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rabbit anti-bmp2 antibody  (ABclonal Biotechnology)


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    ABclonal Biotechnology rabbit anti-bmp2 antibody
    Osteogenesis and lactylation levels are decreased in inflamed periodontal tissue and LPS-stimulated PDLSCs. ( A ) H&E staining in rat periodontal tissues and immunohistochemical Pan Kla and RUNX2 expression. ( B ) Quantitative analysis of positive areas. ( C ) Western blotting showing protein levels of COL-1, ALP, RUNX2, and <t>BMP2</t> in LPS-treated PDLSCs. ( D ) qRT-PCR showing mRNA levels of osteogenic genes COL-1 , ALP, RUNX2 , and BMP2 . ( E ) ALP staining at 7 days and ARS staining at 21 days of osteogenic induction in LPS-treated PDLSCs. ( F ) Lactate concentration in the culture medium of PDLSCs was measured at the indicated times, as shown in the quantitative analysis. ( G ) Western blotting showing the protein level of Pan Kla in LPS-treated PDLSCs. ( H ) Quantitative analysis of Pan Kla protein levels. ( I ) Immunofluorescence staining images showing the expression levels of RUNX2 (green) and Pan Kla (red) in PDLSCs after LPS treatment. Cell nuclei were stained with DAPI (blue). PDLSCs: periodontal ligament stem cells; Kla: lysine lactylation; LPS: lipopolysaccharide; NC: healthy mice without periodontitis; H&E: hematoxylin and eosin staining (Data are expressed as mean ± SD, N = 3. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, NS indicates no statistical difference).
    Rabbit Anti Bmp2 Antibody, supplied by ABclonal Biotechnology, 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/rabbit+anti-bmp2+antibody/pmc10931601-184-36-40?v=ABclonal+Biotechnology
    Average 90 stars, based on 1 article reviews
    rabbit anti-bmp2 antibody - by Bioz Stars, 2026-07
    90/100 stars

    Images

    1) Product Images from "Proanthocyanidins Ameliorate LPS-Inhibited Osteogenesis of PDLSCs by Restoring Lysine Lactylation"

    Article Title: Proanthocyanidins Ameliorate LPS-Inhibited Osteogenesis of PDLSCs by Restoring Lysine Lactylation

    Journal: International Journal of Molecular Sciences

    doi: 10.3390/ijms25052947

    Osteogenesis and lactylation levels are decreased in inflamed periodontal tissue and LPS-stimulated PDLSCs. ( A ) H&E staining in rat periodontal tissues and immunohistochemical Pan Kla and RUNX2 expression. ( B ) Quantitative analysis of positive areas. ( C ) Western blotting showing protein levels of COL-1, ALP, RUNX2, and BMP2 in LPS-treated PDLSCs. ( D ) qRT-PCR showing mRNA levels of osteogenic genes COL-1 , ALP, RUNX2 , and BMP2 . ( E ) ALP staining at 7 days and ARS staining at 21 days of osteogenic induction in LPS-treated PDLSCs. ( F ) Lactate concentration in the culture medium of PDLSCs was measured at the indicated times, as shown in the quantitative analysis. ( G ) Western blotting showing the protein level of Pan Kla in LPS-treated PDLSCs. ( H ) Quantitative analysis of Pan Kla protein levels. ( I ) Immunofluorescence staining images showing the expression levels of RUNX2 (green) and Pan Kla (red) in PDLSCs after LPS treatment. Cell nuclei were stained with DAPI (blue). PDLSCs: periodontal ligament stem cells; Kla: lysine lactylation; LPS: lipopolysaccharide; NC: healthy mice without periodontitis; H&E: hematoxylin and eosin staining (Data are expressed as mean ± SD, N = 3. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, NS indicates no statistical difference).
    Figure Legend Snippet: Osteogenesis and lactylation levels are decreased in inflamed periodontal tissue and LPS-stimulated PDLSCs. ( A ) H&E staining in rat periodontal tissues and immunohistochemical Pan Kla and RUNX2 expression. ( B ) Quantitative analysis of positive areas. ( C ) Western blotting showing protein levels of COL-1, ALP, RUNX2, and BMP2 in LPS-treated PDLSCs. ( D ) qRT-PCR showing mRNA levels of osteogenic genes COL-1 , ALP, RUNX2 , and BMP2 . ( E ) ALP staining at 7 days and ARS staining at 21 days of osteogenic induction in LPS-treated PDLSCs. ( F ) Lactate concentration in the culture medium of PDLSCs was measured at the indicated times, as shown in the quantitative analysis. ( G ) Western blotting showing the protein level of Pan Kla in LPS-treated PDLSCs. ( H ) Quantitative analysis of Pan Kla protein levels. ( I ) Immunofluorescence staining images showing the expression levels of RUNX2 (green) and Pan Kla (red) in PDLSCs after LPS treatment. Cell nuclei were stained with DAPI (blue). PDLSCs: periodontal ligament stem cells; Kla: lysine lactylation; LPS: lipopolysaccharide; NC: healthy mice without periodontitis; H&E: hematoxylin and eosin staining (Data are expressed as mean ± SD, N = 3. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, NS indicates no statistical difference).

