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primary human retinal microvascular endothelial cells (hrmecs)  (DS Pharma Biomedical)

 
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    Structured Review

    DS Pharma Biomedical primary human retinal microvascular endothelial cells (hrmecs)
    Primary Human Retinal Microvascular Endothelial Cells (Hrmecs), supplied by DS Pharma Biomedical, 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/result/primary human retinal microvascular endothelial cells (hrmecs)/product/DS Pharma Biomedical
    Average 90 stars, based on 1 article reviews
    primary human retinal microvascular endothelial cells (hrmecs) - by Bioz Stars, 2026-03
    90/100 stars

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    Cell Systems Corporation primary human retinal microvascular endothelial cells (hrmecs)
    a Effect of AIBP and HDL 3 on lipid rafts of <t>HRMECs.</t> Cells were stained for lipid rafts (green, D4-EGFP) and nuclei (blue, DAPI) after preincubation with control media, AIBP, HDL 3 , or AIBP plus HDL 3 . b Quantification of the area of lipid rafts per cell. N = 92, 54, 70, and 86 cells for control, AIBP, HDL 3 , and AIBP + HDL 3 , respectively. c Effect of AIBP and HDL 3 on <t>endothelial</t> cell tube formation using the Matrigel-based assay. The total segment length of HRMEC tubes was quantified after various treatments. N = 12, 9, 6, 6, and 6 for control, AIBP, HDL 3 , AIBP + HDL 3 , and MβCD, respectively. Representative images ( d ) and quantification of <t>microvascular</t> sprouting area ( e ) after AIBP treatment. N = 3 explants per group. Data represent mean ± SEM in b , c , e . Statistical analysis was performed by one-way ANOVA with Tukey post hoc analysis ( b , c ) or two-tailed Student’s t -test ( e ).
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    Image Search Results


    a Effect of AIBP and HDL 3 on lipid rafts of HRMECs. Cells were stained for lipid rafts (green, D4-EGFP) and nuclei (blue, DAPI) after preincubation with control media, AIBP, HDL 3 , or AIBP plus HDL 3 . b Quantification of the area of lipid rafts per cell. N = 92, 54, 70, and 86 cells for control, AIBP, HDL 3 , and AIBP + HDL 3 , respectively. c Effect of AIBP and HDL 3 on endothelial cell tube formation using the Matrigel-based assay. The total segment length of HRMEC tubes was quantified after various treatments. N = 12, 9, 6, 6, and 6 for control, AIBP, HDL 3 , AIBP + HDL 3 , and MβCD, respectively. Representative images ( d ) and quantification of microvascular sprouting area ( e ) after AIBP treatment. N = 3 explants per group. Data represent mean ± SEM in b , c , e . Statistical analysis was performed by one-way ANOVA with Tukey post hoc analysis ( b , c ) or two-tailed Student’s t -test ( e ).

    Journal: Communications Biology

    Article Title: Combination of apolipoprotein-A-I/apolipoprotein-A-I binding protein and anti-VEGF treatment overcomes anti-VEGF resistance in choroidal neovascularization in mice

    doi: 10.1038/s42003-020-1113-z

    Figure Lengend Snippet: a Effect of AIBP and HDL 3 on lipid rafts of HRMECs. Cells were stained for lipid rafts (green, D4-EGFP) and nuclei (blue, DAPI) after preincubation with control media, AIBP, HDL 3 , or AIBP plus HDL 3 . b Quantification of the area of lipid rafts per cell. N = 92, 54, 70, and 86 cells for control, AIBP, HDL 3 , and AIBP + HDL 3 , respectively. c Effect of AIBP and HDL 3 on endothelial cell tube formation using the Matrigel-based assay. The total segment length of HRMEC tubes was quantified after various treatments. N = 12, 9, 6, 6, and 6 for control, AIBP, HDL 3 , AIBP + HDL 3 , and MβCD, respectively. Representative images ( d ) and quantification of microvascular sprouting area ( e ) after AIBP treatment. N = 3 explants per group. Data represent mean ± SEM in b , c , e . Statistical analysis was performed by one-way ANOVA with Tukey post hoc analysis ( b , c ) or two-tailed Student’s t -test ( e ).

    Article Snippet: Primary human retinal microvascular endothelial cells (HRMECs) were purchased from Cell Systems Corporation (Kirkland, WA, USA).

