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alp activity measurement kit  (Beyotime)


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    Beyotime alp activity measurement kit
    M1 macrophages inhibit the osteogenic differentiation of BMSCs. ( A ) The M1 macrophage surface markers CD86 and CD11b were analysed via flow cytometry ( n = 3 independent experiments). ( B ) Diagram of M1 macrophage and BMSC coculture in vitro . ( C ) The mRNA levels of osteogenesis-related genes in BMSCs were determined via RT‒qPCR analyses ( n = 3 independent experiments). ( D ) Assessment of COL1a1 ( n = 3 independent experiments), RUNX2 ( n = 4 independent experiments) and BMP2 ( n = 4 independent experiments) expression in BMSCs from different treatment groups by Western blotting, with β-actin used for normalization and quantitative analysis by ImageJ. ( E ) Mineralization in treated BMSCs was evaluated by alizarin red staining and <t>ALP</t> staining ( n = 3 independent experiments). Scale bar: 100 μm. ( F ) Statistical data of Alizarin red staining. ( G ) Statistical data of the <t>ALP</t> <t>activity</t> assay ( n = 3 independent experiments). The data are presented as the means ± SD. ** P < 0.01, * P < 0.05, ns = not significant. One-way ANOVA followed by Holm-Sidak multiple comparison test
    Alp Activity Measurement Kit, supplied by Beyotime, 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/alp+measurement+kit/bcip+nbt+alp+color+development+kit/pmc11494760-289-0-14
    Average 90 stars, based on 1 article reviews
    alp activity measurement kit - by Bioz Stars, 2026-10
    90/100 stars

    Images

    1) Product Images from "Exosomal miR-1a-3p derived from glucocorticoid-stimulated M1 macrophages promotes the adipogenic differentiation of BMSCs in glucocorticoid-associated osteonecrosis of the femoral head by targeting Cebpz"

    Article Title: Exosomal miR-1a-3p derived from glucocorticoid-stimulated M1 macrophages promotes the adipogenic differentiation of BMSCs in glucocorticoid-associated osteonecrosis of the femoral head by targeting Cebpz

    Journal: Journal of Nanobiotechnology

    doi: 10.1186/s12951-024-02923-5

    M1 macrophages inhibit the osteogenic differentiation of BMSCs. ( A ) The M1 macrophage surface markers CD86 and CD11b were analysed via flow cytometry ( n = 3 independent experiments). ( B ) Diagram of M1 macrophage and BMSC coculture in vitro . ( C ) The mRNA levels of osteogenesis-related genes in BMSCs were determined via RT‒qPCR analyses ( n = 3 independent experiments). ( D ) Assessment of COL1a1 ( n = 3 independent experiments), RUNX2 ( n = 4 independent experiments) and BMP2 ( n = 4 independent experiments) expression in BMSCs from different treatment groups by Western blotting, with β-actin used for normalization and quantitative analysis by ImageJ. ( E ) Mineralization in treated BMSCs was evaluated by alizarin red staining and ALP staining ( n = 3 independent experiments). Scale bar: 100 μm. ( F ) Statistical data of Alizarin red staining. ( G ) Statistical data of the ALP activity assay ( n = 3 independent experiments). The data are presented as the means ± SD. ** P < 0.01, * P < 0.05, ns = not significant. One-way ANOVA followed by Holm-Sidak multiple comparison test
    Figure Legend Snippet: M1 macrophages inhibit the osteogenic differentiation of BMSCs. ( A ) The M1 macrophage surface markers CD86 and CD11b were analysed via flow cytometry ( n = 3 independent experiments). ( B ) Diagram of M1 macrophage and BMSC coculture in vitro . ( C ) The mRNA levels of osteogenesis-related genes in BMSCs were determined via RT‒qPCR analyses ( n = 3 independent experiments). ( D ) Assessment of COL1a1 ( n = 3 independent experiments), RUNX2 ( n = 4 independent experiments) and BMP2 ( n = 4 independent experiments) expression in BMSCs from different treatment groups by Western blotting, with β-actin used for normalization and quantitative analysis by ImageJ. ( E ) Mineralization in treated BMSCs was evaluated by alizarin red staining and ALP staining ( n = 3 independent experiments). Scale bar: 100 μm. ( F ) Statistical data of Alizarin red staining. ( G ) Statistical data of the ALP activity assay ( n = 3 independent experiments). The data are presented as the means ± SD. ** P < 0.01, * P < 0.05, ns = not significant. One-way ANOVA followed by Holm-Sidak multiple comparison test

