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human primary retinal pigment epithelial cells  (ATCC)


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    Structured Review

    ATCC human primary retinal pigment epithelial cells
    Human Primary Retinal Pigment Epithelial Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 571 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human primary retinal pigment epithelial cells/product/ATCC
    Average 97 stars, based on 571 article reviews
    human primary retinal pigment epithelial cells - by Bioz Stars, 2026-02
    97/100 stars

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    ATCC human primary retinal pigment epithelial cells
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    ATCC human eye retinal pigment epithelial cells
    The cell viability of ARPE-19 human retinal <t>epithelial</t> cells treated with fruit (up panel) and leaf (down panel) extracts at varying concentrations for 24 h and 48 h. Extracts were obtained from olives grown at different distances from the Yatağan TPP, Deştin Village (farthest location), Central (middle location), and Thermal (Şahinler Village - closest location). Values represent mean ± SEM ( n = 3). * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001.
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    ATCC wild type human retinal pigmented epithelial cells
    A. <t>Wild</t> <t>type</t> RPE1 cells immunostained against Sec31A. B. Scatter plot of number of Sec31A positive structures in wild type RPE1 cells, colour coded by experimental repeat, n = 32 cells. C. HaloTag-Sec23A-RPE1 cells dyed with JFX650-HaloTag ligand (green) and co-stained using an antibody directed against Sec31A (purple). Inset highlights tight colocalization of HaloTag-Sec23A fusion protein and endogenous Sec31A. D. Example cryo-fluorescence wide field image of HaloTag-Sec23A-RPE1 cells grown on grids stained with Oregon Green HaloTag ligand before and after milling. HaloTag-Sec23A displays a punctate staining pattern throughout the cytoplasm and is concentrated at the perinuclear region. The red box in the left panel indicates the digitally magnified region in the other panels which show cryo-fluorescence before (middle panel) and after (right panel) milling. Four cells are indicated by green dotted outlines. Blue arrow heads indicate clusters of fluorescent fiducials. Green arrows indicate fluorescent puncta visible both before and after milling. Scale bars: 10um, inset in panel C: 1um.
    Wild Type Human Retinal Pigmented Epithelial Cells, supplied by ATCC, 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/wild type human retinal pigmented epithelial cells/product/ATCC
    Average 97 stars, based on 1 article reviews
    wild type human retinal pigmented epithelial cells - by Bioz Stars, 2026-02
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    ATCC human retinal pigmented epithelial cells
    A. <t>Wild</t> <t>type</t> RPE1 cells immunostained against Sec31A. B. Scatter plot of number of Sec31A positive structures in wild type RPE1 cells, colour coded by experimental repeat, n = 32 cells. C. HaloTag-Sec23A-RPE1 cells dyed with JFX650-HaloTag ligand (green) and co-stained using an antibody directed against Sec31A (purple). Inset highlights tight colocalization of HaloTag-Sec23A fusion protein and endogenous Sec31A. D. Example cryo-fluorescence wide field image of HaloTag-Sec23A-RPE1 cells grown on grids stained with Oregon Green HaloTag ligand before and after milling. HaloTag-Sec23A displays a punctate staining pattern throughout the cytoplasm and is concentrated at the perinuclear region. The red box in the left panel indicates the digitally magnified region in the other panels which show cryo-fluorescence before (middle panel) and after (right panel) milling. Four cells are indicated by green dotted outlines. Blue arrow heads indicate clusters of fluorescent fiducials. Green arrows indicate fluorescent puncta visible both before and after milling. Scale bars: 10um, inset in panel C: 1um.
    Human Retinal Pigmented Epithelial Cells, supplied by ATCC, 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/human retinal pigmented epithelial cells/product/ATCC
    Average 97 stars, based on 1 article reviews
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    Angio-Proteomie primary human pigmented epithelial cells hrpes
    A. <t>Wild</t> <t>type</t> RPE1 cells immunostained against Sec31A. B. Scatter plot of number of Sec31A positive structures in wild type RPE1 cells, colour coded by experimental repeat, n = 32 cells. C. HaloTag-Sec23A-RPE1 cells dyed with JFX650-HaloTag ligand (green) and co-stained using an antibody directed against Sec31A (purple). Inset highlights tight colocalization of HaloTag-Sec23A fusion protein and endogenous Sec31A. D. Example cryo-fluorescence wide field image of HaloTag-Sec23A-RPE1 cells grown on grids stained with Oregon Green HaloTag ligand before and after milling. HaloTag-Sec23A displays a punctate staining pattern throughout the cytoplasm and is concentrated at the perinuclear region. The red box in the left panel indicates the digitally magnified region in the other panels which show cryo-fluorescence before (middle panel) and after (right panel) milling. Four cells are indicated by green dotted outlines. Blue arrow heads indicate clusters of fluorescent fiducials. Green arrows indicate fluorescent puncta visible both before and after milling. Scale bars: 10um, inset in panel C: 1um.
    Primary Human Pigmented Epithelial Cells Hrpes, supplied by Angio-Proteomie, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    The cell viability of ARPE-19 human retinal epithelial cells treated with fruit (up panel) and leaf (down panel) extracts at varying concentrations for 24 h and 48 h. Extracts were obtained from olives grown at different distances from the Yatağan TPP, Deştin Village (farthest location), Central (middle location), and Thermal (Şahinler Village - closest location). Values represent mean ± SEM ( n = 3). * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001.

