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normal human osteoblast line hfob1 19  (ATCC)


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    Structured Review

    ATCC normal human osteoblast line hfob1 19
    Normal Human Osteoblast Line Hfob1 19, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 836 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/normal+osteoblasts/hFOB+1%2E19/10__1007_slash_s13402___026___01277___4-79-14-23
    Average 98 stars, based on 836 article reviews
    normal human osteoblast line hfob1 19 - by Bioz Stars, 2026-10
    98/100 stars

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    Related Articles

    other:

    Article Title: Deciphering the oncogenic network: how C1QTNF1-AS1 modulates osteosarcoma through miR-34a-5p and glycolytic pathways.
    Article Snippet: Human osteosarcoma cell lines (including MG63, Saos-2, U2OS and HOS) and normal osteoblasts (HFOB1.19) were obtained from the ATCC Cell Bank located in Manassas, Virginia, USA.

    Article Title: MAT2A inhibits the ferroptosis in osteosarcoma progression regulated by miR-26b-5p
    Article Snippet: Normal osteoblasts (hFOB 1.19) and OS cell lines (MNNG/HOS and U2OS) were purchased from American Type Culture Collection (ATCC) (Manassas, VA, USA).

    Article Title: Long non-coding RNA PCAT6 promotes the development of osteosarcoma by increasing MDM2 expression
    Article Snippet: Normal osteoblasts (hFOB1.19) and human osteosarcoma cell lines (Saos2, MG63, U2OS and HOS) used in the present study were purchased from American Type Culture Collection.

    Article Title: MAT2A inhibits the ferroptosis in osteosarcoma progression regulated by miR-26b-5p.
    Article Snippet: Normal osteoblasts (hFOB 1.19) and OS cell lines (MNNG/HOS and U2OS) were purchased from American Type Culture Collection (ATCC) (Manassas, VA, USA).

    Article Title: Deciphering the oncogenic network: how C1QTNF1-AS1 modulates osteosarcoma through miR-34a-5p and glycolytic pathways
    Article Snippet: Human osteosarcoma cell lines (including MG63, Saos-2, U2OS and HOS) and normal osteoblasts (HFOB1.19) were obtained from the ATCC Cell Bank located in Manassas, Virginia, USA.

    Modification:

    Article Title: miR-451a Inhibits the Growth and Invasion of Osteosarcoma via Targeting TRIM66.
    Article Snippet: .. Osteosarcoma cell lines (Saos-2, U2OS, and MG63) and normal osteoblasts (hFOB 1.19) purchased at American Type Culture Collection (Manassas, Virginia) were maintained in Dulbecco modified Eagle medium (DMEM; Invitrogen, Thermo Fisher Scientific, Inc, Waltham, Massachusetts) with 10% fetal bovine serum (FBS, Invitrogen) in a 37 C humidified incubator containing 5% CO2 and 95% air. .. MicroRNA-451a mimic (50-AAACCGUUACCAUUACUGAGUU-30) and negative control (negative control miRNA for mimic [NC] mimic; 50-AUCUGAACGGAUCCUUAUUAAC-30) were purchased at GenePharma (Shanghai, China).

    Cell Culture:

    Article Title: C1QTNF1-AS1/miR-346 axis suppresses osteosarcoma progression via dual inhibition of LDHA/PDK1-mediated Warburg effect.
    Article Snippet: .. Human OS cell lines (MG63, Saos-2, U2OS, HOS) and normal osteoblasts (HFOB1.19) from ATCC were cultured in Eagle’s medium with 10% FBS and 0.1% penicillin-streptomycin. ..

    Article Title: C1QTNF1-AS1/miR-346 axis suppresses osteosarcoma progression via dual inhibition of LDHA/PDK1-mediated Warburg effect
    Article Snippet: .. Human OS cell lines (MG63, Saos-2, U2OS, HOS) and normal osteoblasts (HFOB1.19) from ATCC were cultured in Eagle’s medium with 10% FBS and 0.1% penicillin-streptomycin. ..



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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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    ATCC normal osteoblasts
    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 Osteoblasts, 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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    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