phospho akt ser473 d9e xp rabbit mab  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phospho akt ser473 d9e xp rabbit mab
    Phospho Akt Ser473 D9e Xp Rabbit Mab, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    phospho akt ser473 d9e xp rabbit mab  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phospho akt ser473 d9e xp rabbit mab
    Phospho Akt Ser473 D9e Xp Rabbit Mab, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    phospho akt rabbit mab  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phospho akt rabbit mab
    The effect of aging <t>on</t> <t>IκBα</t> and <t>Akt</t> following hemorrhagic shock (trauma/hemorrhage, TH) and femoral fracture (Fx) in young (17-26 weeks) and aged (64-72 weeks) male C57BL/6J mice. The experimental design included young (17-26 weeks) and aged (64-72 weeks) C57BL/6J mice in both sham and trauma groups. The trauma groups underwent a pressure-controlled hemorrhagic shock and Fx (via osteotomy) (THFx), while the sham groups underwent catheterization and received an external fixator, but no THFx was induced. After twenty-four hours, the mice were euthanized, and sampling was performed. (A) Western blot analysis of phosphorylated and non-phosphorylated IκBα, AKT as well as β-Actin, and quantification of (B) the phosphorylation ratio of IκBα, and (C) AKT in liver tissue. n=4 in each group, *: p<0.05 between indicated groups.
    Phospho Akt Rabbit Mab, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/phospho akt rabbit mab/product/Cell Signaling Technology Inc
    Average 86 stars, based on 1 article reviews
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    Images

    1) Product Images from "Impact of age on liver damage, inflammation, and molecular signaling pathways in response to femoral fracture and hemorrhage"

    Article Title: Impact of age on liver damage, inflammation, and molecular signaling pathways in response to femoral fracture and hemorrhage

    Journal: Frontiers in Immunology

    doi: 10.3389/fimmu.2023.1239145

    The effect of aging on IκBα and Akt following hemorrhagic shock (trauma/hemorrhage, TH) and femoral fracture (Fx) in young (17-26 weeks) and aged (64-72 weeks) male C57BL/6J mice. The experimental design included young (17-26 weeks) and aged (64-72 weeks) C57BL/6J mice in both sham and trauma groups. The trauma groups underwent a pressure-controlled hemorrhagic shock and Fx (via osteotomy) (THFx), while the sham groups underwent catheterization and received an external fixator, but no THFx was induced. After twenty-four hours, the mice were euthanized, and sampling was performed. (A) Western blot analysis of phosphorylated and non-phosphorylated IκBα, AKT as well as β-Actin, and quantification of (B) the phosphorylation ratio of IκBα, and (C) AKT in liver tissue. n=4 in each group, *: p<0.05 between indicated groups.
    Figure Legend Snippet: The effect of aging on IκBα and Akt following hemorrhagic shock (trauma/hemorrhage, TH) and femoral fracture (Fx) in young (17-26 weeks) and aged (64-72 weeks) male C57BL/6J mice. The experimental design included young (17-26 weeks) and aged (64-72 weeks) C57BL/6J mice in both sham and trauma groups. The trauma groups underwent a pressure-controlled hemorrhagic shock and Fx (via osteotomy) (THFx), while the sham groups underwent catheterization and received an external fixator, but no THFx was induced. After twenty-four hours, the mice were euthanized, and sampling was performed. (A) Western blot analysis of phosphorylated and non-phosphorylated IκBα, AKT as well as β-Actin, and quantification of (B) the phosphorylation ratio of IκBα, and (C) AKT in liver tissue. n=4 in each group, *: p<0.05 between indicated groups.

    Techniques Used: Sampling, Western Blot

    rabbit monoclonal anti phospho akt ser473 igg  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit monoclonal anti phospho akt ser473 igg

    Rabbit Monoclonal Anti Phospho Akt Ser473 Igg, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Images

    1) Product Images from "mTORC2 regulates auditory hair cell structure and function"

    Article Title: mTORC2 regulates auditory hair cell structure and function

    Journal: iScience

    doi: 10.1016/j.isci.2023.107687


    Figure Legend Snippet:

    Techniques Used: Recombinant, Saline, Electron Microscopy, Software, Imaging

    anti phospho akt thr308 c31e5e rabbit mab  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc anti phospho akt thr308 c31e5e rabbit mab
    Anti Phospho Akt Thr308 C31e5e Rabbit Mab, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    rabbit monoclonal anti phospho akt substrate rxxs∗ t∗  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit monoclonal anti phospho akt substrate rxxs∗ t∗

