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ab32047 rrid ab 722764 rabbit anti sesn2 proteintech cat 10795 1 ap rrid ab 2185480 rabbit phospho p44 42 mapk  (Proteintech)


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    Proteintech ab32047 rrid ab 722764 rabbit anti sesn2 proteintech cat 10795 1 ap rrid ab 2185480 rabbit phospho p44 42 mapk
    Ab32047 Rrid Ab 722764 Rabbit Anti Sesn2 Proteintech Cat 10795 1 Ap Rrid Ab 2185480 Rabbit Phospho P44 42 Mapk, supplied by Proteintech, used in various techniques. Bioz Stars score: 95/100, based on 147 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ab32047 rrid ab 722764 rabbit anti sesn2 proteintech cat 10795 1 ap rrid ab 2185480 rabbit phospho p44 42 mapk/product/Proteintech
    Average 95 stars, based on 147 article reviews
    ab32047 rrid ab 722764 rabbit anti sesn2 proteintech cat 10795 1 ap rrid ab 2185480 rabbit phospho p44 42 mapk - by Bioz Stars, 2026-03
    95/100 stars

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    Aldoa promotes osteogenesis and angiogenesis via the ERK/Hif-1α pathway. A, Alizarin red staining (14 days) and ALP staining (7 days). B, The gene expression levels of Runx2, Alp and Ocn were determined by qRT-PCR. β-actin was used as an internal reference gene. C, Tube formation assay was performed in the presence of CM. The scale bars represent 100 μm. D, The mRNA expression levels of Vegf and CD31 were analysed by quantitative RT-PCR. β-actin was used as an internal reference gene. E, Immunofluorescence staining was performed to detect Vegf expression after being treated by CM. The scale bars represent 25 μm. F, A Kyoto Encyclopaedia of Genes and Genomes (KEGG) enrichment analysis was performed to determine the top related pathways involving these differentially expressed mRNAs. G and H, The protein expression levels of Aldoa, Hif-1α and the phosphorylated of ERK, JUK and <t>p38</t> among hypoxia, normoxia and hypoxia + si-Aldoa groups were determined by western blot. Semiquantitative analysis of the p-ERK/ERK, p-JUK/JUK and p38/p-p38 ratios were shown. β-actin was used as an internal reference gene. All data were expressed as means ± SD. * P < .05, ** P < .01.
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    Aldoa promotes osteogenesis and angiogenesis via the ERK/Hif-1α pathway. A, Alizarin red staining (14 days) and ALP staining (7 days). B, The gene expression levels of Runx2, Alp and Ocn were determined by qRT-PCR. β-actin was used as an internal reference gene. C, Tube formation assay was performed in the presence of CM. The scale bars represent 100 μm. D, The mRNA expression levels of Vegf and CD31 were analysed by quantitative RT-PCR. β-actin was used as an internal reference gene. E, Immunofluorescence staining was performed to detect Vegf expression after being treated by CM. The scale bars represent 25 μm. F, A Kyoto Encyclopaedia of Genes and Genomes (KEGG) enrichment analysis was performed to determine the top related pathways involving these differentially expressed mRNAs. G and H, The protein expression levels of Aldoa, Hif-1α and the phosphorylated of ERK, JUK and <t>p38</t> among hypoxia, normoxia and hypoxia + si-Aldoa groups were determined by western blot. Semiquantitative analysis of the p-ERK/ERK, p-JUK/JUK and p38/p-p38 ratios were shown. β-actin was used as an internal reference gene. All data were expressed as means ± SD. * P < .05, ** P < .01.
    Ab32047 Rrid Ab 722764 Rabbit Anti Sesn2 Proteintech Cat 10795 1 Ap Rrid Ab 2185480 Rabbit Phospho P44 42 Mapk, supplied by Proteintech, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Aldoa promotes osteogenesis and angiogenesis via the ERK/Hif-1α pathway. A, Alizarin red staining (14 days) and ALP staining (7 days). B, The gene expression levels of Runx2, Alp and Ocn were determined by qRT-PCR. β-actin was used as an internal reference gene. C, Tube formation assay was performed in the presence of CM. The scale bars represent 100 μm. D, The mRNA expression levels of Vegf and CD31 were analysed by quantitative RT-PCR. β-actin was used as an internal reference gene. E, Immunofluorescence staining was performed to detect Vegf expression after being treated by CM. The scale bars represent 25 μm. F, A Kyoto Encyclopaedia of Genes and Genomes (KEGG) enrichment analysis was performed to determine the top related pathways involving these differentially expressed mRNAs. G and H, The protein expression levels of Aldoa, Hif-1α and the phosphorylated of ERK, JUK and <t>p38</t> among hypoxia, normoxia and hypoxia + si-Aldoa groups were determined by western blot. Semiquantitative analysis of the p-ERK/ERK, p-JUK/JUK and p38/p-p38 ratios were shown. β-actin was used as an internal reference gene. All data were expressed as means ± SD. * P < .05, ** P < .01.