    Journal: Scientific Reports

    Article Title: Thermal power plant proximity alters Olive composition and induces cytotoxicity in human cells

    doi: 10.1038/s41598-025-18066-y

    Figure Lengend Snippet: The cell viability of ARPE-19 human retinal epithelial cells treated with fruit (up panel) and leaf (down panel) extracts at varying concentrations for 24 h and 48 h. Extracts were obtained from olives grown at different distances from the Yatağan TPP, Deştin Village (farthest location), Central (middle location), and Thermal (Şahinler Village - closest location). Values represent mean ± SEM ( n = 3). * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001.

    Article Snippet: The cells included MCF10A (ATCC, CRL-10317TM) human mammary gland epithelial cells, ARPE-19 (ATCC, CRL-2302TM) human eye retinal pigment epithelial cells, HUVEC (ATCC, CRL-1730TM) primary human umbilical vein endothelial cells, and BEAS-2B (ATCC, CRL-3588TM) epithelial cells isolated from normal human bronchial epithelium.

    Techniques:

    The cell viability of MCF10A human breast epithelial cells treated with fruit (up panel) and leaf (down panel) extracts at varying concentrations for 24 h and 48 h. Extracts were obtained from olives grown at different distances from the Yatağan TPP, Deştin Village (farthest location), Central (middle location), and Thermal (Şahinler Village - closest location). Values represent mean ± SEM ( n = 3). * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001.

    Journal: Scientific Reports

    Article Title: Thermal power plant proximity alters Olive composition and induces cytotoxicity in human cells

    doi: 10.1038/s41598-025-18066-y

    Figure Lengend Snippet: The cell viability of MCF10A human breast epithelial cells treated with fruit (up panel) and leaf (down panel) extracts at varying concentrations for 24 h and 48 h. Extracts were obtained from olives grown at different distances from the Yatağan TPP, Deştin Village (farthest location), Central (middle location), and Thermal (Şahinler Village - closest location). Values represent mean ± SEM ( n = 3). * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001.

    Article Snippet: The cells included MCF10A (ATCC, CRL-10317TM) human mammary gland epithelial cells, ARPE-19 (ATCC, CRL-2302TM) human eye retinal pigment epithelial cells, HUVEC (ATCC, CRL-1730TM) primary human umbilical vein endothelial cells, and BEAS-2B (ATCC, CRL-3588TM) epithelial cells isolated from normal human bronchial epithelium.

    Techniques:

    The cell viability of BEAS-2B human bronchial epithelial cells treated with fruit (up panel) and leaf (down panel) extracts at varying concentrations for 24 h and 48 h. Extracts were obtained from olives grown at different distances from the Yatağan TPP, Deştin Village (farthest location), Central (middle location), and Thermal (Şahinler Village - closest location). Representative cells after the MTT assay are given after leaf extracts for 48 h (images taken by 5x objective of Zeiss AxioVert inverted microscope). Values represent mean ± SEM ( n = 3). * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001.