    Techniques Used: Staining, Immunohistochemical staining, Expressing, Western Blot, Quantitative RT-PCR, Concentration Assay, Immunofluorescence

    Restoration of lactylation by TSA recovers the osteogenesis of PDLSCs in an inflammatory state. ( A ) Western blotting showing the protein levels of COL-1, ALP, RUNX2, and BMP2 in PDLSCs after treatment with the conditions as shown. ( B ) Quantification of protein levels of COL-1, ALP, RUNX2, and BMP2. ( C ) qRT-PCR showing mRNA levels of osteogenic genes COL-1 , ALP, RUNX2, and BMP2 . ( D ) ALP staining at 7 days and ARS staining at 21 days of osteogenic induction in PDLSCs. ( E ) Quantitative analysis of ALP staining and ARS staining. ( F ) Immunofluorescence staining images showing the expression levels of RUNX2 (green) and Pan Kla (red) in PDLSCs treated with the conditions as shown. Cell nuclei were stained with DAPI (blue). ( G ) Pearson linear regression analysis of RUNX2 and Pan Ka fluorescence intensity. PDLSCs: periodontal ligament stem cells; Kla: lysine lactylation; LPS: lipopolysaccharide; TSA: Trichostatin A (Data are expressed as mean ± SD, N = 3. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, NS indicates no statistical difference).
    Figure Legend Snippet: Restoration of lactylation by TSA recovers the osteogenesis of PDLSCs in an inflammatory state. ( A ) Western blotting showing the protein levels of COL-1, ALP, RUNX2, and BMP2 in PDLSCs after treatment with the conditions as shown. ( B ) Quantification of protein levels of COL-1, ALP, RUNX2, and BMP2. ( C ) qRT-PCR showing mRNA levels of osteogenic genes COL-1 , ALP, RUNX2, and BMP2 . ( D ) ALP staining at 7 days and ARS staining at 21 days of osteogenic induction in PDLSCs. ( E ) Quantitative analysis of ALP staining and ARS staining. ( F ) Immunofluorescence staining images showing the expression levels of RUNX2 (green) and Pan Kla (red) in PDLSCs treated with the conditions as shown. Cell nuclei were stained with DAPI (blue). ( G ) Pearson linear regression analysis of RUNX2 and Pan Ka fluorescence intensity. PDLSCs: periodontal ligament stem cells; Kla: lysine lactylation; LPS: lipopolysaccharide; TSA: Trichostatin A (Data are expressed as mean ± SD, N = 3. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, NS indicates no statistical difference).

    Techniques Used: Western Blot, Quantitative RT-PCR, Staining, Immunofluorescence, Expressing, Fluorescence

