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p foxo3a ser318 321 mab  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc p foxo3a ser318 321 mab
    P Foxo3a Ser318 321 Mab, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 168 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 95 stars, based on 168 article reviews
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    other:

    Article Title: Insulin receptor substrate signaling suppresses neonatal autophagy in the heart
    Article Snippet: Primary antibodies against ACC, AKT, AMPKα, Atg7, BECN1, BCL2, caspase-8, cleaved caspase-9, caspase-12, cleaved PARP Asp214 , FoxO1, GAPDH, mTOR, P-ACC Ser79 , P-AKT Ser473 , P-AKT Thr308 , P-AMPKα Thr172 , P-FoxO1 Thr24 /FoxO3a Thr32 , P-FoxO3a Ser318/321 , P-mTOR Ser2448 , P-S6 ribosomal protein Ser235/236 , P-ULK1 Ser555 , P-ULK1 Ser757 , and S6 ribosomal protein were from Cell Signaling.



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    Effects of Agastache rugosa extract (ARE) and tilianin on protein-degradation-related pathways in C2C12 myotubes. C2C12 myotubes were simultaneously exposed to tumor necrosis factor-α (TNF-α, 50 ng/mL) along with ARE (40 and 80 μg/mL) or tilianin (20 and 40 μM). Western blot analysis was used to assess the protein expression levels of phosphorylated-forkhead box class O 3 (p-FoxO3) and FoxO3 in response to (A) ARE and (B) tilianin. α-Tubulin served as the internal control. Reverse transcription polymerase chain reaction was used to determine the mRNA expression levels of muscle RING-finger protein-1 (MuRF1) and atrogin-1 in response to (C) ARE and (D) tilianin. β-Actin served as the internal control. Experimental results were presented as the mean±SD. Significant differences were assessed using Duncan’s multiple range test. # P <0.05, ## P <0.01 (control group vs. TNF-α group); * P <0.05, ** P <0.01 (TNF-α group vs. ARE or tilianin group).

    Journal: Preventive Nutrition and Food Science

    Article Title: Korean Mint ( Agastache rugosa ) Extract and Its Bioactive Compound Tilianin Alleviate Muscle Atrophy via the PI3K/Akt/FoxO3 Pathway in C2C12 Myotubes

    doi: 10.3746/pnf.2024.29.2.154

    Figure Lengend Snippet: Effects of Agastache rugosa extract (ARE) and tilianin on protein-degradation-related pathways in C2C12 myotubes. C2C12 myotubes were simultaneously exposed to tumor necrosis factor-α (TNF-α, 50 ng/mL) along with ARE (40 and 80 μg/mL) or tilianin (20 and 40 μM). Western blot analysis was used to assess the protein expression levels of phosphorylated-forkhead box class O 3 (p-FoxO3) and FoxO3 in response to (A) ARE and (B) tilianin. α-Tubulin served as the internal control. Reverse transcription polymerase chain reaction was used to determine the mRNA expression levels of muscle RING-finger protein-1 (MuRF1) and atrogin-1 in response to (C) ARE and (D) tilianin. β-Actin served as the internal control. Experimental results were presented as the mean±SD. Significant differences were assessed using Duncan’s multiple range test. # P <0.05, ## P <0.01 (control group vs. TNF-α group); * P <0.05, ** P <0.01 (TNF-α group vs. ARE or tilianin group).

    Article Snippet: Next, the membrane was incubated overnight at 4°C with the primary antibodies against α-tubulin, NF-κB (Santa Cruz Biotechnology Inc.), PI3K, phosphorylated-PI3K (p-PI3K), Akt, phosphorylated-Akt (p-Akt), 70-kDa ribosomal protein S6 kinase (p70S6K), phosphorylated-p70S6K (p-p70S6K), eukaryotic initiation factor 4E binding protein 1 (4EBP1), phosphorylated-4EBP1 (p-4EBP1), mTOR, phosphorylated-mTOR (p-mTOR), FoxO3, and phosphorylated-FoxO3 (p-FoxO3) (Cell Signaling Technology).

    Techniques: Western Blot, Expressing, Control, Reverse Transcription, Polymerase Chain Reaction