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normal human fetal osteoblast cell line  (ATCC)


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    Structured Review

    ATCC normal human fetal osteoblast cell line
    Cytotoxicity assessment of biomaterials enriched with CAPE derivatives on hFOB 1.19 <t>osteoblasts.</t> ( a ) MTT assay conducted by using 24 h extracts of the biomaterials after 48 h cell culture (PS medium—polystyrene extract served as negative control of cytotoxicity; * statistically significant results compared to PS medium, # statistically significant results compared to mat_control, $ statistically significant results compared to mat_ 1d _L, ^ statistically significant results compared to mat_ 1a _L, p < 0.05, One-way ANOVA followed by Tukey’s test); ( b ) confocal laser scanning microscope images showing live/dead staining of cells cultured on the surface of biomaterials for 48 h (Nomarski contrast was applied to show biomaterial microstructure; viable cells—green fluorescence; dead cells—red fluorescence; magnified 100×, scale bar = 200 µm).
    Normal Human Fetal Osteoblast Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 936 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/normal human fetal osteoblast cell line/product/ATCC
    Average 98 stars, based on 936 article reviews
    normal human fetal osteoblast cell line - by Bioz Stars, 2026-02
    98/100 stars

    Images

    1) Product Images from "CAPE Derivatives as Potent Agents for Induction of Osteogenic Differentiation in DPSCs and Biomaterial Development"

    Article Title: CAPE Derivatives as Potent Agents for Induction of Osteogenic Differentiation in DPSCs and Biomaterial Development

    Journal: Biomedicines

    doi: 10.3390/biomedicines13123039

    Cytotoxicity assessment of biomaterials enriched with CAPE derivatives on hFOB 1.19 osteoblasts. ( a ) MTT assay conducted by using 24 h extracts of the biomaterials after 48 h cell culture (PS medium—polystyrene extract served as negative control of cytotoxicity; * statistically significant results compared to PS medium, # statistically significant results compared to mat_control, $ statistically significant results compared to mat_ 1d _L, ^ statistically significant results compared to mat_ 1a _L, p < 0.05, One-way ANOVA followed by Tukey’s test); ( b ) confocal laser scanning microscope images showing live/dead staining of cells cultured on the surface of biomaterials for 48 h (Nomarski contrast was applied to show biomaterial microstructure; viable cells—green fluorescence; dead cells—red fluorescence; magnified 100×, scale bar = 200 µm).
    Figure Legend Snippet: Cytotoxicity assessment of biomaterials enriched with CAPE derivatives on hFOB 1.19 osteoblasts. ( a ) MTT assay conducted by using 24 h extracts of the biomaterials after 48 h cell culture (PS medium—polystyrene extract served as negative control of cytotoxicity; * statistically significant results compared to PS medium, # statistically significant results compared to mat_control, $ statistically significant results compared to mat_ 1d _L, ^ statistically significant results compared to mat_ 1a _L, p < 0.05, One-way ANOVA followed by Tukey’s test); ( b ) confocal laser scanning microscope images showing live/dead staining of cells cultured on the surface of biomaterials for 48 h (Nomarski contrast was applied to show biomaterial microstructure; viable cells—green fluorescence; dead cells—red fluorescence; magnified 100×, scale bar = 200 µm).

    Techniques Used: MTT Assay, Cell Culture, Negative Control, Control, Laser-Scanning Microscopy, Staining, Fluorescence



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    ATCC normal human fetal osteoblast cell line
    Cytotoxicity assessment of biomaterials enriched with CAPE derivatives on hFOB 1.19 <t>osteoblasts.</t> ( a ) MTT assay conducted by using 24 h extracts of the biomaterials after 48 h cell culture (PS medium—polystyrene extract served as negative control of cytotoxicity; * statistically significant results compared to PS medium, # statistically significant results compared to mat_control, $ statistically significant results compared to mat_ 1d _L, ^ statistically significant results compared to mat_ 1a _L, p < 0.05, One-way ANOVA followed by Tukey’s test); ( b ) confocal laser scanning microscope images showing live/dead staining of cells cultured on the surface of biomaterials for 48 h (Nomarski contrast was applied to show biomaterial microstructure; viable cells—green fluorescence; dead cells—red fluorescence; magnified 100×, scale bar = 200 µm).
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    Expression and biological functions on growth of SFXN4 and SQOR in osteosarcoma. (A) SFXN4 and SQOR expression in para-cancerous and osteosarcoma tissues by IHC. (B, C) The expression of SFXN4 and SQOR at RNA and protein levels in normal <t>osteoblast</t> cell and osteosarcoma cell lines through qRT-PCR and western blotting assays. (D, E) Effect of knocking down SFXN4 and SQOR at RNA and protein levels in osteosarcoma cell lines by qRT-PCR and western blotting assays. (F, G) CCK8 and colony formation assays demonstrating the proliferation capacity ability after knocking down SFXN4 and SQOR in osteosarcoma cell lines. ∗ p < 0.05, ∗∗ p < 0.01.
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    Expression and biological functions on growth of SFXN4 and SQOR in osteosarcoma. (A) SFXN4 and SQOR expression in para-cancerous and osteosarcoma tissues by IHC. (B, C) The expression of SFXN4 and SQOR at RNA and protein levels in normal <t>osteoblast</t> cell and osteosarcoma cell lines through qRT-PCR and western blotting assays. (D, E) Effect of knocking down SFXN4 and SQOR at RNA and protein levels in osteosarcoma cell lines by qRT-PCR and western blotting assays. (F, G) CCK8 and colony formation assays demonstrating the proliferation capacity ability after knocking down SFXN4 and SQOR in osteosarcoma cell lines. ∗ p < 0.05, ∗∗ p < 0.01.
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    ATCC human normal osteoblastic cell line
    Expression and biological functions on growth of SFXN4 and SQOR in osteosarcoma. (A) SFXN4 and SQOR expression in para-cancerous and osteosarcoma tissues by IHC. (B, C) The expression of SFXN4 and SQOR at RNA and protein levels in normal <t>osteoblast</t> cell and osteosarcoma cell lines through qRT-PCR and western blotting assays. (D, E) Effect of knocking down SFXN4 and SQOR at RNA and protein levels in osteosarcoma cell lines by qRT-PCR and western blotting assays. (F, G) CCK8 and colony formation assays demonstrating the proliferation capacity ability after knocking down SFXN4 and SQOR in osteosarcoma cell lines. ∗ p < 0.05, ∗∗ p < 0.01.
    Human Normal Osteoblastic Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Cytotoxicity assessment of biomaterials enriched with CAPE derivatives on hFOB 1.19 osteoblasts. ( a ) MTT assay conducted by using 24 h extracts of the biomaterials after 48 h cell culture (PS medium—polystyrene extract served as negative control of cytotoxicity; * statistically significant results compared to PS medium, # statistically significant results compared to mat_control, $ statistically significant results compared to mat_ 1d _L, ^ statistically significant results compared to mat_ 1a _L, p < 0.05, One-way ANOVA followed by Tukey’s test); ( b ) confocal laser scanning microscope images showing live/dead staining of cells cultured on the surface of biomaterials for 48 h (Nomarski contrast was applied to show biomaterial microstructure; viable cells—green fluorescence; dead cells—red fluorescence; magnified 100×, scale bar = 200 µm).