    Proanthocyanidins promote osteogenesis and elevate the lactylation of PDLSCs. ( A ) Western blotting showing protein levels of COL-1, ALP, RUNX2, and BMP2 in PA-treated PDLSCs. ( B ) Quantification of protein levels of COL-1, ALP, RUNX2, and BMP2. ( C ) qRT-PCR showing mRNA levels of osteogenic genes COL-1 , ALP, RUNX2 , and BMP2 . ( D ) ALP staining at 7 days and ARS staining at 21 days of osteogenic induction in PA-treated PDLSCs. ( E ) Lactate concentration in the culture medium of PDLSCs was measured at the indicated times as shown in the quantitative analysis. ( F ) Western blotting showing the protein level of Pan Kla in PA-treated PDLSCs. ( G ) Quantitative analysis of Pan Kla protein levels. ( H ) Immunofluorescence staining images showing the expression levels of RUNX2 (green) and Pan Kla (red) in PDLSCs after treatment with the conditions as shown. Cell nuclei were stained with DAPI (blue). PDLSCs: periodontal ligament stem cells; Kla: lysine lactylation; PA: proanthocyanidins (Data are expressed as mean ± SD, N = 3. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, NS indicates no statistical difference).
    Figure Legend Snippet: Proanthocyanidins promote osteogenesis and elevate the lactylation of PDLSCs. ( A ) Western blotting showing protein levels of COL-1, ALP, RUNX2, and BMP2 in PA-treated PDLSCs. ( B ) Quantification of protein levels of COL-1, ALP, RUNX2, and BMP2. ( C ) qRT-PCR showing mRNA levels of osteogenic genes COL-1 , ALP, RUNX2 , and BMP2 . ( D ) ALP staining at 7 days and ARS staining at 21 days of osteogenic induction in PA-treated PDLSCs. ( E ) Lactate concentration in the culture medium of PDLSCs was measured at the indicated times as shown in the quantitative analysis. ( F ) Western blotting showing the protein level of Pan Kla in PA-treated PDLSCs. ( G ) Quantitative analysis of Pan Kla protein levels. ( H ) Immunofluorescence staining images showing the expression levels of RUNX2 (green) and Pan Kla (red) in PDLSCs after treatment with the conditions as shown. Cell nuclei were stained with DAPI (blue). PDLSCs: periodontal ligament stem cells; Kla: lysine lactylation; PA: proanthocyanidins (Data are expressed as mean ± SD, N = 3. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, NS indicates no statistical difference).

    Techniques Used: Western Blot, Quantitative RT-PCR, Staining, Concentration Assay, Immunofluorescence, Expressing

    Proanthocyanidins recover PDLSC osteogenesis by restoring the lactylation of PDLSCs in an inflammatory state. ( A ) Western blotting showing the protein levels of COL-1, ALP, RUNX2, and BMP2 in PDLSCs after treatment with the conditions as shown. ( B ) Quantification of protein levels of COL-1, ALP, RUNX2, and BMP2. ( C ) qRT-PCR showing mRNA levels of osteogenic genes COL-1 , ALP, RUNX2, and BMP2 . ( D ) ALP staining at 7 days and ARS staining at 21 days of osteogenic induction in PDLSCs. ( E ) Quantitative analysis of ALP staining and ARS staining. ( F ) Immunofluorescence staining images showing the expression levels of RUNX2 (green) and Pan Kla (red) in PDLSCs treated with the conditions as shown. Cell nuclei were stained with DAPI (blue). ( G ) Pearson linear regression analysis of RUNX2 and Pan Ka fluorescence intensity. PDLSCs: periodontal ligament stem cells; Kla: lysine lactylation; PA: proanthocyanidins; Theo-24: theophylline (Data are expressed as mean ± SD, N = 3. * p < 0.05, ** p < 0.01, *** p < 0.001, NS indicates no statistical difference).
    Figure Legend Snippet: Proanthocyanidins recover PDLSC osteogenesis by restoring the lactylation of PDLSCs in an inflammatory state. ( A ) Western blotting showing the protein levels of COL-1, ALP, RUNX2, and BMP2 in PDLSCs after treatment with the conditions as shown. ( B ) Quantification of protein levels of COL-1, ALP, RUNX2, and BMP2. ( C ) qRT-PCR showing mRNA levels of osteogenic genes COL-1 , ALP, RUNX2, and BMP2 . ( D ) ALP staining at 7 days and ARS staining at 21 days of osteogenic induction in PDLSCs. ( E ) Quantitative analysis of ALP staining and ARS staining. ( F ) Immunofluorescence staining images showing the expression levels of RUNX2 (green) and Pan Kla (red) in PDLSCs treated with the conditions as shown. Cell nuclei were stained with DAPI (blue). ( G ) Pearson linear regression analysis of RUNX2 and Pan Ka fluorescence intensity. PDLSCs: periodontal ligament stem cells; Kla: lysine lactylation; PA: proanthocyanidins; Theo-24: theophylline (Data are expressed as mean ± SD, N = 3. * p < 0.05, ** p < 0.01, *** p < 0.001, NS indicates no statistical difference).