    Rabbit Monoclonal Anti Phospho Akt Substrate Rxxs∗ T∗, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Activation of AKT induces EZH2-mediated β-catenin trimethylation in colorectal cancer"

    Article Title: Activation of AKT induces EZH2-mediated β-catenin trimethylation in colorectal cancer

    Journal: iScience

    doi: 10.1016/j.isci.2023.107630


    Figure Legend Snippet:

    Techniques Used: Virus, shRNA, Plasmid Preparation, Recombinant, Protease Inhibitor, DNA Purification, Mutagenesis, Software

    rabbit monoclonal anti phospho akt ser473  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit monoclonal anti phospho akt ser473

    Rabbit Monoclonal Anti Phospho Akt Ser473, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Activation of GPR44 decreases severity of myeloid leukemia via specific targeting of leukemia initiating stem cells"

    Article Title: Activation of GPR44 decreases severity of myeloid leukemia via specific targeting of leukemia initiating stem cells

    Journal: Cell reports

    doi: 10.1016/j.celrep.2023.112794


    Figure Legend Snippet:

    Techniques Used: Recombinant, Enzyme-linked Immunosorbent Assay, Binding Assay, Staining, Modification, Concentration Assay, Over Expression, Protein Extraction, SYBR Green Assay, Bicinchoninic Acid Protein Assay, Protease Inhibitor, CCK-8 Assay, Selection, Plasmid Preparation, Knock-Out, Software, Real-time Polymerase Chain Reaction, Flow Cytometry

    phospho akt ser473 193h12 rabbit mab  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phospho akt ser473 193h12 rabbit mab
    Phospho Akt Ser473 193h12 Rabbit Mab, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    rabbit monoclonal phospho akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit monoclonal phospho akt
    Rabbit Monoclonal Phospho Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    phospho akt thr308 c31e5e rabbit mab  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phospho akt thr308 c31e5e rabbit mab
    AHBA activated kinase signaling (A) cPLA2 phosphorylation and AHBA-induced LPA receptor activation. Total cPLA2 and its phosphorylated form were examined in TGPMs treated with the indicated inhibitors. (B) cPLA2 phosphorylation and AHBA-induced ERK activation. Total cPLA2 and its phosphorylated form were examined in TGPMs treated with the indicated inhibitors. (C) ERK phosphorylation and AHBA-induced LPA receptor activation. Total ERK and its phosphorylated form were examined in TGPMs treated with the indicated inhibitors. (D) AKT phosphorylation and AHBA-induced LPA receptor activation. Total AKT and its <t>Thr308-and</t> Ser473-phosphorylated forms were examined in TGPMs treated with the indicated inhibitors. The inhibitors used are the LPA receptor blocker H2L5765834, the TXA2 receptor blocker daltroban, the ERK inhibitor FR 180204, the ROCK inhibitor Y-27632, and the PI3K inhibitor TG100-116. Total cell lysates were prepared from TGPMs treated with the combination of inhibitors for 20 min and subjected to immune-blot analysis. The resulting immune-signals were captured as shown in the representative digital images and quantitatively analyzed as presented in the plot graphs. The relative abundance is related to the average level of the right-side group in each graph. The data represent means ± SEM., and the mice examined are shown in parentheses. Significant differences between the groups indicated by bars are statistically examined (ns: not significant, ∗p < 0.05 and ∗∗p < 0.01 in ANOVA and Sidak’s test).
    Phospho Akt Thr308 C31e5e Rabbit Mab, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/phospho akt thr308 c31e5e rabbit mab/product/Cell Signaling Technology Inc
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    Images

    1) Product Images from "Soluble epoxide hydrolase maintains steady-state lipid turnover linked with autocrine signaling in peritoneal macrophages"

    Article Title: Soluble epoxide hydrolase maintains steady-state lipid turnover linked with autocrine signaling in peritoneal macrophages

