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msc osteogenic induction medium  (Lonza)


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    Structured Review

    Lonza msc osteogenic induction medium
    Msc Osteogenic Induction Medium, 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/msc+osteogenic+induction+medium/pm31582594-78-8-13?v=Lonza
    Average 90 stars, based on 1 article reviews
    msc osteogenic induction medium - by Bioz Stars, 2026-08
    90/100 stars

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    Osteogenic and <t>adipogenic</t> differentiation of the succeeding passage from bFGF pre‐treated DPSCs. In the Control group, DPSCs (P5) were cultured in bFGF‐free medium and not induced. In the Induction‐CM group, cells (P5) were cultured without bFGF and induced. In the Induction‐prime 20 ng/mL bFGF group, cells (P5) were passaged from bFGF pre‐treated DPSCs and induced. In the Control, cells did not display newly regenerated structure (top panel in A and C). At low and high magnification of induction groups (middle and right column in A and C), mineralized nodules were stained by Alizarin Red and lipid droplets were stained by Oil Red O Scale bar : 200 μm and 100 μm. (B, D) Semi‐quantification of the newly regenerated structure. Induction groups sustained similar potential to differentiate into osteoblast or adipocyte. All data were represented as mean ± SD (n = 3), *** P < .001 vs the Control group
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    Lonza msc osteogenic induction medium
    Osteogenic and <t>adipogenic</t> differentiation of the succeeding passage from bFGF pre‐treated DPSCs. In the Control group, DPSCs (P5) were cultured in bFGF‐free medium and not induced. In the Induction‐CM group, cells (P5) were cultured without bFGF and induced. In the Induction‐prime 20 ng/mL bFGF group, cells (P5) were passaged from bFGF pre‐treated DPSCs and induced. In the Control, cells did not display newly regenerated structure (top panel in A and C). At low and high magnification of induction groups (middle and right column in A and C), mineralized nodules were stained by Alizarin Red and lipid droplets were stained by Oil Red O Scale bar : 200 μm and 100 μm. (B, D) Semi‐quantification of the newly regenerated structure. Induction groups sustained similar potential to differentiate into osteoblast or adipocyte. All data were represented as mean ± SD (n = 3), *** P < .001 vs the Control group
    Msc Osteogenic Induction Medium, 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/msc+osteogenic+induction+medium/pm31582594-78-8-13?v=Lonza
    Average 90 stars, based on 1 article reviews
    msc osteogenic induction medium - by Bioz Stars, 2026-08
    90/100 stars
      Buy from Supplier

    Image Search Results


    Osteogenic and adipogenic differentiation of the succeeding passage from bFGF pre‐treated DPSCs. In the Control group, DPSCs (P5) were cultured in bFGF‐free medium and not induced. In the Induction‐CM group, cells (P5) were cultured without bFGF and induced. In the Induction‐prime 20 ng/mL bFGF group, cells (P5) were passaged from bFGF pre‐treated DPSCs and induced. In the Control, cells did not display newly regenerated structure (top panel in A and C). At low and high magnification of induction groups (middle and right column in A and C), mineralized nodules were stained by Alizarin Red and lipid droplets were stained by Oil Red O Scale bar : 200 μm and 100 μm. (B, D) Semi‐quantification of the newly regenerated structure. Induction groups sustained similar potential to differentiate into osteoblast or adipocyte. All data were represented as mean ± SD (n = 3), *** P < .001 vs the Control group

    Journal: Cell Proliferation

    Article Title: Effects and mechanisms of basic fibroblast growth factor on the proliferation and regenerative profiles of cryopreserved dental pulp stem cells

    doi: 10.1111/cpr.12969

    Figure Lengend Snippet: Osteogenic and adipogenic differentiation of the succeeding passage from bFGF pre‐treated DPSCs. In the Control group, DPSCs (P5) were cultured in bFGF‐free medium and not induced. In the Induction‐CM group, cells (P5) were cultured without bFGF and induced. In the Induction‐prime 20 ng/mL bFGF group, cells (P5) were passaged from bFGF pre‐treated DPSCs and induced. In the Control, cells did not display newly regenerated structure (top panel in A and C). At low and high magnification of induction groups (middle and right column in A and C), mineralized nodules were stained by Alizarin Red and lipid droplets were stained by Oil Red O Scale bar : 200 μm and 100 μm. (B, D) Semi‐quantification of the newly regenerated structure. Induction groups sustained similar potential to differentiate into osteoblast or adipocyte. All data were represented as mean ± SD (n = 3), *** P < .001 vs the Control group

    Article Snippet: In osteogenic and adipogenic differentiation, the OriCellTM MSCs osteogenic and adipogenic induction medium (Cyagen, Santa Clara, USA) were added to 90% confluent DPSCs (P5) according to the manufacturer's instructions.

    Techniques: Control, Cell Culture, Staining