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mouse monoclonal anti p21  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc mouse monoclonal anti p21
    Mouse Monoclonal Anti P21, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 600 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+monoclonal+anti+p21/pmc12887411-266-101-108?v=Cell+Signaling+Technology+Inc
    Average 96 stars, based on 600 article reviews
    mouse monoclonal anti p21 - by Bioz Stars, 2026-07
    96/100 stars

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    Effects of chlorogenic acid on cell cycle checkpoint pathways. Here, 3T3-L1 adipocytes were treated with H 2 O 2 (100 μM) on days 5, 6, and 7 of the differentiation process for three hours, followed by CGA exposure (5, 10, or 20 μM). Cells cultured with the differentiation medium containing the CGA vehicle alone (0.1% v / v DMSO) were used as controls. ( A , B ) Phospho-p53, <t>p21,</t> phosphorylated p38, and pERK1/2 protein expression was analyzed by Western blot. The densitometry results are reported as fold changes compared to control cells. The values were normalized to the corresponding β-actin value. All results are reported as the mean ± S.D. of three independent experiments (n = 3 biological replicates). Error bars represent S.D. a p < 0.01 vs. control cells; b p < 0.05 vs. control cells; c p < 0.05 vs. H 2 O 2 ; d p < 0.01 vs. H 2 O 2 ; e p < 0.01 vs. H 2 O 2 + CGA 5 μM; f p < 0.01 vs. H 2 O 2 + CGA 10 μM; g p < 0.05 vs. H 2 O 2 + CGA 5 μM.
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    Effects of chlorogenic acid on cell cycle checkpoint pathways. Here, 3T3-L1 adipocytes were treated with H 2 O 2 (100 μM) on days 5, 6, and 7 of the differentiation process for three hours, followed by CGA exposure (5, 10, or 20 μM). Cells cultured with the differentiation medium containing the CGA vehicle alone (0.1% v / v DMSO) were used as controls. ( A , B ) Phospho-p53, <t>p21,</t> phosphorylated p38, and pERK1/2 protein expression was analyzed by Western blot. The densitometry results are reported as fold changes compared to control cells. The values were normalized to the corresponding β-actin value. All results are reported as the mean ± S.D. of three independent experiments (n = 3 biological replicates). Error bars represent S.D. a p < 0.01 vs. control cells; b p < 0.05 vs. control cells; c p < 0.05 vs. H 2 O 2 ; d p < 0.01 vs. H 2 O 2 ; e p < 0.01 vs. H 2 O 2 + CGA 5 μM; f p < 0.01 vs. H 2 O 2 + CGA 10 μM; g p < 0.05 vs. H 2 O 2 + CGA 5 μM.
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    Cell Signaling Technology Inc monoclonal antibodies against p21 waf1 cip1
    Effects of chlorogenic acid on cell cycle checkpoint pathways. Here, 3T3-L1 adipocytes were treated with H 2 O 2 (100 μM) on days 5, 6, and 7 of the differentiation process for three hours, followed by CGA exposure (5, 10, or 20 μM). Cells cultured with the differentiation medium containing the CGA vehicle alone (0.1% v / v DMSO) were used as controls. ( A , B ) Phospho-p53, <t>p21,</t> phosphorylated p38, and pERK1/2 protein expression was analyzed by Western blot. The densitometry results are reported as fold changes compared to control cells. The values were normalized to the corresponding β-actin value. All results are reported as the mean ± S.D. of three independent experiments (n = 3 biological replicates). Error bars represent S.D. a p < 0.01 vs. control cells; b p < 0.05 vs. control cells; c p < 0.05 vs. H 2 O 2 ; d p < 0.01 vs. H 2 O 2 ; e p < 0.01 vs. H 2 O 2 + CGA 5 μM; f p < 0.01 vs. H 2 O 2 + CGA 10 μM; g p < 0.05 vs. H 2 O 2 + CGA 5 μM.
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    Effects of chlorogenic acid on cell cycle checkpoint pathways. Here, 3T3-L1 adipocytes were treated with H 2 O 2 (100 μM) on days 5, 6, and 7 of the differentiation process for three hours, followed by CGA exposure (5, 10, or 20 μM). Cells cultured with the differentiation medium containing the CGA vehicle alone (0.1% v / v DMSO) were used as controls. ( A , B ) Phospho-p53, <t>p21,</t> phosphorylated p38, and pERK1/2 protein expression was analyzed by Western blot. The densitometry results are reported as fold changes compared to control cells. The values were normalized to the corresponding β-actin value. All results are reported as the mean ± S.D. of three independent experiments (n = 3 biological replicates). Error bars represent S.D. a p < 0.01 vs. control cells; b p < 0.05 vs. control cells; c p < 0.05 vs. H 2 O 2 ; d p < 0.01 vs. H 2 O 2 ; e p < 0.01 vs. H 2 O 2 + CGA 5 μM; f p < 0.01 vs. H 2 O 2 + CGA 10 μM; g p < 0.05 vs. H 2 O 2 + CGA 5 μM.
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    Effects of chlorogenic acid on cell cycle checkpoint pathways. Here, 3T3-L1 adipocytes were treated with H 2 O 2 (100 μM) on days 5, 6, and 7 of the differentiation process for three hours, followed by CGA exposure (5, 10, or 20 μM). Cells cultured with the differentiation medium containing the CGA vehicle alone (0.1% v / v DMSO) were used as controls. ( A , B ) Phospho-p53, p21, phosphorylated p38, and pERK1/2 protein expression was analyzed by Western blot. The densitometry results are reported as fold changes compared to control cells. The values were normalized to the corresponding β-actin value. All results are reported as the mean ± S.D. of three independent experiments (n = 3 biological replicates). Error bars represent S.D. a p < 0.01 vs. control cells; b p < 0.05 vs. control cells; c p < 0.05 vs. H 2 O 2 ; d p < 0.01 vs. H 2 O 2 ; e p < 0.01 vs. H 2 O 2 + CGA 5 μM; f p < 0.01 vs. H 2 O 2 + CGA 10 μM; g p < 0.05 vs. H 2 O 2 + CGA 5 μM.