    Techniques: Staining, Control, Matrigel Assay, Two Tailed Test

    a Peritoneal macrophage isolated from 1-month, 8-month, and 18-month 57Bl6/J mice were treated with AIBP and apoA-I, and stained with oil red O. b Quantification on the number of lipid droplets per cell in macrophages. N = 25 (control) and 28 (AIBP/apoA-I) for 8-month mice, 43 (control) and 39 (AIBP/apoA-I) for 18-month mice. c Effect of AIBP on old macrophages’ ability to promote angiogenesis of HRMECs. Macrophages (MΦ) isolated from 1-month and 18-month mice were pretreated with different combination of AIBP and apoA-I and co-cultured with HRMECs. d Quantitative analysis of total segment length of tubes of HRMECs in c . N = 7 (without co-culture), 10 (1-month MΦ + control), 6 (1-month MΦ + AIBP/apoA-I), 14 (18-month MΦ + control), and 13 (18-month MΦ + AIBP/apoA-I) fields. Data represent mean ± SEM in b , d . Statistical analysis was performed by two-tailed Student’s t -test ( b ) or one-way ANOVA with Tukey post hoc analysis ( d ). Scale bar, 25 µm in a , 1000 µm in c .

    Journal: Communications Biology

    Article Title: Combination of apolipoprotein-A-I/apolipoprotein-A-I binding protein and anti-VEGF treatment overcomes anti-VEGF resistance in choroidal neovascularization in mice

    doi: 10.1038/s42003-020-1113-z

    Figure Lengend Snippet: a Peritoneal macrophage isolated from 1-month, 8-month, and 18-month 57Bl6/J mice were treated with AIBP and apoA-I, and stained with oil red O. b Quantification on the number of lipid droplets per cell in macrophages. N = 25 (control) and 28 (AIBP/apoA-I) for 8-month mice, 43 (control) and 39 (AIBP/apoA-I) for 18-month mice. c Effect of AIBP on old macrophages’ ability to promote angiogenesis of HRMECs. Macrophages (MΦ) isolated from 1-month and 18-month mice were pretreated with different combination of AIBP and apoA-I and co-cultured with HRMECs. d Quantitative analysis of total segment length of tubes of HRMECs in c . N = 7 (without co-culture), 10 (1-month MΦ + control), 6 (1-month MΦ + AIBP/apoA-I), 14 (18-month MΦ + control), and 13 (18-month MΦ + AIBP/apoA-I) fields. Data represent mean ± SEM in b , d . Statistical analysis was performed by two-tailed Student’s t -test ( b ) or one-way ANOVA with Tukey post hoc analysis ( d ). Scale bar, 25 µm in a , 1000 µm in c .

    Article Snippet: Primary human retinal microvascular endothelial cells (HRMECs) were purchased from Cell Systems Corporation (Kirkland, WA, USA).

    Techniques: Isolation, Staining, Control, Cell Culture, Co-Culture Assay, Two Tailed Test

    a Representative images and quantification of microvascular sprouting area from Naxe −/− and WT adult mouse choroid explants. N = 3 choroid explants for WT , 4 for Naxe −/− mice. b Representative images of CNV lesions labeled by Alexa 568-isolectin on RPE-choroid flatmounts and quantification of CNV areas from Naxe −/− and WT adult mice. N = 33 laser spots per group. c Representative images of CNV lesions and quantification of CNV areas after intravitreal injection of a rabbit anti-AIBP antibody or a control IgG. N = 28 laser spots per group. Scale bar is 20 µm in b and c . Data represent mean ± SEM in a – c . Statistical analysis was performed by two-tailed Student’s t -test.

    Journal: Communications Biology

    Article Title: Combination of apolipoprotein-A-I/apolipoprotein-A-I binding protein and anti-VEGF treatment overcomes anti-VEGF resistance in choroidal neovascularization in mice

    doi: 10.1038/s42003-020-1113-z

    Figure Lengend Snippet: a Representative images and quantification of microvascular sprouting area from Naxe −/− and WT adult mouse choroid explants. N = 3 choroid explants for WT , 4 for Naxe −/− mice. b Representative images of CNV lesions labeled by Alexa 568-isolectin on RPE-choroid flatmounts and quantification of CNV areas from Naxe −/− and WT adult mice. N = 33 laser spots per group. c Representative images of CNV lesions and quantification of CNV areas after intravitreal injection of a rabbit anti-AIBP antibody or a control IgG. N = 28 laser spots per group. Scale bar is 20 µm in b and c . Data represent mean ± SEM in a – c . Statistical analysis was performed by two-tailed Student’s t -test.

    Article Snippet: Primary human retinal microvascular endothelial cells (HRMECs) were purchased from Cell Systems Corporation (Kirkland, WA, USA).

    Techniques: Labeling, Injection, Control, Two Tailed Test