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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+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, 2026-09
    90/100 stars

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    Related Articles

    Cell Culture:

    Article Title: Exploring the heterogeneity of osteosarcoma cell characteristics and metabolic states and their association with clinical prognosis
    Article Snippet: .. NHOST was cultured in OGM BulletKit (Lonza, Switzerland) medium; MG63 was maintained in Minimum Essential Medium (MEM, Hyclone, USA); SAOS2 and U2OS were cultured using McCoy’s 5A medium (Hyclone, USA); and HOS was grown in Dulbecco’s Modified Eagle Medium (DMEM, Hyclone, USA). .. All culture media were supplemented with 10% fetal bovine serum (FBS, Hyclone, USA), and 1% penicillin-streptomycin mixed solution (Keygen, China) was added to inhibit bacterial growth.

    Article Title: Poly(ε-caprolactone)-based membranes with tunable physicochemical, bioactive and osteoinductive properties
    Article Snippet: Material sterilization For the cell culture, membranes (round samples matching the size of wells of 48-well culture plate) were sterilized by soaking in 70% ethanol for 30 min, further both sides of samples were sterilized with UV-C light for 30 min each and washed with sterile phosphate-buffered saline (PBS, HyClone, USA). .. Cell culture The normal human osteoblasts (NHOst, Lonza, USA) were expanded in 75 cm2 tissue culture flasks (NuncTM, Denmark) in complete osteoblast growth medium OGM BulletKit (Lonza, USA) containing 10% FBS, 0.1% ascorbic acid and 0.1% GA1000 (gentamicin sulphate and amphotericin-B) at 37 °C in a humidified, 5% CO2 atmosphere. ..

    Modification:

    Article Title: Exploring the heterogeneity of osteosarcoma cell characteristics and metabolic states and their association with clinical prognosis
    Article Snippet: .. NHOST was cultured in OGM BulletKit (Lonza, Switzerland) medium; MG63 was maintained in Minimum Essential Medium (MEM, Hyclone, USA); SAOS2 and U2OS were cultured using McCoy’s 5A medium (Hyclone, USA); and HOS was grown in Dulbecco’s Modified Eagle Medium (DMEM, Hyclone, USA). .. All culture media were supplemented with 10% fetal bovine serum (FBS, Hyclone, USA), and 1% penicillin-streptomycin mixed solution (Keygen, China) was added to inhibit bacterial growth.

    other:

    Article Title: Conductive PANI patterns on electrospun PCL/gelatin scaffolds modified with bioactive particles for bone tissue engineering
    Article Snippet: In this article a method of inkjet printing applied to create conductive patterns on electrospun composite scaffolds for bone tissue engineering is presented.. By incorporation of conductive polyaniline and bioactive particles and drugs (osteogenon, calcium phosphate nanoparticles) within an electrospun polycaprolactone/gelatin composite scaffold, we have obtained a biocompatible, bioactive, hybrid scaffold system, which provides an electrically conductive environment.. & 2014 Published by Elsevier B.V.

    Article Title: Laser-treated electrospun fibers loaded with nano-hydroxyapatite for bone tissue engineering.
    Article Snippet: Normal human osteoblasts (NHOst, Lonza, Belgium) were grown in OGM culture medium, supplemented with 10 % FBS, ascorbic acid and 5 % solution of gentamicin and amphotericin-B (OGM BulletKit, Lonza, USA) as the manufacturer indicates in an atmosphere containing 5 % CO2 at 37oC.

    Article Title: Electrospun polymer scaffolds modified with drugs for tissue engineering.
    Article Snippet: The purpose of this paper was to fabricate nanofibrous scaffolds containing osseinhydroxyapatite complex (osteogenon) to mimic the native bone extracellular matrix.. Polylactide (PLDL) and polycaprolactone (PCL) were used to prepare scaffolds using electrospinning.. Unfortunately, both of these biodegradable polymers have poor cell recognition sites leading to poor cell affinity and adhesion, therefore, based on our previous experience, osteogenon-drug was used at the stage of fibres forming by electrospinning.

    Article Title: Multifunctional polymer coatings for titanium implants.
    Article Snippet: The aim of this work was to modify the surface of the titanium implants by application of multifunctional polymer coatings based on polyurethane and its composites with graphene and β-TCP.. Graphene was used as an antibacterial agent, TCP as a bioactive component, and polymer coating as a corrosion protection of metal.. As a result, materials with different surface characteristic, from hydrophilic to hydrophobic, varying in bioactivity and biocompatibility, were obtained.



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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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    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: