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human osteoblast growth medium  (Cell Applications Inc)


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    Structured Review

    Cell Applications Inc human osteoblast growth medium
    Human Osteoblast Growth Medium, supplied by Cell Applications Inc, used in various techniques. Bioz Stars score: 92/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+osteoblast+growth+medium/Human+Osteoblast+Media/pm37079538-36-43-48
    Average 92 stars, based on 10 article reviews
    human osteoblast growth medium - by Bioz Stars, 2026-10
    92/100 stars

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    Related Articles

    Cell Culture:

    Article Title: Effect of stimulator of interferon genes (STING) signaling on radiation-induced chemokine expression in human osteosarcoma cells.
    Article Snippet: .. Human osteoblasts (hObs) were purchased from, and authenticated by, Cell Applications (#406–05, San Diego, CA, USA), and human OSA cell lines (SAOS-2 (SAOS), SAOS-2-LM6 (LM6), MG63, U2OS) were purchased from the MD Anderson Characterized Cell Line Core (Houston, TX). hObs were cultured in human osteoblast growth medium (#417–500, Cell Applications, San Diego, CA, USA), and OSA cell lines were cultured in complete media consisting of Dulbecco’s Modified Eagles Medium (DMEM, SH30022.01, Cytiva, Logan, UT, USA) supplemented with 10% Fetal Bovine Serum (FBS, 83007–198, VWR) and 1% penicillin/ streptomycin (K952-100ML, VWR, Sanborn, NY, USA). ..

    Article Title: Novel titanium-apatite hybrid scaffolds with spongy bone-like micro architecture intended for spinal application: In vitro and in vivo study.
    Article Snippet: This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive version of record.. This version will undergo additional copyediting, typesetting and review before it is published in its final form, but we are providing this version to give early visibility of the article.. Please note that, during the production process, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

    Article Title: Effect of stimulator of interferon genes (STING) signaling on radiation-induced chemokine expression in human osteosarcoma cells
    Article Snippet: .. Human osteoblasts (hObs) were purchased from, and authenticated by, Cell Applications (#406–05, San Diego, CA, USA), and human OSA cell lines (SAOS-2 (SAOS), SAOS-2-LM6 (LM6), MG63, U2OS) were purchased from the MD Anderson Characterized Cell Line Core (Houston, TX). hObs were cultured in human osteoblast growth medium (#417–500, Cell Applications, San Diego, CA, USA), and OSA cell lines were cultured in complete media consisting of Dulbecco’s Modified Eagles Medium (DMEM, SH30022.01, Cytiva, Logan, UT, USA) supplemented with 10% Fetal Bovine Serum (FBS, 83007–198, VWR) and 1% penicillin/streptomycin (K952-100ML, VWR, Sanborn, NY, USA). ..

    Modification:

    Article Title: Effect of stimulator of interferon genes (STING) signaling on radiation-induced chemokine expression in human osteosarcoma cells.
    Article Snippet: .. Human osteoblasts (hObs) were purchased from, and authenticated by, Cell Applications (#406–05, San Diego, CA, USA), and human OSA cell lines (SAOS-2 (SAOS), SAOS-2-LM6 (LM6), MG63, U2OS) were purchased from the MD Anderson Characterized Cell Line Core (Houston, TX). hObs were cultured in human osteoblast growth medium (#417–500, Cell Applications, San Diego, CA, USA), and OSA cell lines were cultured in complete media consisting of Dulbecco’s Modified Eagles Medium (DMEM, SH30022.01, Cytiva, Logan, UT, USA) supplemented with 10% Fetal Bovine Serum (FBS, 83007–198, VWR) and 1% penicillin/ streptomycin (K952-100ML, VWR, Sanborn, NY, USA). ..

    Article Title: Effect of stimulator of interferon genes (STING) signaling on radiation-induced chemokine expression in human osteosarcoma cells
    Article Snippet: .. Human osteoblasts (hObs) were purchased from, and authenticated by, Cell Applications (#406–05, San Diego, CA, USA), and human OSA cell lines (SAOS-2 (SAOS), SAOS-2-LM6 (LM6), MG63, U2OS) were purchased from the MD Anderson Characterized Cell Line Core (Houston, TX). hObs were cultured in human osteoblast growth medium (#417–500, Cell Applications, San Diego, CA, USA), and OSA cell lines were cultured in complete media consisting of Dulbecco’s Modified Eagles Medium (DMEM, SH30022.01, Cytiva, Logan, UT, USA) supplemented with 10% Fetal Bovine Serum (FBS, 83007–198, VWR) and 1% penicillin/streptomycin (K952-100ML, VWR, Sanborn, NY, USA). ..

    Multiple Displacement Amplification:

    Article Title: SDR enzymes oxidize specific lipidic alkynylcarbinols into cytotoxic protein-reactive species
    Article Snippet: DNA oligonucleotides used in the study are described in the and were ordered from Eurofins Genomics. .. U2OS (ATCC), SAOS-2 (ATCC), 143B (Sigma-Aldrich), HOS (ECACC/Sigma-Aldrich), HS5 (ATCC), G292 clone 141B1 (ECACC/Sigma-Aldrich), HCT-116 (Horizon Discovery), A549 (ATCC), HT-1080 (ATCC), MDA-MB-436 (ATCC), SK-MEL-28 (ATCC), DLD-1 (ATCC), HEK293T (ATCC), MRC5-SV (ECACC/Sigma-Aldrich), HeLa (ATCC) and PC3 (ATCC) cells were grown in DMEM 10% FBS; CAPAN1 (ATCC) in IMDM 20% FBS; T47D (ATCC) and CAPAN2 (ATCC) cells in RPMI1640 10% FBS with Glutamax-I; HAP-1 ( ) (Horizon Discovery) in IMDM 10% FBS and BJ-hTERT (gift from R. Weinberg, Whitehead Institute, Cambridge, USA) in DMEM 15% FBS 16% M199; human adult primary osteoblast (Cell Applications Inc, Sigma-Aldrich) in human osteoblast growth medium (Cell Applications Inc, Sigma-Aldrich). ..

