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mouse monoclonal anti phospho akt ser473  (Proteintech)


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    Structured Review

    Proteintech mouse monoclonal anti phospho akt ser473
    Mouse Monoclonal Anti Phospho Akt Ser473, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 2134 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/akt+mouse+monoclonal+antibody/Phospho-AKT+(Ser473)+Antibody/pmc13031519-46-15-20
    Average 96 stars, based on 2134 article reviews
    mouse monoclonal anti phospho akt ser473 - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    other:

    Article Title: Celastrol inhibits the proliferation and migration of MCF-7 cells through the leptin-triggered PI3K/AKT pathway.
    Article Snippet: AKT Mouse Monoclonal Antibody (cat number: 10176-2-AP) and LEPR Antibody (cat number: 20996-1-AP) were obtained from Proteintech, Phospho-AKT (Ser473) Antibody (cat number: 9271), PI3 Kinase p85 Antibody (cat number: 4257), mTOR Antibody (cat number: 2983), Phospho-mTOR (Ser2481) Antibody (cat number: 2974) was obtained from Cell Signaling Technology, PhosphoPI3 Kinase p85 alpha (Tyr607) Antibody (cat number: AF 3241) was obtained from Affinity Biosciences.

    Article Title: Celastrol inhibits the proliferation and migration of MCF-7 cells through the leptin-triggered PI3K/AKT pathway
    Article Snippet: AKT Mouse Monoclonal Antibody (cat number: 10176-2-AP) and LEPR Antibody (cat number: 20996-1-AP) were obtained from Proteintech, Phospho-AKT (Ser473) Antibody (cat number: 9271), PI3 Kinase p85 Antibody (cat number: 4257), mTOR Antibody (cat number: 2983), Phospho-mTOR (Ser2481) Antibody (cat number: 2974) was obtained from Cell Signaling Technology, Phospho-PI3 Kinase p85 alpha (Tyr607) Antibody (cat number: AF −3241) was obtained from Affinity Biosciences.

    Blocking Assay:

    Article Title: Fabrication of high-strength mecobalamin loaded aligned silk fibroin scaffolds for guiding neuronal orientation.
    Article Snippet: Suitable micro/nanofibers orientation in tissue engineered scaffold could guide cells outgrowth and migration during tissue regeneration.. However, it is still a challenge to prepare a simple, high-strength and aligned fibers scaffold.. Herein, we report a facile strategy to construct high-strength silk fibroin (SF) scaffolds with aligned fibers orientation by crosslinking aligned SF fibers with regenerated SF solution for guiding neuronal growth direction.

    Membrane:

    Article Title: Fabrication of high-strength mecobalamin loaded aligned silk fibroin scaffolds for guiding neuronal orientation.
    Article Snippet: Suitable micro/nanofibers orientation in tissue engineered scaffold could guide cells outgrowth and migration during tissue regeneration.. However, it is still a challenge to prepare a simple, high-strength and aligned fibers scaffold.. Herein, we report a facile strategy to construct high-strength silk fibroin (SF) scaffolds with aligned fibers orientation by crosslinking aligned SF fibers with regenerated SF solution for guiding neuronal growth direction.

    Incubation:

    Article Title: Fabrication of high-strength mecobalamin loaded aligned silk fibroin scaffolds for guiding neuronal orientation.
    Article Snippet: Suitable micro/nanofibers orientation in tissue engineered scaffold could guide cells outgrowth and migration during tissue regeneration.. However, it is still a challenge to prepare a simple, high-strength and aligned fibers scaffold.. Herein, we report a facile strategy to construct high-strength silk fibroin (SF) scaffolds with aligned fibers orientation by crosslinking aligned SF fibers with regenerated SF solution for guiding neuronal growth direction.



