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human osteoblast cell line hfob1 19  (ATCC)


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    Structured Review

    ATCC human osteoblast cell line hfob1 19
    a , c Representative brightfield images <t>of</t> <t>hFOB1.19</t> spheroids after 2 and 5 days of exposure to PFOA, respectively. Spheroids exposed to 0.02% of vehicle (DMSO) were used as the control. Images were obtained using the Light Lionheart FX Microscope. Scale bar = 200 μm (magnification 10×). b , d Morphological parameters of hFOB1.19 spheroids after 2 and 5 days of exposure to PFOA, respectively. ImageJ software determined area, solidity, circularity, and roundness after 2 and 5 days of exposure to different PFOA concentrations ( n = 31–40), individual biological replicates. P values indicate the results of comparisons between each PFOA-treated group and the control group. Values of p < 0.05 are considered statistically significant.
    Human Osteoblast Cell Line Hfob1 19, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 939 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human osteoblast cell line hfob1 19/product/ATCC
    Average 98 stars, based on 939 article reviews
    human osteoblast cell line hfob1 19 - by Bioz Stars, 2026-03
    98/100 stars

    Images

    1) Product Images from "Unveiling the toxic effects of perfluorooctanoic acid on osteoblast function and extracellular matrix deposition using 2D and 3D models"

    Article Title: Unveiling the toxic effects of perfluorooctanoic acid on osteoblast function and extracellular matrix deposition using 2D and 3D models

    Journal: Cell Death Discovery

    doi: 10.1038/s41420-025-02863-5

    a , c Representative brightfield images of hFOB1.19 spheroids after 2 and 5 days of exposure to PFOA, respectively. Spheroids exposed to 0.02% of vehicle (DMSO) were used as the control. Images were obtained using the Light Lionheart FX Microscope. Scale bar = 200 μm (magnification 10×). b , d Morphological parameters of hFOB1.19 spheroids after 2 and 5 days of exposure to PFOA, respectively. ImageJ software determined area, solidity, circularity, and roundness after 2 and 5 days of exposure to different PFOA concentrations ( n = 31–40), individual biological replicates. P values indicate the results of comparisons between each PFOA-treated group and the control group. Values of p < 0.05 are considered statistically significant.
    Figure Legend Snippet: a , c Representative brightfield images of hFOB1.19 spheroids after 2 and 5 days of exposure to PFOA, respectively. Spheroids exposed to 0.02% of vehicle (DMSO) were used as the control. Images were obtained using the Light Lionheart FX Microscope. Scale bar = 200 μm (magnification 10×). b , d Morphological parameters of hFOB1.19 spheroids after 2 and 5 days of exposure to PFOA, respectively. ImageJ software determined area, solidity, circularity, and roundness after 2 and 5 days of exposure to different PFOA concentrations ( n = 31–40), individual biological replicates. P values indicate the results of comparisons between each PFOA-treated group and the control group. Values of p < 0.05 are considered statistically significant.

    Techniques Used: Control, Microscopy, Software

    Western blot analysis of oxidative stress marker expression, a (60 kDa) CAT and b (96 kDa) NRF2 for 2D ( n = 5 biological replicates). c – e CAT levels in hFOB1.19 spheroids exposed to different PFOA concentrations for 2 days ( c ) and 5 days ( e ). NRF2 levels in hFOB1.19 spheroids exposed to different PFOA concentrations for 2 days ( d ) and 5 days ( f ) ( n = 3–4 individual biological replicates). P values indicate the results of comparisons between each PFOA-treated group and the control group. Values of p < 0.05 are considered statistically significant.
    Figure Legend Snippet: Western blot analysis of oxidative stress marker expression, a (60 kDa) CAT and b (96 kDa) NRF2 for 2D ( n = 5 biological replicates). c – e CAT levels in hFOB1.19 spheroids exposed to different PFOA concentrations for 2 days ( c ) and 5 days ( e ). NRF2 levels in hFOB1.19 spheroids exposed to different PFOA concentrations for 2 days ( d ) and 5 days ( f ) ( n = 3–4 individual biological replicates). P values indicate the results of comparisons between each PFOA-treated group and the control group. Values of p < 0.05 are considered statistically significant.