    Journal: iScience

    doi: 10.1016/j.isci.2023.107465

    AHBA activated kinase signaling (A) cPLA2 phosphorylation and AHBA-induced LPA receptor activation. Total cPLA2 and its phosphorylated form were examined in TGPMs treated with the indicated inhibitors. (B) cPLA2 phosphorylation and AHBA-induced ERK activation. Total cPLA2 and its phosphorylated form were examined in TGPMs treated with the indicated inhibitors. (C) ERK phosphorylation and AHBA-induced LPA receptor activation. Total ERK and its phosphorylated form were examined in TGPMs treated with the indicated inhibitors. (D) AKT phosphorylation and AHBA-induced LPA receptor activation. Total AKT and its Thr308-and Ser473-phosphorylated forms were examined in TGPMs treated with the indicated inhibitors. The inhibitors used are the LPA receptor blocker H2L5765834, the TXA2 receptor blocker daltroban, the ERK inhibitor FR 180204, the ROCK inhibitor Y-27632, and the PI3K inhibitor TG100-116. Total cell lysates were prepared from TGPMs treated with the combination of inhibitors for 20 min and subjected to immune-blot analysis. The resulting immune-signals were captured as shown in the representative digital images and quantitatively analyzed as presented in the plot graphs. The relative abundance is related to the average level of the right-side group in each graph. The data represent means ± SEM., and the mice examined are shown in parentheses. Significant differences between the groups indicated by bars are statistically examined (ns: not significant, ∗p < 0.05 and ∗∗p < 0.01 in ANOVA and Sidak’s test).
    Figure Legend Snippet: AHBA activated kinase signaling (A) cPLA2 phosphorylation and AHBA-induced LPA receptor activation. Total cPLA2 and its phosphorylated form were examined in TGPMs treated with the indicated inhibitors. (B) cPLA2 phosphorylation and AHBA-induced ERK activation. Total cPLA2 and its phosphorylated form were examined in TGPMs treated with the indicated inhibitors. (C) ERK phosphorylation and AHBA-induced LPA receptor activation. Total ERK and its phosphorylated form were examined in TGPMs treated with the indicated inhibitors. (D) AKT phosphorylation and AHBA-induced LPA receptor activation. Total AKT and its Thr308-and Ser473-phosphorylated forms were examined in TGPMs treated with the indicated inhibitors. The inhibitors used are the LPA receptor blocker H2L5765834, the TXA2 receptor blocker daltroban, the ERK inhibitor FR 180204, the ROCK inhibitor Y-27632, and the PI3K inhibitor TG100-116. Total cell lysates were prepared from TGPMs treated with the combination of inhibitors for 20 min and subjected to immune-blot analysis. The resulting immune-signals were captured as shown in the representative digital images and quantitatively analyzed as presented in the plot graphs. The relative abundance is related to the average level of the right-side group in each graph. The data represent means ± SEM., and the mice examined are shown in parentheses. Significant differences between the groups indicated by bars are statistically examined (ns: not significant, ∗p < 0.05 and ∗∗p < 0.01 in ANOVA and Sidak’s test).

    Techniques Used: Activation Assay


    Figure Legend Snippet:

    Techniques Used: Purification, Derivative Assay, Recombinant, Enzyme-linked Immunosorbent Assay, Chemotaxis Assay, H2O2 Assay, Microarray, Software

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    Cell Signaling Technology Inc phospho akt ser473 d9e xp rabbit mab
    Phospho Akt Ser473 D9e Xp Rabbit Mab, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Cell Signaling Technology Inc phospho akt rabbit mab
    The effect of aging <t>on</t> <t>IκBα</t> and <t>Akt</t> following hemorrhagic shock (trauma/hemorrhage, TH) and femoral fracture (Fx) in young (17-26 weeks) and aged (64-72 weeks) male C57BL/6J mice. The experimental design included young (17-26 weeks) and aged (64-72 weeks) C57BL/6J mice in both sham and trauma groups. The trauma groups underwent a pressure-controlled hemorrhagic shock and Fx (via osteotomy) (THFx), while the sham groups underwent catheterization and received an external fixator, but no THFx was induced. After twenty-four hours, the mice were euthanized, and sampling was performed. (A) Western blot analysis of phosphorylated and non-phosphorylated IκBα, AKT as well as β-Actin, and quantification of (B) the phosphorylation ratio of IκBα, and (C) AKT in liver tissue. n=4 in each group, *: p<0.05 between indicated groups.
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    AHBA activated kinase signaling (A) cPLA2 phosphorylation and AHBA-induced LPA receptor activation. Total cPLA2 and its phosphorylated form were examined in TGPMs treated with the indicated inhibitors. (B) cPLA2 phosphorylation and AHBA-induced ERK activation. Total cPLA2 and its phosphorylated form were examined in TGPMs treated with the indicated inhibitors. (C) ERK phosphorylation and AHBA-induced LPA receptor activation. Total ERK and its phosphorylated form were examined in TGPMs treated with the indicated inhibitors. (D) AKT phosphorylation and AHBA-induced LPA receptor activation. Total AKT and its <t>Thr308-and</t> Ser473-phosphorylated forms were examined in TGPMs treated with the indicated inhibitors. The inhibitors used are the LPA receptor blocker H2L5765834, the TXA2 receptor blocker daltroban, the ERK inhibitor FR 180204, the ROCK inhibitor Y-27632, and the PI3K inhibitor TG100-116. Total cell lysates were prepared from TGPMs treated with the combination of inhibitors for 20 min and subjected to immune-blot analysis. The resulting immune-signals were captured as shown in the representative digital images and quantitatively analyzed as presented in the plot graphs. The relative abundance is related to the average level of the right-side group in each graph. The data represent means ± SEM., and the mice examined are shown in parentheses. Significant differences between the groups indicated by bars are statistically examined (ns: not significant, ∗p < 0.05 and ∗∗p < 0.01 in ANOVA and Sidak’s test).
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    Image Search Results