    Journal: Molecules

    Article Title: Effects of Chlorogenic Acid on Cellular Senescence in an In Vitro Model of 3T3-L1 Murine Adipocytes

    doi: 10.3390/molecules31010167

    Figure Lengend Snippet: Effects of chlorogenic acid on cell cycle checkpoint pathways. Here, 3T3-L1 adipocytes were treated with H 2 O 2 (100 μM) on days 5, 6, and 7 of the differentiation process for three hours, followed by CGA exposure (5, 10, or 20 μM). Cells cultured with the differentiation medium containing the CGA vehicle alone (0.1% v / v DMSO) were used as controls. ( A , B ) Phospho-p53, p21, phosphorylated p38, and pERK1/2 protein expression was analyzed by Western blot. The densitometry results are reported as fold changes compared to control cells. The values were normalized to the corresponding β-actin value. All results are reported as the mean ± S.D. of three independent experiments (n = 3 biological replicates). Error bars represent S.D. a p < 0.01 vs. control cells; b p < 0.05 vs. control cells; c p < 0.05 vs. H 2 O 2 ; d p < 0.01 vs. H 2 O 2 ; e p < 0.01 vs. H 2 O 2 + CGA 5 μM; f p < 0.01 vs. H 2 O 2 + CGA 10 μM; g p < 0.05 vs. H 2 O 2 + CGA 5 μM.

    Article Snippet: Membranes were then blocked using 5% non-fat dry milk solution and incubated overnight at 4 °C with the following specific primary antibodies: rabbit anti-Lamin B1 monoclonal antibody (Cell Signaling Technology, Danvers, MA, USA) (1:1000), mouse anti-PPAR-γ monoclonal antibody (Santa Cruz Biotechnology, Dallas, TX, USA) (1:1500), rabbit anti-PI3K p85 monoclonal antibody (Cell Signaling Technology) (1:1000), mouse anti-p21 (Waf1/Cip1) monoclonal antibody (Santa Cruz Biotechnology) (1:500), mouse anti-phospho-p53 (Ser15) monoclonal antibody (Cell Signaling Technology) (1:1000), rabbit anti-phospho-p38 (Thr180/Tyr182) monoclonal antibody (Cell Signaling Technology) (1:1000), rabbit anti-phospho-ERK1/2 (Thr202/Tyr204) monoclonal antibody (Cell Signaling Technology) (1:1000), rabbit anti-Bax monoclonal antibody (Cell Signaling Technology) (1:1000), rabbit anti-Bcl-2 monoclonal antibody (Cell Signaling Technology) (1:1000), rabbit anti-Phospho-Akt (Ser473) monoclonal antibody (Cell Signaling Technology) (1:1000), rabbit anti-GLUT-4 monoclonal antibody (Cell Signaling Technology) (1:1000), rabbit anti-NF-κB p65 polyclonal antibody (Invitrogen, Milan, Italy) (1:1000), mouse anti-COX-2 monoclonal antibody (Santa Cruz Biotechnology) (1:500), and rabbit anti-β-actin monoclonal antibody (Cell Signaling Technology) (1:6000).

    Techniques: Cell Culture, Expressing, Western Blot, Control