    Techniques Used: Western Blot, Marker, Expressing, Control

    Western blot analysis of COL1A2 and CB1 levels. a , b (120 kDa) COL1A2 and (53 kDa) CB1 respectively for 2D ( n = 5 individual biological replicates). c – e Degraded COL1A2 (60 kDa) levels in hFOB1.19 spheroids exposed to different PFOA concentrations for 2 and 5 days, respectively. d , f CB1 levels in hFOB1.19 spheroids exposed to different PFOA concentrations for 2 and 5 days, respectively ( n = 3–4 individual biological replicates). P values indicate the results of comparisons between each PFOA-treated group and the control group. Values of p < 0.05 are considered statistically significant. g Localization of CB1 on the osteoblast membrane on the spheroid surface. Scale bar: 20 μm. Image captured using confocal microscope LSM 800 (Zeiss) (40×).
    Figure Legend Snippet: Western blot analysis of COL1A2 and CB1 levels. a , b (120 kDa) COL1A2 and (53 kDa) CB1 respectively for 2D ( n = 5 individual biological replicates). c – e Degraded COL1A2 (60 kDa) levels in hFOB1.19 spheroids exposed to different PFOA concentrations for 2 and 5 days, respectively. d , f CB1 levels in hFOB1.19 spheroids exposed to different PFOA concentrations for 2 and 5 days, respectively ( n = 3–4 individual biological replicates). P values indicate the results of comparisons between each PFOA-treated group and the control group. Values of p < 0.05 are considered statistically significant. g Localization of CB1 on the osteoblast membrane on the spheroid surface. Scale bar: 20 μm. Image captured using confocal microscope LSM 800 (Zeiss) (40×).

    Techniques Used: Western Blot, Control, Membrane, Microscopy



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    a , c Representative brightfield images <t>of</t> <t>hFOB1.19</t> spheroids after 2 and 5 days of exposure to PFOA, respectively. Spheroids exposed to 0.02% of vehicle (DMSO) were used as the control. Images were obtained using the Light Lionheart FX Microscope. Scale bar = 200 μm (magnification 10×). b , d Morphological parameters of hFOB1.19 spheroids after 2 and 5 days of exposure to PFOA, respectively. ImageJ software determined area, solidity, circularity, and roundness after 2 and 5 days of exposure to different PFOA concentrations ( n = 31–40), individual biological replicates. P values indicate the results of comparisons between each PFOA-treated group and the control group. Values of p < 0.05 are considered statistically significant.
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    a , c Representative brightfield images <t>of</t> <t>hFOB1.19</t> spheroids after 2 and 5 days of exposure to PFOA, respectively. Spheroids exposed to 0.02% of vehicle (DMSO) were used as the control. Images were obtained using the Light Lionheart FX Microscope. Scale bar = 200 μm (magnification 10×). b , d Morphological parameters of hFOB1.19 spheroids after 2 and 5 days of exposure to PFOA, respectively. ImageJ software determined area, solidity, circularity, and roundness after 2 and 5 days of exposure to different PFOA concentrations ( n = 31–40), individual biological replicates. P values indicate the results of comparisons between each PFOA-treated group and the control group. Values of p < 0.05 are considered statistically significant.
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    a , c Representative brightfield images <t>of</t> <t>hFOB1.19</t> spheroids after 2 and 5 days of exposure to PFOA, respectively. Spheroids exposed to 0.02% of vehicle (DMSO) were used as the control. Images were obtained using the Light Lionheart FX Microscope. Scale bar = 200 μm (magnification 10×). b , d Morphological parameters of hFOB1.19 spheroids after 2 and 5 days of exposure to PFOA, respectively. ImageJ software determined area, solidity, circularity, and roundness after 2 and 5 days of exposure to different PFOA concentrations ( n = 31–40), individual biological replicates. P values indicate the results of comparisons between each PFOA-treated group and the control group. Values of p < 0.05 are considered statistically significant.
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    a , c Representative brightfield images <t>of</t> <t>hFOB1.19</t> spheroids after 2 and 5 days of exposure to PFOA, respectively. Spheroids exposed to 0.02% of vehicle (DMSO) were used as the control. Images were obtained using the Light Lionheart FX Microscope. Scale bar = 200 μm (magnification 10×). b , d Morphological parameters of hFOB1.19 spheroids after 2 and 5 days of exposure to PFOA, respectively. ImageJ software determined area, solidity, circularity, and roundness after 2 and 5 days of exposure to different PFOA concentrations ( n = 31–40), individual biological replicates. P values indicate the results of comparisons between each PFOA-treated group and the control group. Values of p < 0.05 are considered statistically significant.
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    Image Search Results


    a , c Representative brightfield images of hFOB1.19 spheroids after 2 and 5 days of exposure to PFOA, respectively. Spheroids exposed to 0.02% of vehicle (DMSO) were used as the control. Images were obtained using the Light Lionheart FX Microscope. Scale bar = 200 μm (magnification 10×). b , d Morphological parameters of hFOB1.19 spheroids after 2 and 5 days of exposure to PFOA, respectively. ImageJ software determined area, solidity, circularity, and roundness after 2 and 5 days of exposure to different PFOA concentrations ( n = 31–40), individual biological replicates. P values indicate the results of comparisons between each PFOA-treated group and the control group. Values of p < 0.05 are considered statistically significant.