    Techniques Used: Flow Cytometry, In Vitro, Expressing, Western Blot, Staining, ALP Activity Assay, Comparison

    M1 macrophage-derived exosomes inhibit the osteogenic differentiation of BMSCs. ( A ) Representative images of BMSCs cultured with n-M1-exos or GC-M1-exos for 12 h ( n = 3 independent experiments). DAPI (blue) indicates the nucleus, PKH26 (red) indicates the exosomes, and phalloidin (green) indicates the cytoskeleton. Scale bar: 4 μm. ( B ) The expression of COL1a1 in BMSCs from different treatment groups was evaluated by Western blotting and quantified using ImageJ ( n = 4 independent experiments). ( C ) Mineralization in treated BMSCs was evaluated by alizarin red staining and ALP staining ( n = 4 independent experiments). Scale bar: 100 μm. ( D ) The statistical data of Alizarin red staining. ( E ) The statistical data of ALP activity assay ( n = 3 independent experiments). ( F ) Transcriptome sequencing analysis of BMSCs from the different treatment groups: volcano maps and heatmaps showing differences in gene expression between the GC-M1-exos group and the n-M1-exos group compared with the control group. The data are presented as the mean ± SD. *** P < 0.001, ** P < 0.01, * P < 0.05, ns = not significant. One-way ANOVA followed by Holm-Sidak multiple comparison test
    Figure Legend Snippet: M1 macrophage-derived exosomes inhibit the osteogenic differentiation of BMSCs. ( A ) Representative images of BMSCs cultured with n-M1-exos or GC-M1-exos for 12 h ( n = 3 independent experiments). DAPI (blue) indicates the nucleus, PKH26 (red) indicates the exosomes, and phalloidin (green) indicates the cytoskeleton. Scale bar: 4 μm. ( B ) The expression of COL1a1 in BMSCs from different treatment groups was evaluated by Western blotting and quantified using ImageJ ( n = 4 independent experiments). ( C ) Mineralization in treated BMSCs was evaluated by alizarin red staining and ALP staining ( n = 4 independent experiments). Scale bar: 100 μm. ( D ) The statistical data of Alizarin red staining. ( E ) The statistical data of ALP activity assay ( n = 3 independent experiments). ( F ) Transcriptome sequencing analysis of BMSCs from the different treatment groups: volcano maps and heatmaps showing differences in gene expression between the GC-M1-exos group and the n-M1-exos group compared with the control group. The data are presented as the mean ± SD. *** P < 0.001, ** P < 0.01, * P < 0.05, ns = not significant. One-way ANOVA followed by Holm-Sidak multiple comparison test

    Techniques Used: Derivative Assay, Cell Culture, Expressing, Western Blot, Staining, ALP Activity Assay, Sequencing, Gene Expression, Control, Comparison

    Related Articles

    Activity Assay:

    Article Title: Connexin 43 Modulates Osteogenic Differentiation of Bone Marrow Stromal Cells Through GSK-3beta/Beta-Catenin Signaling Pathways.
    Article Snippet: Published by S. Karger AG, Basel www.karger.com/cpb Lin et al.: Cx43 Modulates Osteogenic Differentiation Quantitation of ALP activity ALP activity is elevated early following induction of differentiation, but decreases at later stages, so we choose the 9-day time point to determine ALP activity. .. Activity was measured using an ALP measurement kit (Beyotime, # P0321). ..

    Article Title: Quercetin stimulates osteogenic differentiation of bone marrow stromal cells through miRNA-206/connexin 43 pathway
    Article Snippet: .. Alkaline phosphatase (ALP) activity assay At the designated time, ALP activity was evaluated using an ALP measurement kit (Beyotime, #P0321). ..

    ALP Activity Assay:

    Article Title: Quercetin stimulates osteogenic differentiation of bone marrow stromal cells through miRNA-206/connexin 43 pathway
    Article Snippet: .. Alkaline phosphatase (ALP) activity assay At the designated time, ALP activity was evaluated using an ALP measurement kit (Beyotime, #P0321). ..