    The effect of aging on IκBα and Akt following hemorrhagic shock (trauma/hemorrhage, TH) and femoral fracture (Fx) in young (17-26 weeks) and aged (64-72 weeks) male C57BL/6J mice. The experimental design included young (17-26 weeks) and aged (64-72 weeks) C57BL/6J mice in both sham and trauma groups. The trauma groups underwent a pressure-controlled hemorrhagic shock and Fx (via osteotomy) (THFx), while the sham groups underwent catheterization and received an external fixator, but no THFx was induced. After twenty-four hours, the mice were euthanized, and sampling was performed. (A) Western blot analysis of phosphorylated and non-phosphorylated IκBα, AKT as well as β-Actin, and quantification of (B) the phosphorylation ratio of IκBα, and (C) AKT in liver tissue. n=4 in each group, *: p<0.05 between indicated groups.

    Journal: Frontiers in Immunology

    Article Title: Impact of age on liver damage, inflammation, and molecular signaling pathways in response to femoral fracture and hemorrhage

    doi: 10.3389/fimmu.2023.1239145

    Figure Lengend Snippet: The effect of aging on IκBα and Akt following hemorrhagic shock (trauma/hemorrhage, TH) and femoral fracture (Fx) in young (17-26 weeks) and aged (64-72 weeks) male C57BL/6J mice. The experimental design included young (17-26 weeks) and aged (64-72 weeks) C57BL/6J mice in both sham and trauma groups. The trauma groups underwent a pressure-controlled hemorrhagic shock and Fx (via osteotomy) (THFx), while the sham groups underwent catheterization and received an external fixator, but no THFx was induced. After twenty-four hours, the mice were euthanized, and sampling was performed. (A) Western blot analysis of phosphorylated and non-phosphorylated IκBα, AKT as well as β-Actin, and quantification of (B) the phosphorylation ratio of IκBα, and (C) AKT in liver tissue. n=4 in each group, *: p<0.05 between indicated groups.

    Article Snippet: IκBα Rabbit polyclonal antibody (9242S, 1:1000), Phospho-IκBα Mouse mAb (9246S, 1:1000), Akt Rabbit mAb (4691S, 1:1000), and Phospho-Akt Rabbit mAb (4060S, 1: 2000, all Cell Signaling Technology) were used as primary antibodies.

    Techniques: Sampling, Western Blot

    Journal: iScience

    Article Title: mTORC2 regulates auditory hair cell structure and function

    doi: 10.1016/j.isci.2023.107687

    Figure Lengend Snippet:

    Article Snippet: Rabbit monoclonal anti-phospho-Akt (Ser473) IgG , Cell Signaling Technology , Cat#4060; RRID: AB_2315049.

    Techniques: Recombinant, Saline, Electron Microscopy, Software, Imaging

    Journal: iScience

    Article Title: Activation of AKT induces EZH2-mediated β-catenin trimethylation in colorectal cancer

    doi: 10.1016/j.isci.2023.107630

    Figure Lengend Snippet:

    Article Snippet: Rabbit monoclonal anti- Phospho-Akt Substrate (RXXS∗/T∗) , Cell Signaling Technology , Cat#9614, RRID: AB_331810.

    Techniques: Virus, shRNA, Plasmid Preparation, Recombinant, Protease Inhibitor, DNA Purification, Mutagenesis, Software

    Journal: Cell reports

    Article Title: Activation of GPR44 decreases severity of myeloid leukemia via specific targeting of leukemia initiating stem cells

    doi: 10.1016/j.celrep.2023.112794

    Figure Lengend Snippet:

    Article Snippet: Rabbit monoclonal anti-Phospho-Akt (Ser473) (D9E) XP ® , Cell Signaling Technology , Cat# 4060; RRID: AB_2315049.

