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anti runx2 rabbit polyclonal  (Novus Biologicals)


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    Novus Biologicals anti runx2 rabbit polyclonal
    Anti Runx2 Rabbit Polyclonal, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 92/100, based on 15 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/nbp1+77461/RUNX2%2FCBFA1+Antibody+-+BSA+Free/pmc12221681-285-47-51
    Average 92 stars, based on 15 article reviews
    anti runx2 rabbit polyclonal - by Bioz Stars, 2026-09
    92/100 stars

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    Novus Biologicals 213805 polyclonal sost antibody
    Fig. 5. Osteocyte morphology and functionality in mineralized and non-mineralized microgels. A-B and E-F represent the confocal images of non-mineralized (A-B) and mineralized (E-F) samples. Microgels stained with actin (green), DAPI (blue), and <t>SOST</t> (red) and SOST intensity (normalized fluorescence per cell) in mineralized microgels (A-H, K-L). Also, the dendrite length in μm (I) and the number of dendrites per cell (I-J) were not significantly different between mineralized and non-mineralized samples. Statistical differences are represented by **** p < 0.0001 after the One-way ANOVA test post-Turkey’s corrections.
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    Osteocyte morphology and functionality in mineralized and non-mineralized microgels. A-B and E-F represent the confocal images of non-mineralized (A-B) and mineralized (E-F) samples. Microgels stained with actin, DAPI, and <t>SOST</t> revels higher cell number and SOST intensity (normalized fluorescence per cell) in mineralized microgels (A-H, K-L). Also, the dendrite length in μm (I) and the number of dendrites per cell (I-J) were not significantly different between mineralized and non-mineralized samples. Statistical differences are represented by **** p<0.0001 after the One-way ANOVA test post-Turkey’s corrections.
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    Novus Biologicals runx2
    Fig. 6. Repopulation of adseverin-positive chondrocytes attenuated changes in Indian hedgehog and <t>Runx2</t> expression despite increased proliferation, ap- optosis, collagen type X, and decreased aggrecan and F-actin. Immunohistochemical staining and quantification at 18 weeks of (A and B) adseverin, (C and D) Ihh, and (E and F) Ki67, as well as immunostaining for (G) aggrecan in the articular cartilage of Adseverin−/−and Adseverin+/+ mice. Scale bars, 200 μm. (H) Apoptotic chon- drocytes and the actin cytoskeleton were detected by immunofluorescent staining with TUNEL (green) and phalloidin (red), respectively. DAPI (blue) stains nuclei. Scale bar, 400 μm. Higher-magnification images of the red or white dashed box in regions are in fig. S6. (I) Quantification of TUNEL-positive cells in the articular cartilage of Adseverin−/−and Adseverin+/+ mice. Immunohistochemical staining of hypertrophic markers (J) Runx2 with (K) quantification and (L) collagen type X in the articular cartilage of Adseverin−/−versus Adseverin+/+ mice. Dot plots represent the mean with minimum and maximum values. Statistical analysis was assessed using Student’s unpaired two-tailed t test (B, D, F, I, and K). The number of biological replicates in each group and P values are indicated in the figure.
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    Image Search Results


    Fig. 5. Osteocyte morphology and functionality in mineralized and non-mineralized microgels. A-B and E-F represent the confocal images of non-mineralized (A-B) and mineralized (E-F) samples. Microgels stained with actin (green), DAPI (blue), and SOST (red) and SOST intensity (normalized fluorescence per cell) in mineralized microgels (A-H, K-L). Also, the dendrite length in μm (I) and the number of dendrites per cell (I-J) were not significantly different between mineralized and non-mineralized samples. Statistical differences are represented by **** p < 0.0001 after the One-way ANOVA test post-Turkey’s corrections.

    Journal: Biomaterials advances

    Article Title: In vitro development and optimization of cell-laden injectable bioprinted gelatin methacryloyl (GelMA) microgels mineralized on the nanoscale.

    doi: 10.1016/j.bioadv.2024.213805

    Figure Lengend Snippet: Fig. 5. Osteocyte morphology and functionality in mineralized and non-mineralized microgels. A-B and E-F represent the confocal images of non-mineralized (A-B) and mineralized (E-F) samples. Microgels stained with actin (green), DAPI (blue), and SOST (red) and SOST intensity (normalized fluorescence per cell) in mineralized microgels (A-H, K-L). Also, the dendrite length in μm (I) and the number of dendrites per cell (I-J) were not significantly different between mineralized and non-mineralized samples. Statistical differences are represented by **** p < 0.0001 after the One-way ANOVA test post-Turkey’s corrections.

    Article Snippet: Cells were permeabilized with 0.1 % Triton X100, blocked with 1.5 % bovine serum albumin in PBS, and incubated at room temperature for 1 h. Samples were then washed in PBS and incubated with the primary antibody (rabbit M.G. da Costa Sousa et al. Biomaterials Advances 159 (2024) 213805 polyclonal SOST antibody (Novus Biologicals, NBP1-77461)) (1:100 dilution), overnight at 4 ◦C.