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    Aldoa promotes osteogenesis and angiogenesis via the ERK/Hif-1α pathway. A, Alizarin red staining (14 days) and ALP staining (7 days). B, The gene expression levels of Runx2, Alp and Ocn were determined by qRT-PCR. β-actin was used as an internal reference gene. C, Tube formation assay was performed in the presence of CM. The scale bars represent 100 μm. D, The mRNA expression levels of Vegf and CD31 were analysed by quantitative RT-PCR. β-actin was used as an internal reference gene. E, Immunofluorescence staining was performed to detect Vegf expression after being treated by CM. The scale bars represent 25 μm. F, A Kyoto Encyclopaedia of Genes and Genomes (KEGG) enrichment analysis was performed to determine the top related pathways involving these differentially expressed mRNAs. G and H, The protein expression levels of Aldoa, Hif-1α and the phosphorylated of ERK, JUK and <t>p38</t> among hypoxia, normoxia and hypoxia + si-Aldoa groups were determined by western blot. Semiquantitative analysis of the p-ERK/ERK, p-JUK/JUK and p38/p-p38 ratios were shown. β-actin was used as an internal reference gene. All data were expressed as means ± SD. * P < .05, ** P < .01.
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    Aldoa promotes osteogenesis and angiogenesis via the ERK/Hif-1α pathway. A, Alizarin red staining (14 days) and ALP staining (7 days). B, The gene expression levels of Runx2, Alp and Ocn were determined by qRT-PCR. β-actin was used as an internal reference gene. C, Tube formation assay was performed in the presence of CM. The scale bars represent 100 μm. D, The mRNA expression levels of Vegf and CD31 were analysed by quantitative RT-PCR. β-actin was used as an internal reference gene. E, Immunofluorescence staining was performed to detect Vegf expression after being treated by CM. The scale bars represent 25 μm. F, A Kyoto Encyclopaedia of Genes and Genomes (KEGG) enrichment analysis was performed to determine the top related pathways involving these differentially expressed mRNAs. G and H, The protein expression levels of Aldoa, Hif-1α and the phosphorylated of ERK, JUK and <t>p38</t> among hypoxia, normoxia and hypoxia + si-Aldoa groups were determined by western blot. Semiquantitative analysis of the p-ERK/ERK, p-JUK/JUK and p38/p-p38 ratios were shown. β-actin was used as an internal reference gene. All data were expressed as means ± SD. * P < .05, ** P < .01.
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    Aldoa promotes osteogenesis and angiogenesis via the ERK/Hif-1α pathway. A, Alizarin red staining (14 days) and ALP staining (7 days). B, The gene expression levels of Runx2, Alp and Ocn were determined by qRT-PCR. β-actin was used as an internal reference gene. C, Tube formation assay was performed in the presence of CM. The scale bars represent 100 μm. D, The mRNA expression levels of Vegf and CD31 were analysed by quantitative RT-PCR. β-actin was used as an internal reference gene. E, Immunofluorescence staining was performed to detect Vegf expression after being treated by CM. The scale bars represent 25 μm. F, A Kyoto Encyclopaedia of Genes and Genomes (KEGG) enrichment analysis was performed to determine the top related pathways involving these differentially expressed mRNAs. G and H, The protein expression levels of Aldoa, Hif-1α and the phosphorylated of ERK, JUK and <t>p38</t> among hypoxia, normoxia and hypoxia + si-Aldoa groups were determined by western blot. Semiquantitative analysis of the p-ERK/ERK, p-JUK/JUK and p38/p-p38 ratios were shown. β-actin was used as an internal reference gene. All data were expressed as means ± SD. * P < .05, ** P < .01.
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    (A) Representative immunofluorescence-staining images of phosphorylated <t>p38-MAPK</t> expression in scar tissue at week 0, week 2, and week 6 post-treatments. Scale bar = 200 or 50 μm. (B) ROS activity in scar tissue at week 0, week 2, and week 6 post-treatments. (C) Quantitative evaluation of phosphorylated p38-MAPK expression in scar tissue. Notes: compared with normal skin (NS), ** P < 0.01, *** P < 0.001,**** P < 0.0001; compared with NC, △△ P < 0.01, △△△△ P < 0.0001; compared with MSN@Res, #### P < 0.0001.
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    Cell Signaling Technology Inc rabbit polyclonal phospho-p44/42 mapk antibody (erk1/2)
    (A) Representative immunofluorescence-staining images of phosphorylated <t>p38-MAPK</t> expression in scar tissue at week 0, week 2, and week 6 post-treatments. Scale bar = 200 or 50 μm. (B) ROS activity in scar tissue at week 0, week 2, and week 6 post-treatments. (C) Quantitative evaluation of phosphorylated p38-MAPK expression in scar tissue. Notes: compared with normal skin (NS), ** P < 0.01, *** P < 0.001,**** P < 0.0001; compared with NC, △△ P < 0.01, △△△△ P < 0.0001; compared with MSN@Res, #### P < 0.0001.
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    Image Search Results


