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dermal neonatal human lymphatic microvascular endothelial cells, lecs cc-2812  (Cambrex)

 
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    Cambrex dermal neonatal human lymphatic microvascular endothelial cells, lecs cc-2812
    Dermal Neonatal Human Lymphatic Microvascular Endothelial Cells, Lecs Cc 2812, supplied by Cambrex, 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/neonatal+human+dermal+lecs/neonatal+human+dermal+lymphatic+microvascular+endothelial+cells++lecs+/pmc03287291-63-10-13
    Average 90 stars, based on 1 article reviews
    dermal neonatal human lymphatic microvascular endothelial cells, lecs cc-2812 - by Bioz Stars, 2026-10
    90/100 stars

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    other:

    Article Title: Endothelial Nitric Oxide Synthase Mediates Lymphangiogenesis and Lymphatic Metastasis
    Article Snippet: Neonatal Human Dermal LECs were obtained from Cambrex.



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    A , Prostatic LEC tube length at 4.5 hours post VEGF-C treatment was quantified using ImageJ. VEGF-C significantly increased the number of tubes formed compared to vehicle control. Data expressed as mean±s.e.m., n = 3, *** P <0.001 using One-way ANOVA, Bonferroni post-analysis. B , Western blotting analysis of VEGFR-2 and VEGFR-3 expression in <t>lung,</t> <t>neonatal</t> dermis and prostate <t>LECs.</t> β-tubulin was used as a loading control.
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    Lonza neonatal human dermal lymphatic microvascular endothelial cells (lec)
    A , Prostatic LEC tube length at 4.5 hours post VEGF-C treatment was quantified using ImageJ. VEGF-C significantly increased the number of tubes formed compared to vehicle control. Data expressed as mean±s.e.m., n = 3, *** P <0.001 using One-way ANOVA, Bonferroni post-analysis. B , Western blotting analysis of VEGFR-2 and VEGFR-3 expression in <t>lung,</t> <t>neonatal</t> dermis and prostate <t>LECs.</t> β-tubulin was used as a loading control.
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    Image Search Results


    Suppression of vascular endothelial growth factor (VEGF)‐C‐driven lymphatic endothelial cell (LEC) proliferation by conditioned medium of soluble vascular endothelial growth factor receptor‐3 (sVEGFR‐3)‐expressing cells. Cells were plated at 5 × 103 cells/well in 96‐well plates, and 50% sVEGFR‐3‐conditioned medium or luciferase‐conditioned medium was added with 100 ng/mL recombinant human VEGF‐C. The number of LEC with 50% sVEGFR‐3‐conditioned medium (b) was clearly smaller than that with control (a). The cells were counted by colorimetric assay 48 h after plating. Each bar represents the mean ± SD. (*P < 0.01) (c).

    Journal: Cancer Science

    Article Title: Suppression of lymph node and lung metastases of endometrial cancer by muscle‐mediated expression of soluble vascular endothelial growth factor receptor‐3

    doi: 10.1111/cas.12184

    Figure Lengend Snippet: Suppression of vascular endothelial growth factor (VEGF)‐C‐driven lymphatic endothelial cell (LEC) proliferation by conditioned medium of soluble vascular endothelial growth factor receptor‐3 (sVEGFR‐3)‐expressing cells. Cells were plated at 5 × 103 cells/well in 96‐well plates, and 50% sVEGFR‐3‐conditioned medium or luciferase‐conditioned medium was added with 100 ng/mL recombinant human VEGF‐C. The number of LEC with 50% sVEGFR‐3‐conditioned medium (b) was clearly smaller than that with control (a). The cells were counted by colorimetric assay 48 h after plating. Each bar represents the mean ± SD. (*P < 0.01) (c).

    Article Snippet: Human neonatal dermal lymphatic endothelial cells (LEC) were purchased from AngioBio (Del Mar, CA, USA) and maintained in EGM‐MV2 BulletKit (Cambrex, East Rutherford, NJ, USA) supplemented with 10% inactivated FCS at 37°C in a 5% CO 2 atmosphere.

    Techniques: Expressing, Luciferase, Recombinant, Colorimetric Assay

    A , Prostatic LEC tube length at 4.5 hours post VEGF-C treatment was quantified using ImageJ. VEGF-C significantly increased the number of tubes formed compared to vehicle control. Data expressed as mean±s.e.m., n = 3, *** P <0.001 using One-way ANOVA, Bonferroni post-analysis. B , Western blotting analysis of VEGFR-2 and VEGFR-3 expression in lung, neonatal dermis and prostate LECs. β-tubulin was used as a loading control.

    Journal: PLoS ONE

    Article Title: Vascular Endothelial Growth Factor Receptor-3 Directly Interacts with Phosphatidylinositol 3-Kinase to Regulate Lymphangiogenesis

    doi: 10.1371/journal.pone.0039558

    Figure Lengend Snippet: A , Prostatic LEC tube length at 4.5 hours post VEGF-C treatment was quantified using ImageJ. VEGF-C significantly increased the number of tubes formed compared to vehicle control. Data expressed as mean±s.e.m., n = 3, *** P <0.001 using One-way ANOVA, Bonferroni post-analysis. B , Western blotting analysis of VEGFR-2 and VEGFR-3 expression in lung, neonatal dermis and prostate LECs. β-tubulin was used as a loading control.

    Article Snippet: Primary neonatal human dermal LECs and primary human lung LECs were purchased from Lonza (Switzerland) and maintained in EGMTM-2 MV medium (Lonza).

    Techniques: Control, Western Blot, Expressing