate (independent experiment). M ean ± SD, * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001

    Journal: Journal of Biological Engineering

    Article Title: Anti-CD31 antibody preconditioning for enhancement of endothelial cell capture and vascularization: a novel strategy for bioengineering lung scaffolds

    doi: 10.1186/s13036-025-00593-x

    Figure Lengend Snippet: Effect of coating agents on the attachment and growth of Endothelial cells (ECs) on precision cut lung slices (PCLS). ( A ) Schematic diagram describes the experimental design of each assay using decellularized PCLS. ( B , C ) Coating of decellularized scaffolds enhance the attachment of Hoechst 33,342-labeled (blue) mC166 cells on PCLS compared to the uncoated group. Each group n = 6. ( D ) Quantification of EC cell metabolic activity using cell growth assay using Cell Counting Kit-8 (CCK-8) revealed that precoating of PCLS increases ECs growth and metabolic activity (Optical Density (OD) measured at Day 1, 3 and 5) compared to ECs cultured on uncoated PCLS. Each group n = 6. ( E ) Quantification of the attachment of Hoechst-labeled HUVECs on anti-CD31 coated PCLS coated with 12.5, 25, 50, or 100 µg/mL anti-CD31 Ab. Results represent the mean of measurements taken from 3 PCLS seeded with HUVEC cells from 3 independent experiments. Each group n = 3. ( F ) Quantification of HUVEC cell metabolic activity using cell growth assay using Cell Counting Kit-8 (CCK-8) revealed that precoating of PCLS increases ECs growth and metabolic activity (Optical Density (OD) measured at Day 1, 3 and 5) compared to ECs cultured on uncoated PCLS. Each group n = 3. Scale bar = 200 μm. The results represent the mean of measurements taken from 3 technical replicates. Each number represents a biological replicate (independent experiment). M ean ± SD, * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001

    Article Snippet: Endothelial cell growth medium (EGM) (Lonza Bioscience, MD, USA) was used to culture human umbilical vein endothelial cells (HUVEC) (ATCC, Manassas, VA).

    Techniques: Labeling, Activity Assay, Growth Assay, Cell Counting, CCK-8 Assay, Cell Culture

    Angiogenesis effect of the self-assembled hybrid microspheres-based BM-mimicking niche. A-E) Results from the groups without BMSCs: A, B) Representative Transwell migration images and the quantitative assessment of HUVECs numbers based on the crystal violet staining results on day 1. C, D) Representative scratch assay images and the quantitative analysis of migration rate of HUVECs on day 1. E-F) Representative images and quantitative assessment of tube-like structure formation of HUVECs induced by released peptides at 6 h. G-H) Representative images and quantitative assessment of tube-like structure formation of HUVECs cultured in the conditioned medium from surface-adhesive BMSCs at 6 h. I) Expression of angiogenesis-related genes of HUVECs cultured in the conditioned medium from surface-adhesive BMSCs (VEGF, PDGF, FGF, CD31, α-SMA, and eNOS) on day 3. J-K) Representative images and quantitative assessment of tube-like structure formation of HUVECs cultured in the conditioned medium from encapsulated BMSCs at 6 h. L) Angiogenesis-related gene expression of HUVECs cultured in the conditioned medium from encapsulated BMSC on day 3. (ns = no significant difference, ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, n = 3).

    Journal: Bioactive Materials

    Article Title: Self-assembled hybrid hydrogel microspheres create a bone marrow-mimicking niche for bone regeneration

    doi: 10.1016/j.bioactmat.2025.08.003

    Figure Lengend Snippet: Angiogenesis effect of the self-assembled hybrid microspheres-based BM-mimicking niche. A-E) Results from the groups without BMSCs: A, B) Representative Transwell migration images and the quantitative assessment of HUVECs numbers based on the crystal violet staining results on day 1. C, D) Representative scratch assay images and the quantitative analysis of migration rate of HUVECs on day 1. E-F) Representative images and quantitative assessment of tube-like structure formation of HUVECs induced by released peptides at 6 h. G-H) Representative images and quantitative assessment of tube-like structure formation of HUVECs cultured in the conditioned medium from surface-adhesive BMSCs at 6 h. I) Expression of angiogenesis-related genes of HUVECs cultured in the conditioned medium from surface-adhesive BMSCs (VEGF, PDGF, FGF, CD31, α-SMA, and eNOS) on day 3. J-K) Representative images and quantitative assessment of tube-like structure formation of HUVECs cultured in the conditioned medium from encapsulated BMSCs at 6 h. L) Angiogenesis-related gene expression of HUVECs cultured in the conditioned medium from encapsulated BMSC on day 3. (ns = no significant difference, ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, n = 3).

    Article Snippet: Human umbilical vein endothelial cells (HUVECs, Procell, China) were cultured in the HUVECs complete culture medium (Procell, China) at 37 °C with 5 % CO 2 .

    Techniques: Migration, Staining, Wound Healing Assay, Cell Culture, Adhesive, Expressing, Gene Expression