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    M1 macrophages inhibit the osteogenic differentiation of BMSCs. ( A ) The M1 macrophage surface markers CD86 and CD11b were analysed via flow cytometry ( n = 3 independent experiments). ( B ) Diagram of M1 macrophage and BMSC coculture in vitro . ( C ) The mRNA levels of osteogenesis-related genes in BMSCs were determined via RT‒qPCR analyses ( n = 3 independent experiments). ( D ) Assessment of COL1a1 ( n = 3 independent experiments), RUNX2 ( n = 4 independent experiments) and BMP2 ( n = 4 independent experiments) expression in BMSCs from different treatment groups by Western blotting, with β-actin used for normalization and quantitative analysis by ImageJ. ( E ) Mineralization in treated BMSCs was evaluated by alizarin red staining and <t>ALP</t> staining ( n = 3 independent experiments). Scale bar: 100 μm. ( F ) Statistical data of Alizarin red staining. ( G ) Statistical data of the <t>ALP</t> <t>activity</t> assay ( n = 3 independent experiments). The data are presented as the means ± SD. ** P < 0.01, * P < 0.05, ns = not significant. One-way ANOVA followed by Holm-Sidak multiple comparison test
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    M1 macrophages inhibit the osteogenic differentiation of BMSCs. ( A ) The M1 macrophage surface markers CD86 and CD11b were analysed via flow cytometry ( n = 3 independent experiments). ( B ) Diagram of M1 macrophage and BMSC coculture in vitro . ( C ) The mRNA levels of osteogenesis-related genes in BMSCs were determined via RT‒qPCR analyses ( n = 3 independent experiments). ( D ) Assessment of COL1a1 ( n = 3 independent experiments), RUNX2 ( n = 4 independent experiments) and BMP2 ( n = 4 independent experiments) expression in BMSCs from different treatment groups by Western blotting, with β-actin used for normalization and quantitative analysis by ImageJ. ( E ) Mineralization in treated BMSCs was evaluated by alizarin red staining and <t>ALP</t> staining ( n = 3 independent experiments). Scale bar: 100 μm. ( F ) Statistical data of Alizarin red staining. ( G ) Statistical data of the <t>ALP</t> <t>activity</t> assay ( n = 3 independent experiments). The data are presented as the means ± SD. ** P < 0.01, * P < 0.05, ns = not significant. One-way ANOVA followed by Holm-Sidak multiple comparison test
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    Image Search Results


    M1 macrophages inhibit the osteogenic differentiation of BMSCs. ( A ) The M1 macrophage surface markers CD86 and CD11b were analysed via flow cytometry ( n = 3 independent experiments). ( B ) Diagram of M1 macrophage and BMSC coculture in vitro . ( C ) The mRNA levels of osteogenesis-related genes in BMSCs were determined via RT‒qPCR analyses ( n = 3 independent experiments). ( D ) Assessment of COL1a1 ( n = 3 independent experiments), RUNX2 ( n = 4 independent experiments) and BMP2 ( n = 4 independent experiments) expression in BMSCs from different treatment groups by Western blotting, with β-actin used for normalization and quantitative analysis by ImageJ. ( E ) Mineralization in treated BMSCs was evaluated by alizarin red staining and ALP staining ( n = 3 independent experiments). Scale bar: 100 μm. ( F ) Statistical data of Alizarin red staining. ( G ) Statistical data of the ALP activity assay ( n = 3 independent experiments). The data are presented as the means ± SD. ** P < 0.01, * P < 0.05, ns = not significant. One-way ANOVA followed by Holm-Sidak multiple comparison test

    Journal: Journal of Nanobiotechnology

    Article Title: Exosomal miR-1a-3p derived from glucocorticoid-stimulated M1 macrophages promotes the adipogenic differentiation of BMSCs in glucocorticoid-associated osteonecrosis of the femoral head by targeting Cebpz