    Techniques Used: Western Blot, Quantitative RT-PCR, Staining, Immunofluorescence, Expressing, Fluorescence

    Primer sequences.
    Figure Legend Snippet: Primer sequences.

    Techniques Used:



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    Osteogenesis and lactylation levels are decreased in inflamed periodontal tissue and LPS-stimulated PDLSCs. ( A ) H&E staining in rat periodontal tissues and immunohistochemical Pan Kla and RUNX2 expression. ( B ) Quantitative analysis of positive areas. ( C ) Western blotting showing protein levels of COL-1, ALP, RUNX2, and <t>BMP2</t> in LPS-treated PDLSCs. ( D ) qRT-PCR showing mRNA levels of osteogenic genes COL-1 , ALP, RUNX2 , and BMP2 . ( E ) ALP staining at 7 days and ARS staining at 21 days of osteogenic induction in LPS-treated PDLSCs. ( F ) Lactate concentration in the culture medium of PDLSCs was measured at the indicated times, as shown in the quantitative analysis. ( G ) Western blotting showing the protein level of Pan Kla in LPS-treated PDLSCs. ( H ) Quantitative analysis of Pan Kla protein levels. ( I ) Immunofluorescence staining images showing the expression levels of RUNX2 (green) and Pan Kla (red) in PDLSCs after LPS treatment. Cell nuclei were stained with DAPI (blue). PDLSCs: periodontal ligament stem cells; Kla: lysine lactylation; LPS: lipopolysaccharide; NC: healthy mice without periodontitis; H&E: hematoxylin and eosin staining (Data are expressed as mean ± SD, N = 3. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, NS indicates no statistical difference).
    Rabbit Anti Bmp2 Antibody, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Osteogenesis and lactylation levels are decreased in inflamed periodontal tissue and LPS-stimulated PDLSCs. ( A ) H&E staining in rat periodontal tissues and immunohistochemical Pan Kla and RUNX2 expression. ( B ) Quantitative analysis of positive areas. ( C ) Western blotting showing protein levels of COL-1, ALP, RUNX2, and BMP2 in LPS-treated PDLSCs. ( D ) qRT-PCR showing mRNA levels of osteogenic genes COL-1 , ALP, RUNX2 , and BMP2 . ( E ) ALP staining at 7 days and ARS staining at 21 days of osteogenic induction in LPS-treated PDLSCs. ( F ) Lactate concentration in the culture medium of PDLSCs was measured at the indicated times, as shown in the quantitative analysis. ( G ) Western blotting showing the protein level of Pan Kla in LPS-treated PDLSCs. ( H ) Quantitative analysis of Pan Kla protein levels. ( I ) Immunofluorescence staining images showing the expression levels of RUNX2 (green) and Pan Kla (red) in PDLSCs after LPS treatment. Cell nuclei were stained with DAPI (blue). PDLSCs: periodontal ligament stem cells; Kla: lysine lactylation; LPS: lipopolysaccharide; NC: healthy mice without periodontitis; H&E: hematoxylin and eosin staining (Data are expressed as mean ± SD, N = 3. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, NS indicates no statistical difference).

    Journal: International Journal of Molecular Sciences

    Article Title: Proanthocyanidins Ameliorate LPS-Inhibited Osteogenesis of PDLSCs by Restoring Lysine Lactylation

