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p130cas  (Santa Cruz Biotechnology)


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    Santa Cruz Biotechnology p130cas
    P130cas, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 202 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/p130cas/product/Santa Cruz Biotechnology
    Average 93 stars, based on 202 article reviews
    p130cas - by Bioz Stars, 2026-03
    93/100 stars

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    Figure 3. Time course of electret-induced <t>p130Cas</t> signaling. (A) Repre- sentative western blots of phospho-p130Cas, total p130Cas and GAPDH. (B) The graph shows increased p130Cas phosphorylation at residue Y410 in electret-stimulated cells (P-surface, white portion and N-surface, gray portion) compared with control cells (H-surface, black portion). *P < 0.05 vs. H-surface; data are the mean and standard deviation (n = 4).
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    Figure 3. Time course of electret-induced <t>p130Cas</t> signaling. (A) Repre- sentative western blots of phospho-p130Cas, total p130Cas and GAPDH. (B) The graph shows increased p130Cas phosphorylation at residue Y410 in electret-stimulated cells (P-surface, white portion and N-surface, gray portion) compared with control cells (H-surface, black portion). *P < 0.05 vs. H-surface; data are the mean and standard deviation (n = 4).
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    Figure 3. Time course of electret-induced p130Cas signaling. (A) Repre- sentative western blots of phospho-p130Cas, total p130Cas and GAPDH. (B) The graph shows increased p130Cas phosphorylation at residue Y410 in electret-stimulated cells (P-surface, white portion and N-surface, gray portion) compared with control cells (H-surface, black portion). *P < 0.05 vs. H-surface; data are the mean and standard deviation (n = 4).

    Journal: Journal of Hard Tissue Biology

    Article Title: Enhancement of Osteoblast Proliferation via ERK Signaling When Cultured on Electrically Polarized Hydroxyapatite

    doi: 10.2485/jhtb.34.93

    Figure Lengend Snippet: Figure 3. Time course of electret-induced p130Cas signaling. (A) Repre- sentative western blots of phospho-p130Cas, total p130Cas and GAPDH. (B) The graph shows increased p130Cas phosphorylation at residue Y410 in electret-stimulated cells (P-surface, white portion and N-surface, gray portion) compared with control cells (H-surface, black portion). *P < 0.05 vs. H-surface; data are the mean and standard deviation (n = 4).

    Article Snippet: Rabbit polyclonal phospho-p130Cas, phospho-ERK, phospho-p38 07[093-098]Takaaki Masutani_kk.indd 94 2025/04/02 9:10:12 95 MAPK, JNK antibodies, and rabbit monoclonal p130Cas, ERK, p38 MAPK, phospho-JNK antibodies were from Cell Signaling Technology (Denver, USA).

    Techniques: Western Blot, Phospho-proteomics, Residue, Control, Standard Deviation

    Figure 3. Time course of electret-induced p130Cas signaling. (A) Repre- sentative western blots of phospho-p130Cas, total p130Cas and GAPDH. (B) The graph shows increased p130Cas phosphorylation at residue Y410 in electret-stimulated cells (P-surface, white portion and N-surface, gray portion) compared with control cells (H-surface, black portion). *P < 0.05 vs. H-surface; data are the mean and standard deviation (n = 4).

    Journal: Journal of Hard Tissue Biology

    Article Title: Enhancement of Osteoblast Proliferation via ERK Signaling When Cultured on Electrically Polarized Hydroxyapatite

    doi: 10.2485/jhtb.34.93

    Figure Lengend Snippet: Figure 3. Time course of electret-induced p130Cas signaling. (A) Repre- sentative western blots of phospho-p130Cas, total p130Cas and GAPDH. (B) The graph shows increased p130Cas phosphorylation at residue Y410 in electret-stimulated cells (P-surface, white portion and N-surface, gray portion) compared with control cells (H-surface, black portion). *P < 0.05 vs. H-surface; data are the mean and standard deviation (n = 4).

    Article Snippet: Rabbit polyclonal phospho-p130Cas, phospho-ERK, phospho-p38 07[093-098]Takaaki Masutani_kk.indd 94 2025/04/02 9:10:12 95 MAPK, JNK antibodies, and rabbit monoclonal p130Cas, ERK, p38 MAPK, phospho-JNK antibodies were from Cell Signaling Technology (Denver, USA).

    Techniques: Western Blot, Phospho-proteomics, Residue, Control, Standard Deviation