    Article Title: SDR enzymes oxidize specific lipidic alkynylcarbinols into cytotoxic protein-reactive species
    Article Snippet: DNA oligonucleotides used in the study are described in the table below and were ordered from Eurofins Genomics. .. U2OS (ATCC), SAOS-2 (ATCC), 143B (Sigma-Aldrich), HOS (ECACC/Sigma-Aldrich), HS5 (ATCC), G292 clone 141B1 (ECACC/Sigma-Aldrich), HCT-116 (Horizon Discovery), A549 (ATCC), HT-1080 (ATCC), MDA-MB-436 (ATCC), SK-MEL-28 (ATCC), DLD-1 (ATCC), HEK293T (ATCC), MRC5-SV (ECACC/Sigma-Aldrich), HeLa (ATCC) and PC3 (ATCC) cells were grown in DMEM 10% FBS; CAPAN1 (ATCC) in IMDM 20% FBS; T47D (ATCC) and CAPAN2 (ATCC) cells in RPMI1640 10% FBS with Glutamax-I; HAP-1 ( ) (Horizon Discovery) in IMDM 10% FBS and BJ-hTERT (gift from R. Weinberg, Whitehead Institute, Cambridge, USA) in DMEM 15% FBS 16% M199; human adult primary osteoblast (Cell Applications Inc., Sigma-Aldrich) in human osteoblast growth medium (Cell Applications Inc., Sigma-Aldrich). ..



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    Image Search Results


    - Effect of IN44 on metabolic activity and cell viability in periodontal cells. The impact of IN44 (10,50,100 µM) on the metabolic activity and cell viability of epithelial cells, fibroblasts, osteoblasts was measured by AlamarBlue assay ( A ) and Live/Dead assay ( B ) respectively after 24 h of exposure. Live cells in green, dead cells in red (* p < 0.01 compared to control group). One-way ANOVA and Dunnett post hoc

    Journal: BMC Oral Health

    Article Title: The prohibitin ligand IN44 decreases Porphyromonas gingivalis mediated inflammation

    doi: 10.1186/s12903-024-05209-2

    Figure Lengend Snippet: - Effect of IN44 on metabolic activity and cell viability in periodontal cells. The impact of IN44 (10,50,100 µM) on the metabolic activity and cell viability of epithelial cells, fibroblasts, osteoblasts was measured by AlamarBlue assay ( A ) and Live/Dead assay ( B ) respectively after 24 h of exposure. Live cells in green, dead cells in red (* p < 0.01 compared to control group). One-way ANOVA and Dunnett post hoc

    Article Snippet: Primary human osteoblasts (Promocell, Heidelberg, Germany) were cultured in Osteoblast Growth Medium with Osteoblast Growth Medium Supplement Mix (Promocell, Heidelberg, Germany).

    Techniques: Activity Assay, Alamar Blue Assay, Live Dead Assay, Control

    - Effect of IN44 on mitochondrial superoxide production in infected and treated epithelial cells after 45 min and 3 h. Mitochondrial superoxide production in live epithelial cells was detected with MitoSOX by fluorescence microscopy after 45 min–3 h of P. gingivalis infection (Pg) and treatment with IN44 (50 µM) (Pg IN44). Scale bars are 40 μm ( A ). Quantitative fluorescence intensity was analyzed by ECHOPro application ( B ) (* p < 0.05 compared to control, † p < 0.05 compared to infected cells). Scale bars are 170 μm for epithelial cells and 430 μm for fibroblasts and osteoblasts. One-way ANOVA and Dunn post hoc

    Journal: BMC Oral Health

    Article Title: The prohibitin ligand IN44 decreases Porphyromonas gingivalis mediated inflammation

    doi: 10.1186/s12903-024-05209-2

    Figure Lengend Snippet: - Effect of IN44 on mitochondrial superoxide production in infected and treated epithelial cells after 45 min and 3 h. Mitochondrial superoxide production in live epithelial cells was detected with MitoSOX by fluorescence microscopy after 45 min–3 h of P. gingivalis infection (Pg) and treatment with IN44 (50 µM) (Pg IN44). Scale bars are 40 μm ( A ). Quantitative fluorescence intensity was analyzed by ECHOPro application ( B ) (* p < 0.05 compared to control, † p < 0.05 compared to infected cells). Scale bars are 170 μm for epithelial cells and 430 μm for fibroblasts and osteoblasts. One-way ANOVA and Dunn post hoc

    Article Snippet: Primary human osteoblasts (Promocell, Heidelberg, Germany) were cultured in Osteoblast Growth Medium with Osteoblast Growth Medium Supplement Mix (Promocell, Heidelberg, Germany).

    Techniques: Infection, Fluorescence, Microscopy, Control