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osteoblast growth medium bulletkit (ogm)  (Lonza)


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    Structured Review

    Lonza osteoblast growth medium bulletkit (ogm)
    Osteoblast Growth Medium Bulletkit (Ogm), supplied by Lonza, 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/ogm+osteoblast+growth+medium+bulletkit/osteoblast+growth+medium+bullet+kit/pm39693871-119-5-10
    Average 90 stars, based on 1 article reviews
    osteoblast growth medium bulletkit (ogm) - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Cell Culture:

    Article Title: Influence of Low Temperature Plasma Oxidizing on the Bioactivity of NiTi Shape Memory Alloy for Medical Applications
    Article Snippet: The cells were grown in an osteoblast basal medium enriched with fetal bovine serum (50 mL/500 mL medium), ascorbic acid (0.5 mL/500 mL medium), GA-1000 (0.5 mL/500 mL medium) antibiotics (OGM Osteoblast Growtth Medium BulletKit, Lonza), in a humid atmosphere of 95% air and 5% CO 2 at 37 °C.



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    Proliferation of <t>osteoblasts</t> cultured on NiTi in the initial state and with a TiO 2 surface layer represented as the number of cells per mm 2 and measured after 24 h, 48 h and 6 days of growth; * p ≤ 0.05 NiTi versus NiTi + TiO 2 .
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    Lonza osteoblast growth medium (ogm bulletkit)
    SCH-induced apoptosis of newly prepared osteosarcoma cell lines and osteosarcoma tumor fragments but not of normal <t>osteoblasts</t> or fibroblasts. A, Osteo7770, Osteo8328, and Osteo8521 cells received SCH at the indicated concentrations for the indicated times. The percentage of apoptotic cells was determined by Annexin V binding. B, fragments of osteosarcoma xenografts grown in mice were cultured in medium containing the indicated concentrations of Rosc, Flav, or SCH for 30 hours. Cell extracts were Western blotted with antibody to PARP or actin. C, density-arrested NHOst, hFOB1.19, and WI-38 cells (gray bars) received the indicated concentrations of SCH for 72 hours. U2OS cells (black bars, positive control) received 20 nmol/L SCH for 72 hours. The percentage of apoptotic cells were determined by Annexin V binding. The 3 panels represent separate experiments. D, cells received the indicated amounts of SCH for 48 or 72 hours. The percentage of apoptotic cells was determined by Annexin V binding.
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    Image Search Results


    Proliferation of osteoblasts cultured on NiTi in the initial state and with a TiO 2 surface layer represented as the number of cells per mm 2 and measured after 24 h, 48 h and 6 days of growth; * p ≤ 0.05 NiTi versus NiTi + TiO 2 .

    Journal: Materials

    Article Title: Influence of Low Temperature Plasma Oxidizing on the Bioactivity of NiTi Shape Memory Alloy for Medical Applications

    doi: 10.3390/ma16186086

    Figure Lengend Snippet: Proliferation of osteoblasts cultured on NiTi in the initial state and with a TiO 2 surface layer represented as the number of cells per mm 2 and measured after 24 h, 48 h and 6 days of growth; * p ≤ 0.05 NiTi versus NiTi + TiO 2 .

    Article Snippet: The cells were grown in an osteoblast basal medium enriched with fetal bovine serum (50 mL/500 mL medium), ascorbic acid (0.5 mL/500 mL medium), GA-1000 (0.5 mL/500 mL medium) antibiotics (OGM Osteoblast Growtth Medium BulletKit, Lonza), in a humid atmosphere of 95% air and 5% CO 2 at 37 °C.

    Techniques: Cell Culture

    Morphology of osteoblasts cultured on the surfaces of NiTi alloy in the initial state ( a , a’ , c , c’ , e , e’ ) and with a TiO 2 surface layer ( b , b’ , d , d’ , f , f’ ) for 24 h ( a , a’ , b , b’ ), 48 h ( c , c’ , d , d’ ) and 6 days ( e , e’ , f , f’ ). SEM images magnified ×60 ( a – f ), ×500 ( a’ – f’ ).

    Journal: Materials

    Article Title: Influence of Low Temperature Plasma Oxidizing on the Bioactivity of NiTi Shape Memory Alloy for Medical Applications

    doi: 10.3390/ma16186086

    Figure Lengend Snippet: Morphology of osteoblasts cultured on the surfaces of NiTi alloy in the initial state ( a , a’ , c , c’ , e , e’ ) and with a TiO 2 surface layer ( b , b’ , d , d’ , f , f’ ) for 24 h ( a , a’ , b , b’ ), 48 h ( c , c’ , d , d’ ) and 6 days ( e , e’ , f , f’ ). SEM images magnified ×60 ( a – f ), ×500 ( a’ – f’ ).

    Article Snippet: The cells were grown in an osteoblast basal medium enriched with fetal bovine serum (50 mL/500 mL medium), ascorbic acid (0.5 mL/500 mL medium), GA-1000 (0.5 mL/500 mL medium) antibiotics (OGM Osteoblast Growtth Medium BulletKit, Lonza), in a humid atmosphere of 95% air and 5% CO 2 at 37 °C.

    Techniques: Cell Culture

    Cell viability of osteoblasts for the 12 HAp samples. The stock solution was diluted in binary dilutions (1/2, 1/4, and 1/8).

    Journal: Materials

    Article Title: Hydroxyapatite from Natural Sources for Medical Applications

    doi: 10.3390/ma15155091

    Figure Lengend Snippet: Cell viability of osteoblasts for the 12 HAp samples. The stock solution was diluted in binary dilutions (1/2, 1/4, and 1/8).

    Article Snippet: The 12 tested samples were placed in a 12-well cell culture plate, with growth medium completely specific to the osteoblast cell line (OGM TM Osteoblast Growth medium BulletKit TM , Lonza, Germany), and incubated for 24 h at 37 °C, in a shaking incubator, 5% CO 2 .

    Techniques:

    Cell proliferation of osteoblasts on HAp samples.

    Journal: Materials

    Article Title: Hydroxyapatite from Natural Sources for Medical Applications

    doi: 10.3390/ma15155091

    Figure Lengend Snippet: Cell proliferation of osteoblasts on HAp samples.

    Article Snippet: The 12 tested samples were placed in a 12-well cell culture plate, with growth medium completely specific to the osteoblast cell line (OGM TM Osteoblast Growth medium BulletKit TM , Lonza, Germany), and incubated for 24 h at 37 °C, in a shaking incubator, 5% CO 2 .

    Techniques:

    SCH-induced apoptosis of newly prepared osteosarcoma cell lines and osteosarcoma tumor fragments but not of normal osteoblasts or fibroblasts. A, Osteo7770, Osteo8328, and Osteo8521 cells received SCH at the indicated concentrations for the indicated times. The percentage of apoptotic cells was determined by Annexin V binding. B, fragments of osteosarcoma xenografts grown in mice were cultured in medium containing the indicated concentrations of Rosc, Flav, or SCH for 30 hours. Cell extracts were Western blotted with antibody to PARP or actin. C, density-arrested NHOst, hFOB1.19, and WI-38 cells (gray bars) received the indicated concentrations of SCH for 72 hours. U2OS cells (black bars, positive control) received 20 nmol/L SCH for 72 hours. The percentage of apoptotic cells were determined by Annexin V binding. The 3 panels represent separate experiments. D, cells received the indicated amounts of SCH for 48 or 72 hours. The percentage of apoptotic cells was determined by Annexin V binding.

    Journal: Molecular cancer therapeutics

    Article Title: The Cyclin-Dependent Kinase Inhibitor SCH 727965 (Dinacliclib) Induces the Apoptosis of Osteosarcoma Cells

    doi: 10.1158/1535-7163.MCT-11-0167

    Figure Lengend Snippet: SCH-induced apoptosis of newly prepared osteosarcoma cell lines and osteosarcoma tumor fragments but not of normal osteoblasts or fibroblasts. A, Osteo7770, Osteo8328, and Osteo8521 cells received SCH at the indicated concentrations for the indicated times. The percentage of apoptotic cells was determined by Annexin V binding. B, fragments of osteosarcoma xenografts grown in mice were cultured in medium containing the indicated concentrations of Rosc, Flav, or SCH for 30 hours. Cell extracts were Western blotted with antibody to PARP or actin. C, density-arrested NHOst, hFOB1.19, and WI-38 cells (gray bars) received the indicated concentrations of SCH for 72 hours. U2OS cells (black bars, positive control) received 20 nmol/L SCH for 72 hours. The percentage of apoptotic cells were determined by Annexin V binding. The 3 panels represent separate experiments. D, cells received the indicated amounts of SCH for 48 or 72 hours. The percentage of apoptotic cells was determined by Annexin V binding.

    Article Snippet: Normal human osteoblasts (NHOst) were purchased from Lonza and were cultured in Osteoblast Growth Medium (OGM BulletKit, Lonza, Catalog # 3207).

    Techniques: Binding Assay, Cell Culture, Western Blot, Positive Control