    doi: 10.1186/s12951-024-02923-5

    Figure Lengend Snippet: M1 macrophages inhibit the osteogenic differentiation of BMSCs. ( A ) The M1 macrophage surface markers CD86 and CD11b were analysed via flow cytometry ( n = 3 independent experiments). ( B ) Diagram of M1 macrophage and BMSC coculture in vitro . ( C ) The mRNA levels of osteogenesis-related genes in BMSCs were determined via RT‒qPCR analyses ( n = 3 independent experiments). ( D ) Assessment of COL1a1 ( n = 3 independent experiments), RUNX2 ( n = 4 independent experiments) and BMP2 ( n = 4 independent experiments) expression in BMSCs from different treatment groups by Western blotting, with β-actin used for normalization and quantitative analysis by ImageJ. ( E ) Mineralization in treated BMSCs was evaluated by alizarin red staining and ALP staining ( n = 3 independent experiments). Scale bar: 100 μm. ( F ) Statistical data of Alizarin red staining. ( G ) Statistical data of the ALP activity assay ( n = 3 independent experiments). The data are presented as the means ± SD. ** P < 0.01, * P < 0.05, ns = not significant. One-way ANOVA followed by Holm-Sidak multiple comparison test

    Article Snippet: ALP activity was quantitatively measured using a commercial kit following the manufacturer’s instructions (P0321M, Beyotime).

    Techniques: Flow Cytometry, In Vitro, Expressing, Western Blot, Staining, ALP Activity Assay, Comparison

    M1 macrophage-derived exosomes inhibit the osteogenic differentiation of BMSCs. ( A ) Representative images of BMSCs cultured with n-M1-exos or GC-M1-exos for 12 h ( n = 3 independent experiments). DAPI (blue) indicates the nucleus, PKH26 (red) indicates the exosomes, and phalloidin (green) indicates the cytoskeleton. Scale bar: 4 μm. ( B ) The expression of COL1a1 in BMSCs from different treatment groups was evaluated by Western blotting and quantified using ImageJ ( n = 4 independent experiments). ( C ) Mineralization in treated BMSCs was evaluated by alizarin red staining and ALP staining ( n = 4 independent experiments). Scale bar: 100 μm. ( D ) The statistical data of Alizarin red staining. ( E ) The statistical data of ALP activity assay ( n = 3 independent experiments). ( F ) Transcriptome sequencing analysis of BMSCs from the different treatment groups: volcano maps and heatmaps showing differences in gene expression between the GC-M1-exos group and the n-M1-exos group compared with the control group. The data are presented as the mean ± SD. *** P < 0.001, ** P < 0.01, * P < 0.05, ns = not significant. One-way ANOVA followed by Holm-Sidak multiple comparison test

    Journal: Journal of Nanobiotechnology

    Article Title: Exosomal miR-1a-3p derived from glucocorticoid-stimulated M1 macrophages promotes the adipogenic differentiation of BMSCs in glucocorticoid-associated osteonecrosis of the femoral head by targeting Cebpz

    doi: 10.1186/s12951-024-02923-5

    Figure Lengend Snippet: M1 macrophage-derived exosomes inhibit the osteogenic differentiation of BMSCs. ( A ) Representative images of BMSCs cultured with n-M1-exos or GC-M1-exos for 12 h ( n = 3 independent experiments). DAPI (blue) indicates the nucleus, PKH26 (red) indicates the exosomes, and phalloidin (green) indicates the cytoskeleton. Scale bar: 4 μm. ( B ) The expression of COL1a1 in BMSCs from different treatment groups was evaluated by Western blotting and quantified using ImageJ ( n = 4 independent experiments). ( C ) Mineralization in treated BMSCs was evaluated by alizarin red staining and ALP staining ( n = 4 independent experiments). Scale bar: 100 μm. ( D ) The statistical data of Alizarin red staining. ( E ) The statistical data of ALP activity assay ( n = 3 independent experiments). ( F ) Transcriptome sequencing analysis of BMSCs from the different treatment groups: volcano maps and heatmaps showing differences in gene expression between the GC-M1-exos group and the n-M1-exos group compared with the control group. The data are presented as the mean ± SD. *** P < 0.001, ** P < 0.01, * P < 0.05, ns = not significant. One-way ANOVA followed by Holm-Sidak multiple comparison test

    Article Snippet: ALP activity was quantitatively measured using a commercial kit following the manufacturer’s instructions (P0321M, Beyotime).

    Techniques: Derivative Assay, Cell Culture, Expressing, Western Blot, Staining, ALP Activity Assay, Sequencing, Gene Expression, Control, Comparison