    Journal: Cell Death Discovery

    Article Title: Unveiling the toxic effects of perfluorooctanoic acid on osteoblast function and extracellular matrix deposition using 2D and 3D models

    doi: 10.1038/s41420-025-02863-5

    Figure Lengend Snippet: a , c Representative brightfield images of hFOB1.19 spheroids after 2 and 5 days of exposure to PFOA, respectively. Spheroids exposed to 0.02% of vehicle (DMSO) were used as the control. Images were obtained using the Light Lionheart FX Microscope. Scale bar = 200 μm (magnification 10×). b , d Morphological parameters of hFOB1.19 spheroids after 2 and 5 days of exposure to PFOA, respectively. ImageJ software determined area, solidity, circularity, and roundness after 2 and 5 days of exposure to different PFOA concentrations ( n = 31–40), individual biological replicates. P values indicate the results of comparisons between each PFOA-treated group and the control group. Values of p < 0.05 are considered statistically significant.

    Article Snippet: The human osteoblast cell line hFOB1.19 (ATCC CRL-11372) was obtained from the American Type Culture Collection (ATCC, USA) in March 2021.

    Techniques: Control, Microscopy, Software

    Western blot analysis of oxidative stress marker expression, a (60 kDa) CAT and b (96 kDa) NRF2 for 2D ( n = 5 biological replicates). c – e CAT levels in hFOB1.19 spheroids exposed to different PFOA concentrations for 2 days ( c ) and 5 days ( e ). NRF2 levels in hFOB1.19 spheroids exposed to different PFOA concentrations for 2 days ( d ) and 5 days ( f ) ( n = 3–4 individual biological replicates). P values indicate the results of comparisons between each PFOA-treated group and the control group. Values of p < 0.05 are considered statistically significant.

    Journal: Cell Death Discovery

    Article Title: Unveiling the toxic effects of perfluorooctanoic acid on osteoblast function and extracellular matrix deposition using 2D and 3D models

    doi: 10.1038/s41420-025-02863-5

    Figure Lengend Snippet: Western blot analysis of oxidative stress marker expression, a (60 kDa) CAT and b (96 kDa) NRF2 for 2D ( n = 5 biological replicates). c – e CAT levels in hFOB1.19 spheroids exposed to different PFOA concentrations for 2 days ( c ) and 5 days ( e ). NRF2 levels in hFOB1.19 spheroids exposed to different PFOA concentrations for 2 days ( d ) and 5 days ( f ) ( n = 3–4 individual biological replicates). P values indicate the results of comparisons between each PFOA-treated group and the control group. Values of p < 0.05 are considered statistically significant.

    Article Snippet: The human osteoblast cell line hFOB1.19 (ATCC CRL-11372) was obtained from the American Type Culture Collection (ATCC, USA) in March 2021.

    Techniques: Western Blot, Marker, Expressing, Control

    Western blot analysis of COL1A2 and CB1 levels. a , b (120 kDa) COL1A2 and (53 kDa) CB1 respectively for 2D ( n = 5 individual biological replicates). c – e Degraded COL1A2 (60 kDa) levels in hFOB1.19 spheroids exposed to different PFOA concentrations for 2 and 5 days, respectively. d , f CB1 levels in hFOB1.19 spheroids exposed to different PFOA concentrations for 2 and 5 days, respectively ( n = 3–4 individual biological replicates). P values indicate the results of comparisons between each PFOA-treated group and the control group. Values of p < 0.05 are considered statistically significant. g Localization of CB1 on the osteoblast membrane on the spheroid surface. Scale bar: 20 μm. Image captured using confocal microscope LSM 800 (Zeiss) (40×).

    Journal: Cell Death Discovery

    Article Title: Unveiling the toxic effects of perfluorooctanoic acid on osteoblast function and extracellular matrix deposition using 2D and 3D models

    doi: 10.1038/s41420-025-02863-5

    Figure Lengend Snippet: Western blot analysis of COL1A2 and CB1 levels. a , b (120 kDa) COL1A2 and (53 kDa) CB1 respectively for 2D ( n = 5 individual biological replicates). c – e Degraded COL1A2 (60 kDa) levels in hFOB1.19 spheroids exposed to different PFOA concentrations for 2 and 5 days, respectively. d , f CB1 levels in hFOB1.19 spheroids exposed to different PFOA concentrations for 2 and 5 days, respectively ( n = 3–4 individual biological replicates). P values indicate the results of comparisons between each PFOA-treated group and the control group. Values of p < 0.05 are considered statistically significant. g Localization of CB1 on the osteoblast membrane on the spheroid surface. Scale bar: 20 μm. Image captured using confocal microscope LSM 800 (Zeiss) (40×).

    Article Snippet: The human osteoblast cell line hFOB1.19 (ATCC CRL-11372) was obtained from the American Type Culture Collection (ATCC, USA) in March 2021.

    Techniques: Western Blot, Control, Membrane, Microscopy