    Aldoa promotes osteogenesis and angiogenesis via the ERK/Hif-1α pathway. A, Alizarin red staining (14 days) and ALP staining (7 days). B, The gene expression levels of Runx2, Alp and Ocn were determined by qRT-PCR. β-actin was used as an internal reference gene. C, Tube formation assay was performed in the presence of CM. The scale bars represent 100 μm. D, The mRNA expression levels of Vegf and CD31 were analysed by quantitative RT-PCR. β-actin was used as an internal reference gene. E, Immunofluorescence staining was performed to detect Vegf expression after being treated by CM. The scale bars represent 25 μm. F, A Kyoto Encyclopaedia of Genes and Genomes (KEGG) enrichment analysis was performed to determine the top related pathways involving these differentially expressed mRNAs. G and H, The protein expression levels of Aldoa, Hif-1α and the phosphorylated of ERK, JUK and p38 among hypoxia, normoxia and hypoxia + si-Aldoa groups were determined by western blot. Semiquantitative analysis of the p-ERK/ERK, p-JUK/JUK and p38/p-p38 ratios were shown. β-actin was used as an internal reference gene. All data were expressed as means ± SD. * P < .05, ** P < .01.

    Journal: International Dental Journal

    Article Title: 4632427E13Rik Facilitates Jaw Marrow-Derived Mesenchymal Stem Cells Osteogenesis and Angiogenesis Under Hypoxia Through miR-34a-5p/Aldoa/Hif-1α Pathway

