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normal human osteoblast (nhost) cells (clonetics® , cambrex)  (Cambrex)

 
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    Cambrex normal human osteoblast (nhost) cells (clonetics® , cambrex)
    Normal Human Osteoblast (Nhost) Cells (Clonetics® , Cambrex), supplied by Cambrex, 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/product/normal+human+osteoblasts+clonetics/osteoblasts/pm18606205-45-0-7
    Average 90 stars, based on 1 article reviews
    normal human osteoblast (nhost) cells (clonetics® , cambrex) - by Bioz Stars, 2026-09
    90/100 stars

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    other:

    Article Title: Dominant Negative LRP5 Decreases Tumorigenicity and Metastasis of Osteosarcoma in an Animal Model
    Article Snippet: Normal human osteoblasts (NHOst) were obtained from the Clonetics® collection (Cambrex Corp, East Rutherford, NJ) and maintained in the OGM-Osteoblast Growth Medium (Cambrex Corp).



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    Image Search Results


    ADSC-EV uptake by osteoblasts. The hFOBs ( A ) and hOBs ( B ) were treated with CM-DiI-labeled ADSC-EVs at concentrations of 0 (Control: control group) or 1 × 10 9 particles/mL (EVs: EV group) for 5 days, and images at days 1 and 5 were obtained using a camera under confocal microscopy. Cell nucleus, blue fluorescence stain; cytoplasm, green fluorescence stain; and CM-DiI-labeled ADSC-EVs, red fluorescence stain.

    Journal: Biomedicines

    Article Title: Enhancement of Osteoblast Function through Extracellular Vesicles Derived from Adipose-Derived Stem Cells

    doi: 10.3390/biomedicines10071752

    Figure Lengend Snippet: ADSC-EV uptake by osteoblasts. The hFOBs ( A ) and hOBs ( B ) were treated with CM-DiI-labeled ADSC-EVs at concentrations of 0 (Control: control group) or 1 × 10 9 particles/mL (EVs: EV group) for 5 days, and images at days 1 and 5 were obtained using a camera under confocal microscopy. Cell nucleus, blue fluorescence stain; cytoplasm, green fluorescence stain; and CM-DiI-labeled ADSC-EVs, red fluorescence stain.

    Article Snippet: The human nontumor osteoblast (hFOB) cell line (hFOB 1.19, ATCC CRL-1137, Manassas, VA, USA) [ ] and primary normal human osteoblasts (hOBs; Clonetic; Lonza, Basel, Switzerland) were used in the present study.

    Techniques: Labeling, Control, Confocal Microscopy, Fluorescence, Staining

    Effect of ADSC-EVs on the survival of osteoblasts. The hFOBs ( A ) and hOBs ( B ) were treated with ADSC-EVs at concentrations of 0 (Control: control group) or 10 9 particles/mL (EVs: EV group) for 5 days and analyzed for survival. Live/dead cell assays were performed for hFOBs and hOBs to determine the cell survival on days 1 and 5. Green fluorescence indicates live cells (Live), whereas red fluorescence indicates dead cells (Dead). The hFOBs and hOBs remained alive on days 1 and 5 after the ADSC-EV treatment.

    Journal: Biomedicines

    Article Title: Enhancement of Osteoblast Function through Extracellular Vesicles Derived from Adipose-Derived Stem Cells

    doi: 10.3390/biomedicines10071752

    Figure Lengend Snippet: Effect of ADSC-EVs on the survival of osteoblasts. The hFOBs ( A ) and hOBs ( B ) were treated with ADSC-EVs at concentrations of 0 (Control: control group) or 10 9 particles/mL (EVs: EV group) for 5 days and analyzed for survival. Live/dead cell assays were performed for hFOBs and hOBs to determine the cell survival on days 1 and 5. Green fluorescence indicates live cells (Live), whereas red fluorescence indicates dead cells (Dead). The hFOBs and hOBs remained alive on days 1 and 5 after the ADSC-EV treatment.

    Article Snippet: The human nontumor osteoblast (hFOB) cell line (hFOB 1.19, ATCC CRL-1137, Manassas, VA, USA) [ ] and primary normal human osteoblasts (hOBs; Clonetic; Lonza, Basel, Switzerland) were used in the present study.

    Techniques: Control, Fluorescence

    Effect of ADSC-EVs on the proliferation of osteoblasts. The hFOBs ( A ) and hOBs ( B ) were treated with ADSC-EVs at concentrations of 0 (Control: control group) or 1 × 10 7 –1 × 10 9 particles/mL (EVs: EV group) for 5 days and analyzed for cell proliferation. MTS assays were performed for hFOBs and hOBs on day 5 to determine the cell proliferation. Cell proliferation of hFOBs and hOBs was enhanced after the ADSC-EV treatment. Data are presented as the mean ± SD ( n = 6). * p < 0.05 and ** p < 0.01 for comparisons with the control group. # p < 0.05 and ## p < 0.01 for comparisons between the two groups.