    Journal: Scientific Reports

    Article Title: Thermal power plant proximity alters Olive composition and induces cytotoxicity in human cells

    doi: 10.1038/s41598-025-18066-y

    Figure Lengend Snippet: The cell viability of BEAS-2B human bronchial epithelial cells treated with fruit (up panel) and leaf (down panel) extracts at varying concentrations for 24 h and 48 h. Extracts were obtained from olives grown at different distances from the Yatağan TPP, Deştin Village (farthest location), Central (middle location), and Thermal (Şahinler Village - closest location). Representative cells after the MTT assay are given after leaf extracts for 48 h (images taken by 5x objective of Zeiss AxioVert inverted microscope). Values represent mean ± SEM ( n = 3). * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001.

    Article Snippet: The cells included MCF10A (ATCC, CRL-10317TM) human mammary gland epithelial cells, ARPE-19 (ATCC, CRL-2302TM) human eye retinal pigment epithelial cells, HUVEC (ATCC, CRL-1730TM) primary human umbilical vein endothelial cells, and BEAS-2B (ATCC, CRL-3588TM) epithelial cells isolated from normal human bronchial epithelium.

    Techniques: MTT Assay, Inverted Microscopy

    A. Wild type RPE1 cells immunostained against Sec31A. B. Scatter plot of number of Sec31A positive structures in wild type RPE1 cells, colour coded by experimental repeat, n = 32 cells. C. HaloTag-Sec23A-RPE1 cells dyed with JFX650-HaloTag ligand (green) and co-stained using an antibody directed against Sec31A (purple). Inset highlights tight colocalization of HaloTag-Sec23A fusion protein and endogenous Sec31A. D. Example cryo-fluorescence wide field image of HaloTag-Sec23A-RPE1 cells grown on grids stained with Oregon Green HaloTag ligand before and after milling. HaloTag-Sec23A displays a punctate staining pattern throughout the cytoplasm and is concentrated at the perinuclear region. The red box in the left panel indicates the digitally magnified region in the other panels which show cryo-fluorescence before (middle panel) and after (right panel) milling. Four cells are indicated by green dotted outlines. Blue arrow heads indicate clusters of fluorescent fiducials. Green arrows indicate fluorescent puncta visible both before and after milling. Scale bars: 10um, inset in panel C: 1um.

    Journal: bioRxiv

    Article Title: Multi-scale Molecular Imaging of Human Cells reveals COPI and COPII Vesicles at ER Exit Sites

    doi: 10.1101/2025.07.29.667472

    Figure Lengend Snippet: A. Wild type RPE1 cells immunostained against Sec31A. B. Scatter plot of number of Sec31A positive structures in wild type RPE1 cells, colour coded by experimental repeat, n = 32 cells. C. HaloTag-Sec23A-RPE1 cells dyed with JFX650-HaloTag ligand (green) and co-stained using an antibody directed against Sec31A (purple). Inset highlights tight colocalization of HaloTag-Sec23A fusion protein and endogenous Sec31A. D. Example cryo-fluorescence wide field image of HaloTag-Sec23A-RPE1 cells grown on grids stained with Oregon Green HaloTag ligand before and after milling. HaloTag-Sec23A displays a punctate staining pattern throughout the cytoplasm and is concentrated at the perinuclear region. The red box in the left panel indicates the digitally magnified region in the other panels which show cryo-fluorescence before (middle panel) and after (right panel) milling. Four cells are indicated by green dotted outlines. Blue arrow heads indicate clusters of fluorescent fiducials. Green arrows indicate fluorescent puncta visible both before and after milling. Scale bars: 10um, inset in panel C: 1um.

    Article Snippet: Wild type human retinal pigmented epithelial cells (RPE-1) were obtained from ATCC and were cultured in DMEM/F12 (ThermoFisher Scientific) plus 10% FBS, L-glutamine and 1% Pen/Strep (Bio Basic).

    Techniques: Staining, Fluorescence