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endothelial growth media  (Cell Applications Inc)


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    Cell Applications Inc endothelial growth media
    Endothelial Growth Media, supplied by Cell Applications Inc, used in various techniques. Bioz Stars score: 95/100, based on 96 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/endothelial+cell+growth+media/Human+Endothelial+Cell+Media/bio_rxiv__64898__2026__05__04__722602-33-41-47
    Average 95 stars, based on 96 article reviews
    endothelial growth media - by Bioz Stars, 2026-10
    95/100 stars

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    Cell Culture:

    Article Title: Hutchinson-Gilford progeria syndrome alters the endothelial genetic response to laminar shear stress
    Article Snippet: .. HUVECs were provided by Clonetics and were cultured on T-75 flasks in 15 mL Endothelial Cell Growth Media (Cell Applications). ..

    Article Title: Single-Cell Metabolic Imaging Reveals Glycogen-Driven Adaptations in Endothelial Cells.
    Article Snippet: .. HUVECs (passages 5-8; Cell Applications, Cat. #200-05n) were tested negative for mycoplasma contamination and cultured at 37 °C with 5% CO2 in commercial endothelial cell growth media (ECGM; Cell Applications, Cat. #211-500), supplemented with 10% FBS (Corning, Cat. #35-015-CV) and 100x antibioticantimycotic (Gibco, Cat. #15240062). .. HeLa cells (ATCC, CCL-2) were cultured in DMEM (Corning, Cat. #10-017-CV) with the same supplementation as above.

    Article Title: Single‐Cell Metabolic Imaging Reveals Glycogen‐Driven Adaptations in Endothelial Cells
    Article Snippet: .. HUVECs (passages 5‐8; Cell Applications, Cat. #200‐05n) were tested negative for mycoplasma contamination and cultured at 37 °C with 5% CO 2 in commercial endothelial cell growth media (ECGM; Cell Applications, Cat. #211‐500), supplemented with 10% FBS (Corning, Cat. #35‐015‐CV) and 100x antibiotic‐antimycotic (Gibco, Cat. #15240062). .. HeLa cells (ATCC, CCL‐2) were cultured in DMEM (Corning, Cat. #10‐017‐CV) with the same supplementation as above.

    Article Title: Single-Cell Metabolic Imaging Reveals Glycogen Driven-Adaptations in Endothelial Cells
    Article Snippet: .. HUVECs (passages 5-8; Cell Applications, Cat. #200-05n) were tested negative for mycoplasma contamination and cultured at 37°C with 5% CO 2 in commercial endothelial cell growth media (ECGM; Cell Applications, Cat. #211-500), supplemented with 10% FBS (Corning, Cat. #35-015-CV) and 100× antibiotic-antimycotic (Gibco, Cat. #15240062). .. HeLa cells (ATCC, CCL-2) were cultured in DMEM (Corning, Cat. #10-017-CV) with the same supplementation as above.



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    Effect of extrusion process on μRB bioink and cell alignment. (A) Schematic of MSCs encapsulated in μRB bioink with HUVECs seeded on top of the printed scaffolds. (B) Live cell staining of MSC alignment on individual μRBs (Scale bar = 100 μm). (C) Distribution of MSC cell length (n = 250 per group); p-values were determined by one-way analysis of variance (ANOVA) with Tukey's multiple comparisons test; ∗∗∗∗p < 0.0001. (D) Cell orientation relative to μRB orientation, where 0° is parallel to the axis of the μRB (n = 250 per group). (E) Confocal images of F-Actin staining for cell morphology and VE-cadherin staining for <t>endothelial</t> cell junctions. Color survey visualization of directional analysis conducted using OrientationJ (Scale bar = 200 μm). (F, G) Quantification of F-actin and VE-Cadherin alignment. For alignment quantification (n = 10 per group) data reported as mean ± S.D., statistical analysis by Watson–Wheeler test, ∗p ≤ 0.05.
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    Effect of extrusion process on μRB bioink and cell alignment. (A) Schematic of MSCs encapsulated in μRB bioink with HUVECs seeded on top of the printed scaffolds. (B) Live cell staining of MSC alignment on individual μRBs (Scale bar = 100 μm). (C) Distribution of MSC cell length (n = 250 per group); p-values were determined by one-way analysis of variance (ANOVA) with Tukey's multiple comparisons test; ∗∗∗∗p < 0.0001. (D) Cell orientation relative to μRB orientation, where 0° is parallel to the axis of the μRB (n = 250 per group). (E) Confocal images of F-Actin staining for cell morphology and VE-cadherin staining for <t>endothelial</t> cell junctions. Color survey visualization of directional analysis conducted using OrientationJ (Scale bar = 200 μm). (F, G) Quantification of F-actin and VE-Cadherin alignment. For alignment quantification (n = 10 per group) data reported as mean ± S.D., statistical analysis by Watson–Wheeler test, ∗p ≤ 0.05.
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    Image Search Results


    Effect of extrusion process on μRB bioink and cell alignment. (A) Schematic of MSCs encapsulated in μRB bioink with HUVECs seeded on top of the printed scaffolds. (B) Live cell staining of MSC alignment on individual μRBs (Scale bar = 100 μm). (C) Distribution of MSC cell length (n = 250 per group); p-values were determined by one-way analysis of variance (ANOVA) with Tukey's multiple comparisons test; ∗∗∗∗p < 0.0001. (D) Cell orientation relative to μRB orientation, where 0° is parallel to the axis of the μRB (n = 250 per group). (E) Confocal images of F-Actin staining for cell morphology and VE-cadherin staining for endothelial cell junctions. Color survey visualization of directional analysis conducted using OrientationJ (Scale bar = 200 μm). (F, G) Quantification of F-actin and VE-Cadherin alignment. For alignment quantification (n = 10 per group) data reported as mean ± S.D., statistical analysis by Watson–Wheeler test, ∗p ≤ 0.05.

    Journal: Bioactive Materials

    Article Title: Ribbon-shaped microgels as bioinks for 3D bioprinting of anisotropic tissue structures

    doi: 10.1016/j.bioactmat.2025.12.040

    Figure Lengend Snippet: Effect of extrusion process on μRB bioink and cell alignment. (A) Schematic of MSCs encapsulated in μRB bioink with HUVECs seeded on top of the printed scaffolds. (B) Live cell staining of MSC alignment on individual μRBs (Scale bar = 100 μm). (C) Distribution of MSC cell length (n = 250 per group); p-values were determined by one-way analysis of variance (ANOVA) with Tukey's multiple comparisons test; ∗∗∗∗p < 0.0001. (D) Cell orientation relative to μRB orientation, where 0° is parallel to the axis of the μRB (n = 250 per group). (E) Confocal images of F-Actin staining for cell morphology and VE-cadherin staining for endothelial cell junctions. Color survey visualization of directional analysis conducted using OrientationJ (Scale bar = 200 μm). (F, G) Quantification of F-actin and VE-Cadherin alignment. For alignment quantification (n = 10 per group) data reported as mean ± S.D., statistical analysis by Watson–Wheeler test, ∗p ≤ 0.05.

    Article Snippet: Human umbilical vein endothelial cells (HUVECs, Lonza) were cultured in Endothelial Cell Growth Media (R&D Systems).

    Techniques: Staining