    doi: 10.3390/ijms25052947

    Figure Lengend Snippet: Osteogenesis and lactylation levels are decreased in inflamed periodontal tissue and LPS-stimulated PDLSCs. ( A ) H&E staining in rat periodontal tissues and immunohistochemical Pan Kla and RUNX2 expression. ( B ) Quantitative analysis of positive areas. ( C ) Western blotting showing protein levels of COL-1, ALP, RUNX2, and BMP2 in LPS-treated PDLSCs. ( D ) qRT-PCR showing mRNA levels of osteogenic genes COL-1 , ALP, RUNX2 , and BMP2 . ( E ) ALP staining at 7 days and ARS staining at 21 days of osteogenic induction in LPS-treated PDLSCs. ( F ) Lactate concentration in the culture medium of PDLSCs was measured at the indicated times, as shown in the quantitative analysis. ( G ) Western blotting showing the protein level of Pan Kla in LPS-treated PDLSCs. ( H ) Quantitative analysis of Pan Kla protein levels. ( I ) Immunofluorescence staining images showing the expression levels of RUNX2 (green) and Pan Kla (red) in PDLSCs after LPS treatment. Cell nuclei were stained with DAPI (blue). PDLSCs: periodontal ligament stem cells; Kla: lysine lactylation; LPS: lipopolysaccharide; NC: healthy mice without periodontitis; H&E: hematoxylin and eosin staining (Data are expressed as mean ± SD, N = 3. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, NS indicates no statistical difference).

    Article Snippet: Primary antibodies are as follows: rabbit ant-IL-1β (1:1000, Cell Signaling Technology, Danvers, MA, USA); rabbit anti-coll I antibody (1:1000, ABclonal, Wuhan, China); rabbit anti-ALP antibody (1:1000, ABclonal, Wuhan, China); rabbit anti-RUNX2 antibody (1:1000, ABclonal, Wuhan, China); rabbit anti-BMP2 antibody (1:1000, ABclonal, Wuhan, China); and rabbit anti-Pan Kla antibody (1:1000, PTM Bio, Hangzhou, China).

    Techniques: Staining, Immunohistochemical staining, Expressing, Western Blot, Quantitative RT-PCR, Concentration Assay, Immunofluorescence

    Restoration of lactylation by TSA recovers the osteogenesis of PDLSCs in an inflammatory state. ( A ) Western blotting showing the protein levels of COL-1, ALP, RUNX2, and BMP2 in PDLSCs after treatment with the conditions as shown. ( B ) Quantification of protein levels of COL-1, ALP, RUNX2, and BMP2. ( C ) qRT-PCR showing mRNA levels of osteogenic genes COL-1 , ALP, RUNX2, and BMP2 . ( D ) ALP staining at 7 days and ARS staining at 21 days of osteogenic induction in PDLSCs. ( E ) Quantitative analysis of ALP staining and ARS staining. ( F ) Immunofluorescence staining images showing the expression levels of RUNX2 (green) and Pan Kla (red) in PDLSCs treated with the conditions as shown. Cell nuclei were stained with DAPI (blue). ( G ) Pearson linear regression analysis of RUNX2 and Pan Ka fluorescence intensity. PDLSCs: periodontal ligament stem cells; Kla: lysine lactylation; LPS: lipopolysaccharide; TSA: Trichostatin A (Data are expressed as mean ± SD, N = 3. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, NS indicates no statistical difference).

    Journal: International Journal of Molecular Sciences

    Article Title: Proanthocyanidins Ameliorate LPS-Inhibited Osteogenesis of PDLSCs by Restoring Lysine Lactylation

    doi: 10.3390/ijms25052947

    Figure Lengend Snippet: Restoration of lactylation by TSA recovers the osteogenesis of PDLSCs in an inflammatory state. ( A ) Western blotting showing the protein levels of COL-1, ALP, RUNX2, and BMP2 in PDLSCs after treatment with the conditions as shown. ( B ) Quantification of protein levels of COL-1, ALP, RUNX2, and BMP2. ( C ) qRT-PCR showing mRNA levels of osteogenic genes COL-1 , ALP, RUNX2, and BMP2 . ( D ) ALP staining at 7 days and ARS staining at 21 days of osteogenic induction in PDLSCs. ( E ) Quantitative analysis of ALP staining and ARS staining. ( F ) Immunofluorescence staining images showing the expression levels of RUNX2 (green) and Pan Kla (red) in PDLSCs treated with the conditions as shown. Cell nuclei were stained with DAPI (blue). ( G ) Pearson linear regression analysis of RUNX2 and Pan Ka fluorescence intensity. PDLSCs: periodontal ligament stem cells; Kla: lysine lactylation; LPS: lipopolysaccharide; TSA: Trichostatin A (Data are expressed as mean ± SD, N = 3. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, NS indicates no statistical difference).