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    Cell Signaling Technology Inc mouse monoclonal antibodies against phospho akt ser473
    Effect of circ-CCDC134 and linear-CCDC134 overexpression on the phosphorylation of AKT and STAT3. Jurkat cells were transfected with plasmid encoding circ-CCDC134, plasmid encoding linear CCDC134 and respective empty plasmid. Then the cells were further stimulated with PMA (20 ng/mL) and ionomycin (500 ng/mL) for 1 hour. A Overexpression of circ-CCDC134 increased AKT phosphorylation at Thr308. B Overexpression of circ-CCDC134 increased AKT phosphorylation at <t>Ser473.</t> C A representative example. D Overexpression of linear CCDC134 did not affect AKT phosphorylation at Thr308. E Overexpression of linear CCDC134 did not affect AKT phosphorylation at Ser473. F A representative example. G Overexpression of circ-CCDC134 increased STAT3 phosphorylation at Ser727. H Overexpression of circ-CCDC134 did not affect STAT3 phosphorylation at Tyr705. I A representative example. J Overexpression of linear CCDC134 did not affect STAT3 phosphorylation at Ser727. K Overexpression of linear CCDC134 did not affect STAT3 phosphorylation at Tyr705. L A representative example. (ns, not significant; * P < 0.05; ** P < 0.01; *** P < 0.001)
    Mouse Monoclonal Antibodies Against Phospho Akt Ser473, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Cell Signaling Technology Inc mouse monoclonal anti akt pan
    Effect of circ-CCDC134 and linear-CCDC134 overexpression on the phosphorylation of AKT and STAT3. Jurkat cells were transfected with plasmid encoding circ-CCDC134, plasmid encoding linear CCDC134 and respective empty plasmid. Then the cells were further stimulated with PMA (20 ng/mL) and ionomycin (500 ng/mL) for 1 hour. A Overexpression of circ-CCDC134 increased AKT phosphorylation at Thr308. B Overexpression of circ-CCDC134 increased AKT phosphorylation at <t>Ser473.</t> C A representative example. D Overexpression of linear CCDC134 did not affect AKT phosphorylation at Thr308. E Overexpression of linear CCDC134 did not affect AKT phosphorylation at Ser473. F A representative example. G Overexpression of circ-CCDC134 increased STAT3 phosphorylation at Ser727. H Overexpression of circ-CCDC134 did not affect STAT3 phosphorylation at Tyr705. I A representative example. J Overexpression of linear CCDC134 did not affect STAT3 phosphorylation at Ser727. K Overexpression of linear CCDC134 did not affect STAT3 phosphorylation at Tyr705. L A representative example. (ns, not significant; * P < 0.05; ** P < 0.01; *** P < 0.001)
    Mouse Monoclonal Anti Akt Pan, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/akt+mouse+monoclonal+antibody/Akt+(pan)+Mouse+mAb/pmc12949489-9-0-5
    Average 96 stars, based on 1 article reviews
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    Image Search Results


    Effect of circ-CCDC134 and linear-CCDC134 overexpression on the phosphorylation of AKT and STAT3. Jurkat cells were transfected with plasmid encoding circ-CCDC134, plasmid encoding linear CCDC134 and respective empty plasmid. Then the cells were further stimulated with PMA (20 ng/mL) and ionomycin (500 ng/mL) for 1 hour. A Overexpression of circ-CCDC134 increased AKT phosphorylation at Thr308. B Overexpression of circ-CCDC134 increased AKT phosphorylation at Ser473. C A representative example. D Overexpression of linear CCDC134 did not affect AKT phosphorylation at Thr308. E Overexpression of linear CCDC134 did not affect AKT phosphorylation at Ser473. F A representative example. G Overexpression of circ-CCDC134 increased STAT3 phosphorylation at Ser727. H Overexpression of circ-CCDC134 did not affect STAT3 phosphorylation at Tyr705. I A representative example. J Overexpression of linear CCDC134 did not affect STAT3 phosphorylation at Ser727. K Overexpression of linear CCDC134 did not affect STAT3 phosphorylation at Tyr705. L A representative example. (ns, not significant; * P < 0.05; ** P < 0.01; *** P < 0.001)

    Journal: Arthritis Research & Therapy

    Article Title: Decreased expression of circ-CCDC134 mediated by TNF-α in patients with rheumatoid arthritis affects T cell function via targeting protein phosphatase 2A

    doi: 10.1186/s13075-026-03763-4

    Figure Lengend Snippet: Effect of circ-CCDC134 and linear-CCDC134 overexpression on the phosphorylation of AKT and STAT3. Jurkat cells were transfected with plasmid encoding circ-CCDC134, plasmid encoding linear CCDC134 and respective empty plasmid. Then the cells were further stimulated with PMA (20 ng/mL) and ionomycin (500 ng/mL) for 1 hour. A Overexpression of circ-CCDC134 increased AKT phosphorylation at Thr308. B Overexpression of circ-CCDC134 increased AKT phosphorylation at Ser473. C A representative example. D Overexpression of linear CCDC134 did not affect AKT phosphorylation at Thr308. E Overexpression of linear CCDC134 did not affect AKT phosphorylation at Ser473. F A representative example. G Overexpression of circ-CCDC134 increased STAT3 phosphorylation at Ser727. H Overexpression of circ-CCDC134 did not affect STAT3 phosphorylation at Tyr705. I A representative example. J Overexpression of linear CCDC134 did not affect STAT3 phosphorylation at Ser727. K Overexpression of linear CCDC134 did not affect STAT3 phosphorylation at Tyr705. L A representative example. (ns, not significant; * P < 0.05; ** P < 0.01; *** P < 0.001)

    Article Snippet: The antibodies used for the Western blot analysis included rabbit monoclonal antibodies against Jun N-terminal kinases (JNK), phospho-JNK (Thr183/Tyr185), AKT, phospho-AKT (Thr308), Signal transducer and activator of transcription 3 (STAT3), phospho-STAT3 (Ser727), poly(rC)-binding protein 2 (PCBP2), the alpha isoform of protein phosphatase 2 A (PP2A) scaffold subunit A (PPP2R1A), in addition to mouse monoclonal antibodies against phospho-AKT (Ser473) and phospho-STAT3 (Tyr705) (Cell Signaling Technology, Danvers, MA, USA).

    Techniques: Over Expression, Phospho-proteomics, Transfection, Plasmid Preparation