    doi: 10.1016/j.identj.2025.109364

    Figure Lengend Snippet: Aldoa promotes osteogenesis and angiogenesis via the ERK/Hif-1α pathway. A, Alizarin red staining (14 days) and ALP staining (7 days). B, The gene expression levels of Runx2, Alp and Ocn were determined by qRT-PCR. β-actin was used as an internal reference gene. C, Tube formation assay was performed in the presence of CM. The scale bars represent 100 μm. D, The mRNA expression levels of Vegf and CD31 were analysed by quantitative RT-PCR. β-actin was used as an internal reference gene. E, Immunofluorescence staining was performed to detect Vegf expression after being treated by CM. The scale bars represent 25 μm. F, A Kyoto Encyclopaedia of Genes and Genomes (KEGG) enrichment analysis was performed to determine the top related pathways involving these differentially expressed mRNAs. G and H, The protein expression levels of Aldoa, Hif-1α and the phosphorylated of ERK, JUK and p38 among hypoxia, normoxia and hypoxia + si-Aldoa groups were determined by western blot. Semiquantitative analysis of the p-ERK/ERK, p-JUK/JUK and p38/p-p38 ratios were shown. β-actin was used as an internal reference gene. All data were expressed as means ± SD. * P < .05, ** P < .01.

    Article Snippet: Rabbit anti-Aldoa (1:1000, 11217-1-AP), rabbit anti-Hif-1α (1:1000, ab179483), rabbit anti-Runx2 (1:1000, 8486S), rabbit anti-CD31 (1:1000, 77699S), rabbit anti-Ocn (1:1000, bs-4917R), rabbit anti-Alp (1:1000, bs-1535R), rabbit anti-Vegf (1:1000, bs-1313R), rabbit anti-ERK (1:1000, bsm-33337M), rabbit anti-p-ERK (1:1000, bs-1646R), rabbit anti-p38 (1:1000, bs-0637R), rabbit anti-p-p38 (1:1000, bs-0636R), rabbit anti-JNK (1:1000, bs-2592R), rabbit anti-p-JNK (1:1000, bs-1640R), and mouse anti-β-actin (1:2000, AF7018) were purchased from Proteintech, Abcam, Cell Signalling Technology, and Bioss, respectively.

    Techniques: Staining, Gene Expression, Quantitative RT-PCR, Tube Formation Assay, Expressing, Immunofluorescence, Western Blot

    (A) Representative immunofluorescence-staining images of phosphorylated p38-MAPK expression in scar tissue at week 0, week 2, and week 6 post-treatments. Scale bar = 200 or 50 μm. (B) ROS activity in scar tissue at week 0, week 2, and week 6 post-treatments. (C) Quantitative evaluation of phosphorylated p38-MAPK expression in scar tissue. Notes: compared with normal skin (NS), ** P < 0.01, *** P < 0.001,**** P < 0.0001; compared with NC, △△ P < 0.01, △△△△ P < 0.0001; compared with MSN@Res, #### P < 0.0001.

    Journal: ACS Omega

    Article Title: Injectable Thermosensitive Hydrogel Containing Resveratrol-Laden Nanoparticles Promotes Hypertrophic Scar Repair in Rat Tail

    doi: 10.1021/acsomega.5c01469

    Figure Lengend Snippet: (A) Representative immunofluorescence-staining images of phosphorylated p38-MAPK expression in scar tissue at week 0, week 2, and week 6 post-treatments. Scale bar = 200 or 50 μm. (B) ROS activity in scar tissue at week 0, week 2, and week 6 post-treatments. (C) Quantitative evaluation of phosphorylated p38-MAPK expression in scar tissue. Notes: compared with normal skin (NS), ** P < 0.01, *** P < 0.001,**** P < 0.0001; compared with NC, △△ P < 0.01, △△△△ P < 0.0001; compared with MSN@Res, #### P < 0.0001.

    Article Snippet: Subsequently, they were kept at 4 °C overnight in the presence of rabbit antiphosphorylated p38-MAPK (p-p38, bs-5476R, Bioss, China, 1:400), rabbit anti-LC3-II (LC3-II, 14600–1-AP, Aspen, China, 1:500), rabbit anti-cleaved caspase-3 (Cleaved Caspase 3, 25128–1-AP, Aspen, China, 1:150), rodent-derived p53 antibody (p53, 60283–2-IG, Aspen, China, 1:400), and a rat-originated HIF-1α antibody (HIF-1α, SC-13515, Santa Cruz, 1:100).

    Techniques: Immunofluorescence, Staining, Expressing, Activity Assay