    Journal: Biomedicines

    Article Title: CAPE Derivatives as Potent Agents for Induction of Osteogenic Differentiation in DPSCs and Biomaterial Development

    doi: 10.3390/biomedicines13123039

    Figure Lengend Snippet: Cytotoxicity assessment of biomaterials enriched with CAPE derivatives on hFOB 1.19 osteoblasts. ( a ) MTT assay conducted by using 24 h extracts of the biomaterials after 48 h cell culture (PS medium—polystyrene extract served as negative control of cytotoxicity; * statistically significant results compared to PS medium, # statistically significant results compared to mat_control, $ statistically significant results compared to mat_ 1d _L, ^ statistically significant results compared to mat_ 1a _L, p < 0.05, One-way ANOVA followed by Tukey’s test); ( b ) confocal laser scanning microscope images showing live/dead staining of cells cultured on the surface of biomaterials for 48 h (Nomarski contrast was applied to show biomaterial microstructure; viable cells—green fluorescence; dead cells—red fluorescence; magnified 100×, scale bar = 200 µm).

    Article Snippet: Normal human fetal osteoblast cell line (hFOB 1.19, ATCC CRL-11372) was cultured in a 1:1 mixture of Dulbecco’s Modified Eagle’s Medium and Ham’s F12 Medium, supplemented with 2.5 mM L-glutamine, 0.3 mg/mL G418 (Sigma-Aldrich Chemicals, Warsaw, Poland), and 10% FBS (Pan-Biotech GmbH, Aidenbach, Bavaria, Germany) and maintained at 34 °C (5% CO 2 in air atmosphere).

    Techniques: MTT Assay, Cell Culture, Negative Control, Control, Laser-Scanning Microscopy, Staining, Fluorescence

    Expression and biological functions on growth of SFXN4 and SQOR in osteosarcoma. (A) SFXN4 and SQOR expression in para-cancerous and osteosarcoma tissues by IHC. (B, C) The expression of SFXN4 and SQOR at RNA and protein levels in normal osteoblast cell and osteosarcoma cell lines through qRT-PCR and western blotting assays. (D, E) Effect of knocking down SFXN4 and SQOR at RNA and protein levels in osteosarcoma cell lines by qRT-PCR and western blotting assays. (F, G) CCK8 and colony formation assays demonstrating the proliferation capacity ability after knocking down SFXN4 and SQOR in osteosarcoma cell lines. ∗ p < 0.05, ∗∗ p < 0.01.

    Journal: Frontiers in Immunology

    Article Title: A novel hypoxia- and lactate metabolism-related prognostic signature to characterize the immune landscape and predict immunotherapy response in osteosarcoma

    doi: 10.3389/fimmu.2024.1467052

    Figure Lengend Snippet: Expression and biological functions on growth of SFXN4 and SQOR in osteosarcoma. (A) SFXN4 and SQOR expression in para-cancerous and osteosarcoma tissues by IHC. (B, C) The expression of SFXN4 and SQOR at RNA and protein levels in normal osteoblast cell and osteosarcoma cell lines through qRT-PCR and western blotting assays. (D, E) Effect of knocking down SFXN4 and SQOR at RNA and protein levels in osteosarcoma cell lines by qRT-PCR and western blotting assays. (F, G) CCK8 and colony formation assays demonstrating the proliferation capacity ability after knocking down SFXN4 and SQOR in osteosarcoma cell lines. ∗ p < 0.05, ∗∗ p < 0.01.

    Article Snippet: Human osteosarcoma cell lines (HOS, 143B) and human normal osteoblast cell lines (hFOB1.19) were purchased from Procell Life Science and Technology Co., Ltd. (Wuhan, China).

    Techniques: Expressing, Quantitative RT-PCR, Western Blot