    Techniques: Recombinant, Enzyme-linked Immunosorbent Assay, Binding Assay, Staining, Modification, Concentration Assay, Over Expression, Protein Extraction, SYBR Green Assay, Bicinchoninic Acid Protein Assay, Protease Inhibitor, CCK-8 Assay, Selection, Plasmid Preparation, Knock-Out, Software, Real-time Polymerase Chain Reaction, Flow Cytometry

    AHBA activated kinase signaling (A) cPLA2 phosphorylation and AHBA-induced LPA receptor activation. Total cPLA2 and its phosphorylated form were examined in TGPMs treated with the indicated inhibitors. (B) cPLA2 phosphorylation and AHBA-induced ERK activation. Total cPLA2 and its phosphorylated form were examined in TGPMs treated with the indicated inhibitors. (C) ERK phosphorylation and AHBA-induced LPA receptor activation. Total ERK and its phosphorylated form were examined in TGPMs treated with the indicated inhibitors. (D) AKT phosphorylation and AHBA-induced LPA receptor activation. Total AKT and its Thr308-and Ser473-phosphorylated forms were examined in TGPMs treated with the indicated inhibitors. The inhibitors used are the LPA receptor blocker H2L5765834, the TXA2 receptor blocker daltroban, the ERK inhibitor FR 180204, the ROCK inhibitor Y-27632, and the PI3K inhibitor TG100-116. Total cell lysates were prepared from TGPMs treated with the combination of inhibitors for 20 min and subjected to immune-blot analysis. The resulting immune-signals were captured as shown in the representative digital images and quantitatively analyzed as presented in the plot graphs. The relative abundance is related to the average level of the right-side group in each graph. The data represent means ± SEM., and the mice examined are shown in parentheses. Significant differences between the groups indicated by bars are statistically examined (ns: not significant, ∗p < 0.05 and ∗∗p < 0.01 in ANOVA and Sidak’s test).

    Journal: iScience

    Article Title: Soluble epoxide hydrolase maintains steady-state lipid turnover linked with autocrine signaling in peritoneal macrophages

    doi: 10.1016/j.isci.2023.107465

    Figure Lengend Snippet: AHBA activated kinase signaling (A) cPLA2 phosphorylation and AHBA-induced LPA receptor activation. Total cPLA2 and its phosphorylated form were examined in TGPMs treated with the indicated inhibitors. (B) cPLA2 phosphorylation and AHBA-induced ERK activation. Total cPLA2 and its phosphorylated form were examined in TGPMs treated with the indicated inhibitors. (C) ERK phosphorylation and AHBA-induced LPA receptor activation. Total ERK and its phosphorylated form were examined in TGPMs treated with the indicated inhibitors. (D) AKT phosphorylation and AHBA-induced LPA receptor activation. Total AKT and its Thr308-and Ser473-phosphorylated forms were examined in TGPMs treated with the indicated inhibitors. The inhibitors used are the LPA receptor blocker H2L5765834, the TXA2 receptor blocker daltroban, the ERK inhibitor FR 180204, the ROCK inhibitor Y-27632, and the PI3K inhibitor TG100-116. Total cell lysates were prepared from TGPMs treated with the combination of inhibitors for 20 min and subjected to immune-blot analysis. The resulting immune-signals were captured as shown in the representative digital images and quantitatively analyzed as presented in the plot graphs. The relative abundance is related to the average level of the right-side group in each graph. The data represent means ± SEM., and the mice examined are shown in parentheses. Significant differences between the groups indicated by bars are statistically examined (ns: not significant, ∗p < 0.05 and ∗∗p < 0.01 in ANOVA and Sidak’s test).

    Article Snippet: Phospho-Akt (Thr308) (C31E5E) Rabbit mAb , Cell Signaling Technology , Cat#2965; RRID: AB_2255933.

    Techniques: Activation Assay

    Journal: iScience

    Article Title: Soluble epoxide hydrolase maintains steady-state lipid turnover linked with autocrine signaling in peritoneal macrophages

    doi: 10.1016/j.isci.2023.107465

    Figure Lengend Snippet:

    Article Snippet: Phospho-Akt (Thr308) (C31E5E) Rabbit mAb , Cell Signaling Technology , Cat#2965; RRID: AB_2255933.

    Techniques: Purification, Derivative Assay, Recombinant, Enzyme-linked Immunosorbent Assay, Chemotaxis Assay, H2O2 Assay, Microarray, Software