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pakt ser 473 cell signaling technology  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc pakt ser 473 cell signaling technology
    Pakt Ser 473 Cell Signaling Technology, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 99/100, based on 32610 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pakt+(473)+antibody/Phospho-Akt+(Ser473)+Antibody/pmc12185721__41467_2025_60998_MOESM1_ESM-87-106-109
    Average 99 stars, based on 32610 article reviews
    pakt ser 473 cell signaling technology - by Bioz Stars, 2026-09
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    other:

    Article Title: Mechanical Ventilation With Moderate Tidal Volume Exacerbates Extrapulmonary Sepsis-Induced Lung Injury via IL33-WISP1 Signaling Pathway
    Article Snippet: IL-33 and WNT1-inducible secreted protein (WISP1) play central roles in acute lung injury (ALI) induced by mechanical ventilation with moderate tidal volume (MTV) in the setting of sepsis.. Here, we sought to determine the interrelationship between IL-33 and WISP1 and the associated signaling pathways in this process.. We used a two-hit model of cecal ligation puncture (CLP) followed by MTV ventilation (4 h 10 mL/kg) in wild-type, IL-33 / or ST2 / mice or wild-type mice treated with intratracheal antibodies to WISP1.



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    Figure 5. Differences in the activation of MAP kinases and AKT in response to PDGF-BB stimulation between pig arterial smooth muscle cells (ApSMCs) and venous smooth muscle cells (VpSMCs). (A,E) Confluent cells were serum-starved overnight and stimulated with PDGF-BB at the indicated time points. Cell lysates were analyzed for the expression of the indicated proteins via immunoblots. (B–D,F) Individual band densitometry data were obtained using Image J (NIH version 1.53K). The ratio values were obtained by dividing the band densitometry values of pERK1/2 (B), pJNK (C), pP38 (D) and <t>pAKT</t> (F) by the loading protein values (n = 4 for pERK1/2 and pJNK; n = 3 for pP38; n = 5 for pAKT). ****: p < 0.0001; ***: p < 0.001; **: p < 0.01; *: p < 0.05; ns: non-significant differences were assessed using an ANOVA test.
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    Figure 5. Differences in the activation of MAP kinases and AKT in response to PDGF-BB stimulation between pig arterial smooth muscle cells (ApSMCs) and venous smooth muscle cells (VpSMCs). (A,E) Confluent cells were serum-starved overnight and stimulated with PDGF-BB at the indicated time points. Cell lysates were analyzed for the expression of the indicated proteins via immunoblots. (B–D,F) Individual band densitometry data were obtained using Image J (NIH version 1.53K). The ratio values were obtained by dividing the band densitometry values of pERK1/2 (B), pJNK (C), pP38 (D) and <t>pAKT</t> (F) by the loading protein values (n = 4 for pERK1/2 and pJNK; n = 3 for pP38; n = 5 for pAKT). ****: p < 0.0001; ***: p < 0.001; **: p < 0.01; *: p < 0.05; ns: non-significant differences were assessed using an ANOVA test.
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    Figure 5. Differences in the activation of MAP kinases and AKT in response to PDGF-BB stimulation between pig arterial smooth muscle cells (ApSMCs) and venous smooth muscle cells (VpSMCs). (A,E) Confluent cells were serum-starved overnight and stimulated with PDGF-BB at the indicated time points. Cell lysates were analyzed for the expression of the indicated proteins via immunoblots. (B–D,F) Individual band densitometry data were obtained using Image J (NIH version 1.53K). The ratio values were obtained by dividing the band densitometry values of pERK1/2 (B), pJNK (C), pP38 (D) and pAKT (F) by the loading protein values (n = 4 for pERK1/2 and pJNK; n = 3 for pP38; n = 5 for pAKT). ****: p < 0.0001; ***: p < 0.001; **: p < 0.01; *: p < 0.05; ns: non-significant differences were assessed using an ANOVA test.

    Journal: International journal of molecular sciences

    Article Title: Characterization of Protein Expression and Signaling Pathway Activation That May Contribute to Differential Biological Functions in Porcine Arterial and Venous Smooth Muscle Cells.

    doi: 10.3390/ijms26073110

    Figure Lengend Snippet: Figure 5. Differences in the activation of MAP kinases and AKT in response to PDGF-BB stimulation between pig arterial smooth muscle cells (ApSMCs) and venous smooth muscle cells (VpSMCs). (A,E) Confluent cells were serum-starved overnight and stimulated with PDGF-BB at the indicated time points. Cell lysates were analyzed for the expression of the indicated proteins via immunoblots. (B–D,F) Individual band densitometry data were obtained using Image J (NIH version 1.53K). The ratio values were obtained by dividing the band densitometry values of pERK1/2 (B), pJNK (C), pP38 (D) and pAKT (F) by the loading protein values (n = 4 for pERK1/2 and pJNK; n = 3 for pP38; n = 5 for pAKT). ****: p < 0.0001; ***: p < 0.001; **: p < 0.01; *: p < 0.05; ns: non-significant differences were assessed using an ANOVA test.

    Article Snippet: The anti-ILK (3862), anti-TIMP-2 (5738), anti-pERK1/2(9101), anti-pJNK (9251), anti-pP38 (9211) and anti-pAKT (Serine 473) (9271) antibodies were purchased from Cell Signaling Technology, Inc. (Danvers, MA, USA).

    Techniques: Activation Assay, Expressing, Western Blot