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culture primary human fetal osteoblast cells  (ATCC)


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    ATCC culture primary human fetal osteoblast cells
    Culture Primary Human Fetal Osteoblast Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 2806 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/culture+mouse+osteoblastic+cells/TIBx%3B+Epithelial+liver%3B+Mouse/pmc12383066-64-16-24
    Average 97 stars, based on 2806 article reviews
    culture primary human fetal osteoblast cells - by Bioz Stars, 2026-11
    97/100 stars

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    Cell Culture:

    Article Title: Osteogenesis-Related Gene Expression and Guided Bone Regeneration of a Strontium-Doped Calcium-Phosphate-Coated Titanium Mesh.
    Article Snippet: Subscriber access provided by BUPMC - Bibliothèque Universitaire Pierre et Marie Curie is published by the American Chemical Society.. 1155 Sixteenth Street N.W., Washington, DC 20036 Published by American Chemical Society.. Copyright © American Chemical Society.

    Modification:

    Article Title: Osteogenesis-Related Gene Expression and Guided Bone Regeneration of a Strontium-Doped Calcium-Phosphate-Coated Titanium Mesh.
    Article Snippet: Subscriber access provided by BUPMC - Bibliothèque Universitaire Pierre et Marie Curie is published by the American Chemical Society.. 1155 Sixteenth Street N.W., Washington, DC 20036 Published by American Chemical Society.. Copyright © American Chemical Society.



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    Comparison of growth, metabolic, proliferative parameters of <t> MC3T3-E1 </t> cells when treated with mitogenic doses of crude ethanolic extract of CQ (CQ-E), Ethyl acetate fraction (CQ-EA) and n-Butanol fraction of CQ (CQ-B). The control cell were treated with 0.05% DMSO supplemented complete growth medium. CQ treated cells had compete growth medium supplemented with respective concentrations of respective CQ extract/ fractions. The positive and negative sign indicate the percentage increase or decrease in the tested parameters in response to CQ treatment.
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    Image Search Results


    Osteoblast cell viability determination for ( a ) TiAlV substrate, 3D-printed coating on TiAlV substrate (no drug), and CLIN-loaded 3D-printed coating on TiAlV substrate (CLIN) and ( b ) AISI 316LVM substrate, 3D-printed coating on AISI 316LVM substrate (no drug), and CLIN-loaded 3D-printed coating on AISI 316LVM substrate (CLIN) using the MTT (3(4,5 dimethylthiazolyl-2)-2,5-diphenyltetrazolium) assay and the control (cell growth in the advanced DMEM and FBS medium indicated by red line). Error bars represent standard deviation.

    Journal: Materials

    Article Title: Clindamycin-Based 3D-Printed and Electrospun Coatings for Treatment of Implant-Related Infections

    doi: 10.3390/ma14061464

    Figure Lengend Snippet: Osteoblast cell viability determination for ( a ) TiAlV substrate, 3D-printed coating on TiAlV substrate (no drug), and CLIN-loaded 3D-printed coating on TiAlV substrate (CLIN) and ( b ) AISI 316LVM substrate, 3D-printed coating on AISI 316LVM substrate (no drug), and CLIN-loaded 3D-printed coating on AISI 316LVM substrate (CLIN) using the MTT (3(4,5 dimethylthiazolyl-2)-2,5-diphenyltetrazolium) assay and the control (cell growth in the advanced DMEM and FBS medium indicated by red line). Error bars represent standard deviation.

    Article Snippet: To test the biocompatibility of materials (ES and 3D-printed coatings on AISI 316LVM and TiAlV substrates), an MTT test on osteoblast cell culture (hFOB 1.19, ATCC CRL-11372) was performed.

    Techniques: Control, Standard Deviation

    Comparison of growth, metabolic, proliferative parameters of  MC3T3-E1  cells when treated with mitogenic doses of crude ethanolic extract of CQ (CQ-E), Ethyl acetate fraction (CQ-EA) and n-Butanol fraction of CQ (CQ-B). The control cell were treated with 0.05% DMSO supplemented complete growth medium. CQ treated cells had compete growth medium supplemented with respective concentrations of respective CQ extract/ fractions. The positive and negative sign indicate the percentage increase or decrease in the tested parameters in response to CQ treatment.

    Journal: Journal of cellular physiology

    Article Title: Ethyl Acetate and n-Butanol Fraction of Cissus quadrangularis Promotes the Mineralization Potential of Murine Pre-Osteoblast Cell Line MC3T3-E1 (Sub-clone 4)

    doi: 10.1002/jcp.27707

    Figure Lengend Snippet: Comparison of growth, metabolic, proliferative parameters of MC3T3-E1 cells when treated with mitogenic doses of crude ethanolic extract of CQ (CQ-E), Ethyl acetate fraction (CQ-EA) and n-Butanol fraction of CQ (CQ-B). The control cell were treated with 0.05% DMSO supplemented complete growth medium. CQ treated cells had compete growth medium supplemented with respective concentrations of respective CQ extract/ fractions. The positive and negative sign indicate the percentage increase or decrease in the tested parameters in response to CQ treatment.

    Article Snippet: Cell culture Mouse pre-osteoblast cell line MC3T3-E1 (sub-clone 4) (ATCC – 2593TM) was purchased from American Type Culture Collection.

    Techniques: Comparison, Control, Activity Assay, BrdU Incorporation Assay

    Comparison of outset of mineralization process in  MC3T3-E1  cells and the amount of mineral deposited determined by alizarin red s semi-quantification method after treatment with mitogenic doses of crude ethanolic extract of CQ (CQ-E), Ethyl acetate fraction (CQ-EA) and n-Butanol fraction of CQ (CQ-B). The positive and negative sign indicate percentage increase or decrease in mineral deposition compared to positive control (PC). Positive control cells were treated with osteogenic induction medium only. CQ-E, CQ-EA and CQ-B treated cultures had osteogenic induction medium supplemented with respective concentrations of the CQ.

    Journal: Journal of cellular physiology

    Article Title: Ethyl Acetate and n-Butanol Fraction of Cissus quadrangularis Promotes the Mineralization Potential of Murine Pre-Osteoblast Cell Line MC3T3-E1 (Sub-clone 4)

    doi: 10.1002/jcp.27707

    Figure Lengend Snippet: Comparison of outset of mineralization process in MC3T3-E1 cells and the amount of mineral deposited determined by alizarin red s semi-quantification method after treatment with mitogenic doses of crude ethanolic extract of CQ (CQ-E), Ethyl acetate fraction (CQ-EA) and n-Butanol fraction of CQ (CQ-B). The positive and negative sign indicate percentage increase or decrease in mineral deposition compared to positive control (PC). Positive control cells were treated with osteogenic induction medium only. CQ-E, CQ-EA and CQ-B treated cultures had osteogenic induction medium supplemented with respective concentrations of the CQ.

    Article Snippet: Cell culture Mouse pre-osteoblast cell line MC3T3-E1 (sub-clone 4) (ATCC – 2593TM) was purchased from American Type Culture Collection.

    Techniques: Comparison, Positive Control