    Techniques: Staining, Fluorescence

    Osteocyte morphology and functionality in mineralized and non-mineralized microgels. A-B and E-F represent the confocal images of non-mineralized (A-B) and mineralized (E-F) samples. Microgels stained with actin, DAPI, and SOST revels higher cell number and SOST intensity (normalized fluorescence per cell) in mineralized microgels (A-H, K-L). Also, the dendrite length in μm (I) and the number of dendrites per cell (I-J) were not significantly different between mineralized and non-mineralized samples. Statistical differences are represented by **** p<0.0001 after the One-way ANOVA test post-Turkey’s corrections.

    Journal: bioRxiv

    Article Title: In vitro development and optimization of cell-laden injectable bioprinted gelatin methacryloyl (GelMA) microgels mineralized on the nanoscale

    doi: 10.1101/2023.10.10.560919

    Figure Lengend Snippet: Osteocyte morphology and functionality in mineralized and non-mineralized microgels. A-B and E-F represent the confocal images of non-mineralized (A-B) and mineralized (E-F) samples. Microgels stained with actin, DAPI, and SOST revels higher cell number and SOST intensity (normalized fluorescence per cell) in mineralized microgels (A-H, K-L). Also, the dendrite length in μm (I) and the number of dendrites per cell (I-J) were not significantly different between mineralized and non-mineralized samples. Statistical differences are represented by **** p<0.0001 after the One-way ANOVA test post-Turkey’s corrections.

    Article Snippet: Cells were permeabilized with 0.1% Triton X100, blocked with 1.5% bovine serum albumin in PBS, and incubated at room temperature for 1 h. Samples were then washed in PBS and incubated with the primary antibody (rabbit polyclonal SOST antibody (Novus Biologicals, NBP1-77461)) (1: 100 dilution), overnight at 4 °C.

    Techniques: Staining, Fluorescence

    Fig. 6. Repopulation of adseverin-positive chondrocytes attenuated changes in Indian hedgehog and Runx2 expression despite increased proliferation, ap- optosis, collagen type X, and decreased aggrecan and F-actin. Immunohistochemical staining and quantification at 18 weeks of (A and B) adseverin, (C and D) Ihh, and (E and F) Ki67, as well as immunostaining for (G) aggrecan in the articular cartilage of Adseverin−/−and Adseverin+/+ mice. Scale bars, 200 μm. (H) Apoptotic chon- drocytes and the actin cytoskeleton were detected by immunofluorescent staining with TUNEL (green) and phalloidin (red), respectively. DAPI (blue) stains nuclei. Scale bar, 400 μm. Higher-magnification images of the red or white dashed box in regions are in fig. S6. (I) Quantification of TUNEL-positive cells in the articular cartilage of Adseverin−/−and Adseverin+/+ mice. Immunohistochemical staining of hypertrophic markers (J) Runx2 with (K) quantification and (L) collagen type X in the articular cartilage of Adseverin−/−versus Adseverin+/+ mice. Dot plots represent the mean with minimum and maximum values. Statistical analysis was assessed using Student’s unpaired two-tailed t test (B, D, F, I, and K). The number of biological replicates in each group and P values are indicated in the figure.

    Journal: Science advances

    Article Title: Adseverin, an actin-binding protein, modulates hypertrophic chondrocyte differentiation and osteoarthritis progression.

    doi: 10.1126/sciadv.adf1130

    Figure Lengend Snippet: Fig. 6. Repopulation of adseverin-positive chondrocytes attenuated changes in Indian hedgehog and Runx2 expression despite increased proliferation, ap- optosis, collagen type X, and decreased aggrecan and F-actin. Immunohistochemical staining and quantification at 18 weeks of (A and B) adseverin, (C and D) Ihh, and (E and F) Ki67, as well as immunostaining for (G) aggrecan in the articular cartilage of Adseverin−/−and Adseverin+/+ mice. Scale bars, 200 μm. (H) Apoptotic chon- drocytes and the actin cytoskeleton were detected by immunofluorescent staining with TUNEL (green) and phalloidin (red), respectively. DAPI (blue) stains nuclei. Scale bar, 400 μm. Higher-magnification images of the red or white dashed box in regions are in fig. S6. (I) Quantification of TUNEL-positive cells in the articular cartilage of Adseverin−/−and Adseverin+/+ mice. Immunohistochemical staining of hypertrophic markers (J) Runx2 with (K) quantification and (L) collagen type X in the articular cartilage of Adseverin−/−versus Adseverin+/+ mice. Dot plots represent the mean with minimum and maximum values. Statistical analysis was assessed using Student’s unpaired two-tailed t test (B, D, F, I, and K). The number of biological replicates in each group and P values are indicated in the figure.

    Article Snippet: Glogauer) (69), human adseverin (1:200; ab223055, Abcam), Ihh (1:100; ab39634, Abcam), Ki67 (1:50; ab15580, Abcam), αSMA (1:200; ab5694, Abcam), Runx2 (1:50; NBP1-77461, Novus Biologicals), MMP13 (1:200; 18165-1-AP, Proteintech), and collagen type X (1:1000; ab260040, Abcam).

    Techniques: Expressing, Immunohistochemical staining, Staining, Immunostaining, TUNEL Assay, Two Tailed Test