    Article Snippet: Primary antibodies are as follows: rabbit ant-IL-1β (1:1000, Cell Signaling Technology, Danvers, MA, USA); rabbit anti-coll I antibody (1:1000, ABclonal, Wuhan, China); rabbit anti-ALP antibody (1:1000, ABclonal, Wuhan, China); rabbit anti-RUNX2 antibody (1:1000, ABclonal, Wuhan, China); rabbit anti-BMP2 antibody (1:1000, ABclonal, Wuhan, China); and rabbit anti-Pan Kla antibody (1:1000, PTM Bio, Hangzhou, China).

    Techniques: Western Blot, Quantitative RT-PCR, Staining, Immunofluorescence, Expressing, Fluorescence

    Proanthocyanidins promote osteogenesis and elevate the lactylation of PDLSCs. ( A ) Western blotting showing protein levels of COL-1, ALP, RUNX2, and BMP2 in PA-treated PDLSCs. ( B ) Quantification of protein levels of COL-1, ALP, RUNX2, and BMP2. ( C ) qRT-PCR showing mRNA levels of osteogenic genes COL-1 , ALP, RUNX2 , and BMP2 . ( D ) ALP staining at 7 days and ARS staining at 21 days of osteogenic induction in PA-treated PDLSCs. ( E ) Lactate concentration in the culture medium of PDLSCs was measured at the indicated times as shown in the quantitative analysis. ( F ) Western blotting showing the protein level of Pan Kla in PA-treated PDLSCs. ( G ) Quantitative analysis of Pan Kla protein levels. ( H ) Immunofluorescence staining images showing the expression levels of RUNX2 (green) and Pan Kla (red) in PDLSCs after treatment with the conditions as shown. Cell nuclei were stained with DAPI (blue). PDLSCs: periodontal ligament stem cells; Kla: lysine lactylation; PA: proanthocyanidins (Data are expressed as mean ± SD, N = 3. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, NS indicates no statistical difference).

    Journal: International Journal of Molecular Sciences

    Article Title: Proanthocyanidins Ameliorate LPS-Inhibited Osteogenesis of PDLSCs by Restoring Lysine Lactylation

    doi: 10.3390/ijms25052947

    Figure Lengend Snippet: Proanthocyanidins promote osteogenesis and elevate the lactylation of PDLSCs. ( A ) Western blotting showing protein levels of COL-1, ALP, RUNX2, and BMP2 in PA-treated PDLSCs. ( B ) Quantification of protein levels of COL-1, ALP, RUNX2, and BMP2. ( C ) qRT-PCR showing mRNA levels of osteogenic genes COL-1 , ALP, RUNX2 , and BMP2 . ( D ) ALP staining at 7 days and ARS staining at 21 days of osteogenic induction in PA-treated PDLSCs. ( E ) Lactate concentration in the culture medium of PDLSCs was measured at the indicated times as shown in the quantitative analysis. ( F ) Western blotting showing the protein level of Pan Kla in PA-treated PDLSCs. ( G ) Quantitative analysis of Pan Kla protein levels. ( H ) Immunofluorescence staining images showing the expression levels of RUNX2 (green) and Pan Kla (red) in PDLSCs after treatment with the conditions as shown. Cell nuclei were stained with DAPI (blue). PDLSCs: periodontal ligament stem cells; Kla: lysine lactylation; PA: proanthocyanidins (Data are expressed as mean ± SD, N = 3. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, NS indicates no statistical difference).

    Article Snippet: Primary antibodies are as follows: rabbit ant-IL-1β (1:1000, Cell Signaling Technology, Danvers, MA, USA); rabbit anti-coll I antibody (1:1000, ABclonal, Wuhan, China); rabbit anti-ALP antibody (1:1000, ABclonal, Wuhan, China); rabbit anti-RUNX2 antibody (1:1000, ABclonal, Wuhan, China); rabbit anti-BMP2 antibody (1:1000, ABclonal, Wuhan, China); and rabbit anti-Pan Kla antibody (1:1000, PTM Bio, Hangzhou, China).

