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tnfrsf11  (Novus Biologicals)


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    Novus Biologicals tnfrsf11
    Tnfrsf11, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 92/100, based on 20 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/tnfrsf11/product/Novus Biologicals
    Average 92 stars, based on 20 article reviews
    tnfrsf11 - by Bioz Stars, 2026-02
    92/100 stars

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    (A) Cells were cultured in an osteogenic medium for 7, 16, or 21 days to <t>RANKL</t> gene. RANKL genes expression was the highest at 16 days post osteoinduction as well as the osteogenic markers Osterix, Runx2, Collagen3A1, Osteopontin and BSP (Fig 6B-6F). Mesenchymal stem cells derived from human adipose tissue (hASCs). Osteoblasts cultured for 7 days with osteoinduction medium (Ost. 7 days). Osteoblasts cultured for 16 days with osteoinduction medium (Ost. 16 days). Osteoblasts cultured for 21 days with osteoinduction medium (Ost. 21 days). An ANOVA followed by Tukey's test was used to analyze the data. P <0.005.
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    (A) Cells were cultured in an osteogenic medium for 7, 16, or 21 days to RANKL gene. RANKL genes expression was the highest at 16 days post osteoinduction as well as the osteogenic markers Osterix, Runx2, Collagen3A1, Osteopontin and BSP (Fig 6B-6F). Mesenchymal stem cells derived from human adipose tissue (hASCs). Osteoblasts cultured for 7 days with osteoinduction medium (Ost. 7 days). Osteoblasts cultured for 16 days with osteoinduction medium (Ost. 16 days). Osteoblasts cultured for 21 days with osteoinduction medium (Ost. 21 days). An ANOVA followed by Tukey's test was used to analyze the data. P <0.005.

    Journal: PLoS ONE

    Article Title: Cell viability assessed in a reproducible model of human osteoblasts derived from human adipose-derived stem cells

    doi: 10.1371/journal.pone.0194847

    Figure Lengend Snippet: (A) Cells were cultured in an osteogenic medium for 7, 16, or 21 days to RANKL gene. RANKL genes expression was the highest at 16 days post osteoinduction as well as the osteogenic markers Osterix, Runx2, Collagen3A1, Osteopontin and BSP (Fig 6B-6F). Mesenchymal stem cells derived from human adipose tissue (hASCs). Osteoblasts cultured for 7 days with osteoinduction medium (Ost. 7 days). Osteoblasts cultured for 16 days with osteoinduction medium (Ost. 16 days). Osteoblasts cultured for 21 days with osteoinduction medium (Ost. 21 days). An ANOVA followed by Tukey's test was used to analyze the data. P <0.005.

    Article Snippet: The expression levels of RANKL (Applied Biosystems TNFRSF11-Hs00243522_m1 assay), was performed using the TaqMan commercial qPCR kit (Invitrogen) according to the manufacturer's instructions.

    Techniques: Cell Culture, Expressing, Derivative Assay

    (A) CD45RO. (B) CD105. (C) STRO-1. (D) The arrows indicate the perinuclear location of Nanog. (E) The arrows indicate the location of RANKL. (F) Levels of expression of markers. Cell images showing the expression of the markers CD 45RO, RANKL, Nanog, CD105, and STRO-1 in osteoblasts cultured in osteogenic medium for 16 days. Data are expressed as mean ± standard deviation. An ANOVA followed by Tukey’s test was used to analyze the data. P < 0.005.

    Journal: PLoS ONE

    Article Title: Cell viability assessed in a reproducible model of human osteoblasts derived from human adipose-derived stem cells

    doi: 10.1371/journal.pone.0194847

    Figure Lengend Snippet: (A) CD45RO. (B) CD105. (C) STRO-1. (D) The arrows indicate the perinuclear location of Nanog. (E) The arrows indicate the location of RANKL. (F) Levels of expression of markers. Cell images showing the expression of the markers CD 45RO, RANKL, Nanog, CD105, and STRO-1 in osteoblasts cultured in osteogenic medium for 16 days. Data are expressed as mean ± standard deviation. An ANOVA followed by Tukey’s test was used to analyze the data. P < 0.005.

    Article Snippet: The expression levels of RANKL (Applied Biosystems TNFRSF11-Hs00243522_m1 assay), was performed using the TaqMan commercial qPCR kit (Invitrogen) according to the manufacturer's instructions.

    Techniques: Expressing, Cell Culture, Standard Deviation