    Journal: Biomedicines

    Article Title: Enhancement of Osteoblast Function through Extracellular Vesicles Derived from Adipose-Derived Stem Cells

    doi: 10.3390/biomedicines10071752

    Figure Lengend Snippet: Effect of ADSC-EVs on the proliferation of osteoblasts. The hFOBs ( A ) and hOBs ( B ) were treated with ADSC-EVs at concentrations of 0 (Control: control group) or 1 × 10 7 –1 × 10 9 particles/mL (EVs: EV group) for 5 days and analyzed for cell proliferation. MTS assays were performed for hFOBs and hOBs on day 5 to determine the cell proliferation. Cell proliferation of hFOBs and hOBs was enhanced after the ADSC-EV treatment. Data are presented as the mean ± SD ( n = 6). * p < 0.05 and ** p < 0.01 for comparisons with the control group. # p < 0.05 and ## p < 0.01 for comparisons between the two groups.

    Article Snippet: The human nontumor osteoblast (hFOB) cell line (hFOB 1.19, ATCC CRL-1137, Manassas, VA, USA) [ ] and primary normal human osteoblasts (hOBs; Clonetic; Lonza, Basel, Switzerland) were used in the present study.

    Techniques: Control

    ADSC-EVs promoted osteogenic marker gene expression in osteoblasts. The hFOBs ( A ) and hOBs ( B ) were treated with ADSC-EVs at concentrations of 0 (Control: control group) or 10 9 particles/mL (EVs: EV group) for 5 days. The mRNA expression levels of the osteogenic marker genes (runt-related transcription factor 2 ( Runx2 ), osteocalcin ( OC ), collagen type I ( Col-I ), and alkaline phosphatase ( ALP )) of hFOBs and hOBs were measured. Gene expression levels are expressed relative to the control group, which is defined as 1. Data are presented as the mean ± SD ( n = 3). * p < 0.05 and ** p < 0.01 for comparisons with the control group.

    Journal: Biomedicines

    Article Title: Enhancement of Osteoblast Function through Extracellular Vesicles Derived from Adipose-Derived Stem Cells

    doi: 10.3390/biomedicines10071752

    Figure Lengend Snippet: ADSC-EVs promoted osteogenic marker gene expression in osteoblasts. The hFOBs ( A ) and hOBs ( B ) were treated with ADSC-EVs at concentrations of 0 (Control: control group) or 10 9 particles/mL (EVs: EV group) for 5 days. The mRNA expression levels of the osteogenic marker genes (runt-related transcription factor 2 ( Runx2 ), osteocalcin ( OC ), collagen type I ( Col-I ), and alkaline phosphatase ( ALP )) of hFOBs and hOBs were measured. Gene expression levels are expressed relative to the control group, which is defined as 1. Data are presented as the mean ± SD ( n = 3). * p < 0.05 and ** p < 0.01 for comparisons with the control group.

    Article Snippet: The human nontumor osteoblast (hFOB) cell line (hFOB 1.19, ATCC CRL-1137, Manassas, VA, USA) [ ] and primary normal human osteoblasts (hOBs; Clonetic; Lonza, Basel, Switzerland) were used in the present study.

    Techniques: Marker, Gene Expression, Control, Expressing

    ADSC-EVs promote ALP activity, calcium deposition, and collagen type I ( Col-I ) synthesis in osteoblasts. The hFOBs ( A ) and hOBs ( B ) were treated with ADSC-EVs at concentrations of 0 (Control: control group) or 1 × 10 9 particles/mL (EVs: EV group) for 12 days and analyzed through von Kossa staining, Alizarin red S staining and quantification, and ELISA for ALP activity and Col-I synthesis. Data are presented as the mean ± SD ( n = 3). * p < 0.05 and ** p < 0.01 for comparisons with the control group.

    Journal: Biomedicines

    Article Title: Enhancement of Osteoblast Function through Extracellular Vesicles Derived from Adipose-Derived Stem Cells

    doi: 10.3390/biomedicines10071752

    Figure Lengend Snippet: ADSC-EVs promote ALP activity, calcium deposition, and collagen type I ( Col-I ) synthesis in osteoblasts. The hFOBs ( A ) and hOBs ( B ) were treated with ADSC-EVs at concentrations of 0 (Control: control group) or 1 × 10 9 particles/mL (EVs: EV group) for 12 days and analyzed through von Kossa staining, Alizarin red S staining and quantification, and ELISA for ALP activity and Col-I synthesis. Data are presented as the mean ± SD ( n = 3). * p < 0.05 and ** p < 0.01 for comparisons with the control group.

    Article Snippet: The human nontumor osteoblast (hFOB) cell line (hFOB 1.19, ATCC CRL-1137, Manassas, VA, USA) [ ] and primary normal human osteoblasts (hOBs; Clonetic; Lonza, Basel, Switzerland) were used in the present study.

    Techniques: Activity Assay, Control, Staining, Enzyme-linked Immunosorbent Assay