    Techniques: Western Blot, Quantitative RT-PCR, Staining, Concentration Assay, Immunofluorescence, Expressing

    Proanthocyanidins recover PDLSC osteogenesis by restoring the lactylation of PDLSCs in an inflammatory state. ( A ) Western blotting showing the protein levels of COL-1, ALP, RUNX2, and BMP2 in PDLSCs after treatment with the conditions as shown. ( B ) Quantification of protein levels of COL-1, ALP, RUNX2, and BMP2. ( C ) qRT-PCR showing mRNA levels of osteogenic genes COL-1 , ALP, RUNX2, and BMP2 . ( D ) ALP staining at 7 days and ARS staining at 21 days of osteogenic induction in PDLSCs. ( E ) Quantitative analysis of ALP staining and ARS staining. ( F ) Immunofluorescence staining images showing the expression levels of RUNX2 (green) and Pan Kla (red) in PDLSCs treated with the conditions as shown. Cell nuclei were stained with DAPI (blue). ( G ) Pearson linear regression analysis of RUNX2 and Pan Ka fluorescence intensity. PDLSCs: periodontal ligament stem cells; Kla: lysine lactylation; PA: proanthocyanidins; Theo-24: theophylline (Data are expressed as mean ± SD, N = 3. * p < 0.05, ** p < 0.01, *** p < 0.001, NS indicates no statistical difference).

    Journal: International Journal of Molecular Sciences

    Article Title: Proanthocyanidins Ameliorate LPS-Inhibited Osteogenesis of PDLSCs by Restoring Lysine Lactylation

    doi: 10.3390/ijms25052947

    Figure Lengend Snippet: Proanthocyanidins recover PDLSC osteogenesis by restoring the lactylation of PDLSCs in an inflammatory state. ( A ) Western blotting showing the protein levels of COL-1, ALP, RUNX2, and BMP2 in PDLSCs after treatment with the conditions as shown. ( B ) Quantification of protein levels of COL-1, ALP, RUNX2, and BMP2. ( C ) qRT-PCR showing mRNA levels of osteogenic genes COL-1 , ALP, RUNX2, and BMP2 . ( D ) ALP staining at 7 days and ARS staining at 21 days of osteogenic induction in PDLSCs. ( E ) Quantitative analysis of ALP staining and ARS staining. ( F ) Immunofluorescence staining images showing the expression levels of RUNX2 (green) and Pan Kla (red) in PDLSCs treated with the conditions as shown. Cell nuclei were stained with DAPI (blue). ( G ) Pearson linear regression analysis of RUNX2 and Pan Ka fluorescence intensity. PDLSCs: periodontal ligament stem cells; Kla: lysine lactylation; PA: proanthocyanidins; Theo-24: theophylline (Data are expressed as mean ± SD, N = 3. * p < 0.05, ** p < 0.01, *** p < 0.001, NS indicates no statistical difference).

    Article Snippet: Primary antibodies are as follows: rabbit ant-IL-1β (1:1000, Cell Signaling Technology, Danvers, MA, USA); rabbit anti-coll I antibody (1:1000, ABclonal, Wuhan, China); rabbit anti-ALP antibody (1:1000, ABclonal, Wuhan, China); rabbit anti-RUNX2 antibody (1:1000, ABclonal, Wuhan, China); rabbit anti-BMP2 antibody (1:1000, ABclonal, Wuhan, China); and rabbit anti-Pan Kla antibody (1:1000, PTM Bio, Hangzhou, China).

    Techniques: Western Blot, Quantitative RT-PCR, Staining, Immunofluorescence, Expressing, Fluorescence

    Primer sequences.

    Journal: International Journal of Molecular Sciences

    Article Title: Proanthocyanidins Ameliorate LPS-Inhibited Osteogenesis of PDLSCs by Restoring Lysine Lactylation

    doi: 10.3390/ijms25052947

    Figure Lengend Snippet: Primer sequences.

    Article Snippet: Primary antibodies are as follows: rabbit ant-IL-1β (1:1000, Cell Signaling Technology, Danvers, MA, USA); rabbit anti-coll I antibody (1:1000, ABclonal, Wuhan, China); rabbit anti-ALP antibody (1:1000, ABclonal, Wuhan, China); rabbit anti-RUNX2 antibody (1:1000, ABclonal, Wuhan, China); rabbit anti-BMP2 antibody (1:1000, ABclonal, Wuhan, China); and rabbit anti-Pan Kla antibody (1:1000, PTM Bio, Hangzhou, China).

    Techniques: