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adult primary human dermal lymphatic endothelial cells hdlecs  (PromoCell)


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    Structured Review

    PromoCell adult primary human dermal lymphatic endothelial cells hdlecs
    (A) PDMS devices fabricated from soft lithography molds assembled onto MatTek glass-bottom culture dishes with integrated removable PDMS rods, and resultant lumen channels following rod removal after collagen polymerization. (B) Schematic showing the lumen seeding arrangement with one lumen seeded with human dermal lymphatic <t>endothelial</t> cells <t>(HdLECs,</t> yellow) to form a biomimetic lymphatic vessel and the adjacent lumen loaded with neutrophils (purple). pHrodo-conjugated bacterial bioparticles (green) are embedded within the surrounding collagen matrix. (C) Representative fluorescence image of a biomimetic lymphatic vessel formed within the collagen matrix.
    Adult Primary Human Dermal Lymphatic Endothelial Cells Hdlecs, supplied by PromoCell, used in various techniques. Bioz Stars score: 97/100, based on 274 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/adult primary human dermal lymphatic endothelial cells hdlecs/product/PromoCell
    Average 97 stars, based on 274 article reviews
    adult primary human dermal lymphatic endothelial cells hdlecs - by Bioz Stars, 2026-05
    97/100 stars

    Images

    1) Product Images from "Lymphatic Endothelial Cells Regulate Neutrophil Phenotypes and Function in a Microphysiological Model of Infection"

    Article Title: Lymphatic Endothelial Cells Regulate Neutrophil Phenotypes and Function in a Microphysiological Model of Infection

    Journal: bioRxiv

    doi: 10.64898/2026.03.24.714048

    (A) PDMS devices fabricated from soft lithography molds assembled onto MatTek glass-bottom culture dishes with integrated removable PDMS rods, and resultant lumen channels following rod removal after collagen polymerization. (B) Schematic showing the lumen seeding arrangement with one lumen seeded with human dermal lymphatic endothelial cells (HdLECs, yellow) to form a biomimetic lymphatic vessel and the adjacent lumen loaded with neutrophils (purple). pHrodo-conjugated bacterial bioparticles (green) are embedded within the surrounding collagen matrix. (C) Representative fluorescence image of a biomimetic lymphatic vessel formed within the collagen matrix.
    Figure Legend Snippet: (A) PDMS devices fabricated from soft lithography molds assembled onto MatTek glass-bottom culture dishes with integrated removable PDMS rods, and resultant lumen channels following rod removal after collagen polymerization. (B) Schematic showing the lumen seeding arrangement with one lumen seeded with human dermal lymphatic endothelial cells (HdLECs, yellow) to form a biomimetic lymphatic vessel and the adjacent lumen loaded with neutrophils (purple). pHrodo-conjugated bacterial bioparticles (green) are embedded within the surrounding collagen matrix. (C) Representative fluorescence image of a biomimetic lymphatic vessel formed within the collagen matrix.

    Techniques Used: Fluorescence



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    PromoCell adult primary human dermal lymphatic endothelial cells hdlecs
    (A) PDMS devices fabricated from soft lithography molds assembled onto MatTek glass-bottom culture dishes with integrated removable PDMS rods, and resultant lumen channels following rod removal after collagen polymerization. (B) Schematic showing the lumen seeding arrangement with one lumen seeded with human dermal lymphatic <t>endothelial</t> cells <t>(HdLECs,</t> yellow) to form a biomimetic lymphatic vessel and the adjacent lumen loaded with neutrophils (purple). pHrodo-conjugated bacterial bioparticles (green) are embedded within the surrounding collagen matrix. (C) Representative fluorescence image of a biomimetic lymphatic vessel formed within the collagen matrix.
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    (A) PDMS devices fabricated from soft lithography molds assembled onto MatTek glass-bottom culture dishes with integrated removable PDMS rods, and resultant lumen channels following rod removal after collagen polymerization. (B) Schematic showing the lumen seeding arrangement with one lumen seeded with human dermal lymphatic <t>endothelial</t> cells <t>(HdLECs,</t> yellow) to form a biomimetic lymphatic vessel and the adjacent lumen loaded with neutrophils (purple). pHrodo-conjugated bacterial bioparticles (green) are embedded within the surrounding collagen matrix. (C) Representative fluorescence image of a biomimetic lymphatic vessel formed within the collagen matrix.
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    PromoCell male primary human dermal lymphatic endothelial cells
    (A) PDMS devices fabricated from soft lithography molds assembled onto MatTek glass-bottom culture dishes with integrated removable PDMS rods, and resultant lumen channels following rod removal after collagen polymerization. (B) Schematic showing the lumen seeding arrangement with one lumen seeded with human dermal lymphatic <t>endothelial</t> cells <t>(HdLECs,</t> yellow) to form a biomimetic lymphatic vessel and the adjacent lumen loaded with neutrophils (purple). pHrodo-conjugated bacterial bioparticles (green) are embedded within the surrounding collagen matrix. (C) Representative fluorescence image of a biomimetic lymphatic vessel formed within the collagen matrix.
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    PromoCell primary human dermal lymphatic endothelial cells lecs
    (A) PDMS devices fabricated from soft lithography molds assembled onto MatTek glass-bottom culture dishes with integrated removable PDMS rods, and resultant lumen channels following rod removal after collagen polymerization. (B) Schematic showing the lumen seeding arrangement with one lumen seeded with human dermal lymphatic <t>endothelial</t> cells <t>(HdLECs,</t> yellow) to form a biomimetic lymphatic vessel and the adjacent lumen loaded with neutrophils (purple). pHrodo-conjugated bacterial bioparticles (green) are embedded within the surrounding collagen matrix. (C) Representative fluorescence image of a biomimetic lymphatic vessel formed within the collagen matrix.
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    PromoCell primary human dermal lymphatic endothelial cells hdlecs
    (A) PDMS devices fabricated from soft lithography molds assembled onto MatTek glass-bottom culture dishes with integrated removable PDMS rods, and resultant lumen channels following rod removal after collagen polymerization. (B) Schematic showing the lumen seeding arrangement with one lumen seeded with human dermal lymphatic <t>endothelial</t> cells <t>(HdLECs,</t> yellow) to form a biomimetic lymphatic vessel and the adjacent lumen loaded with neutrophils (purple). pHrodo-conjugated bacterial bioparticles (green) are embedded within the surrounding collagen matrix. (C) Representative fluorescence image of a biomimetic lymphatic vessel formed within the collagen matrix.
    Primary Human Dermal Lymphatic Endothelial Cells Hdlecs, supplied by PromoCell, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/primary human dermal lymphatic endothelial cells hdlecs/product/PromoCell
    Average 97 stars, based on 1 article reviews
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    97/100 stars
      Buy from Supplier

    94
    Angio-Proteomie dermal primary human lymphatic endothelial cells
    Integration of lymphatic <t>endothelial</t> cells (LEC) increases the biomimicry of a self‐assembled lymphoreticular (LR) model. A) Exemplary histological staining of a human lymph node. Scale bar = 1 mm. Copyright permission has been obtained from Xinxiang Happy Science Co., Ltd. B) Schematic illustration of the layering approach. C) Brightfield image of a self‐assembled LR model. D) Representative H&E staining and E) IF images showing the FRC‐derived ECM marker ER‐TR7 (red), DAPI (blue) and the localization of GFP‐tagged LECs of LR models generated using different layering approaches: FLF (FRCs + GPF‐LECs + FRC), FLFN (FRC + GPF‐LECs + (FRC + naïve CD4 + T cells)), FLFA (FRC + GPF‐LECs + (FRC + activated CD4 + T cells)), FLN (FRC + GPF‐LECs + naïve CD4 + T cells), and FLA (FRC + GPF‐LECs + activated CD4 + T cells). Circles and arrows indicate the compartmentalization within LR models. Semi‐quantification of F) ER‐TR7 expression and G) GFP‐LEC distribution in the LR models generated using the different layering approaches. n = 3. One‐way ANOVA followed with Tukey post‐hoc tests were performed. Mean ± SD. * p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001, ****p ≤ 0.0001. H) IF staining against collagen type 1 and fibronectin as key ECM components of lymphoid tissue in FLFA models. Cell nuclei are counterstained with DAPI (blue). Scale bars = 100 µm.
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    Image Search Results


    (A) PDMS devices fabricated from soft lithography molds assembled onto MatTek glass-bottom culture dishes with integrated removable PDMS rods, and resultant lumen channels following rod removal after collagen polymerization. (B) Schematic showing the lumen seeding arrangement with one lumen seeded with human dermal lymphatic endothelial cells (HdLECs, yellow) to form a biomimetic lymphatic vessel and the adjacent lumen loaded with neutrophils (purple). pHrodo-conjugated bacterial bioparticles (green) are embedded within the surrounding collagen matrix. (C) Representative fluorescence image of a biomimetic lymphatic vessel formed within the collagen matrix.

    Journal: bioRxiv

    Article Title: Lymphatic Endothelial Cells Regulate Neutrophil Phenotypes and Function in a Microphysiological Model of Infection

    doi: 10.64898/2026.03.24.714048

    Figure Lengend Snippet: (A) PDMS devices fabricated from soft lithography molds assembled onto MatTek glass-bottom culture dishes with integrated removable PDMS rods, and resultant lumen channels following rod removal after collagen polymerization. (B) Schematic showing the lumen seeding arrangement with one lumen seeded with human dermal lymphatic endothelial cells (HdLECs, yellow) to form a biomimetic lymphatic vessel and the adjacent lumen loaded with neutrophils (purple). pHrodo-conjugated bacterial bioparticles (green) are embedded within the surrounding collagen matrix. (C) Representative fluorescence image of a biomimetic lymphatic vessel formed within the collagen matrix.

    Article Snippet: Adult primary human dermal lymphatic endothelial cells (HdLECs) were purchased from PromoCell (C-12217).

    Techniques: Fluorescence

    Integration of lymphatic endothelial cells (LEC) increases the biomimicry of a self‐assembled lymphoreticular (LR) model. A) Exemplary histological staining of a human lymph node. Scale bar = 1 mm. Copyright permission has been obtained from Xinxiang Happy Science Co., Ltd. B) Schematic illustration of the layering approach. C) Brightfield image of a self‐assembled LR model. D) Representative H&E staining and E) IF images showing the FRC‐derived ECM marker ER‐TR7 (red), DAPI (blue) and the localization of GFP‐tagged LECs of LR models generated using different layering approaches: FLF (FRCs + GPF‐LECs + FRC), FLFN (FRC + GPF‐LECs + (FRC + naïve CD4 + T cells)), FLFA (FRC + GPF‐LECs + (FRC + activated CD4 + T cells)), FLN (FRC + GPF‐LECs + naïve CD4 + T cells), and FLA (FRC + GPF‐LECs + activated CD4 + T cells). Circles and arrows indicate the compartmentalization within LR models. Semi‐quantification of F) ER‐TR7 expression and G) GFP‐LEC distribution in the LR models generated using the different layering approaches. n = 3. One‐way ANOVA followed with Tukey post‐hoc tests were performed. Mean ± SD. * p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001, ****p ≤ 0.0001. H) IF staining against collagen type 1 and fibronectin as key ECM components of lymphoid tissue in FLFA models. Cell nuclei are counterstained with DAPI (blue). Scale bars = 100 µm.

    Journal: Advanced Healthcare Materials

    Article Title: A Human‐Based Skin‐Lymphoreticular Model‐on‐Chip to Emulate Inflammatory Skin Conditions

    doi: 10.1002/adhm.202503170

    Figure Lengend Snippet: Integration of lymphatic endothelial cells (LEC) increases the biomimicry of a self‐assembled lymphoreticular (LR) model. A) Exemplary histological staining of a human lymph node. Scale bar = 1 mm. Copyright permission has been obtained from Xinxiang Happy Science Co., Ltd. B) Schematic illustration of the layering approach. C) Brightfield image of a self‐assembled LR model. D) Representative H&E staining and E) IF images showing the FRC‐derived ECM marker ER‐TR7 (red), DAPI (blue) and the localization of GFP‐tagged LECs of LR models generated using different layering approaches: FLF (FRCs + GPF‐LECs + FRC), FLFN (FRC + GPF‐LECs + (FRC + naïve CD4 + T cells)), FLFA (FRC + GPF‐LECs + (FRC + activated CD4 + T cells)), FLN (FRC + GPF‐LECs + naïve CD4 + T cells), and FLA (FRC + GPF‐LECs + activated CD4 + T cells). Circles and arrows indicate the compartmentalization within LR models. Semi‐quantification of F) ER‐TR7 expression and G) GFP‐LEC distribution in the LR models generated using the different layering approaches. n = 3. One‐way ANOVA followed with Tukey post‐hoc tests were performed. Mean ± SD. * p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001, ****p ≤ 0.0001. H) IF staining against collagen type 1 and fibronectin as key ECM components of lymphoid tissue in FLFA models. Cell nuclei are counterstained with DAPI (blue). Scale bars = 100 µm.

    Article Snippet: Green fluorescent protein‐expressing dermal primary human lymphatic endothelial cells (GFP – LECs) (cAP‐0003GFP, male donor) and the Quick Coating Solution (cAP‐01) were purchased from Angio‐Proteomie.

    Techniques: Staining, Derivative Assay, Marker, Generated, Expressing