phospho akt308  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phospho akt308
    Phospho Akt308, 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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    phospho akt308  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phospho akt308
    K562 cells with or without ME2 knockdown were lysed with RIPA lysis buffer (50 mM Tris-HCl, pH 8.0, 150 mM NaCl, 1% Triton X-100, 1 mM EGTA) containing 1 mM PMSF and a protease inhibitor cocktail and subjected to centrifugation at 15,000× g for 10 min at 4°C to remove debris. After lysis, equal aliquots of protein lysate were resolved by Western blotting. Western blots were probed with anti-phospho-ERK1/2, anti-ERK1, <t>anti-p-AKT308,</t> anti-AKT472, anti-AKT1/2, anti-GATA-1, anti-vimentin and anti-β-tubulin. A, phospho-ERK1/2 activity in ME2 knockdown K562 cells. B, Phospho-AKT detection in ME2 knockdown K562 cells. C, 10 µM PI3K inhibitor, LY294002, inhibits p-AKT activity. D, LY294002 rescue of differentiation in ME2 knockdown K562 cells. E, The effect of LY294002 on the proliferation of K562 cells with or without ME2 knockdown. F, The expression difference of GATA-1 and vimentin in ME2 knockdown cells. Data are representative of three independent experiments.
    Phospho Akt308, 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 "Induction of Erythroid Differentiation in Human Erythroleukemia Cells by Depletion of Malic Enzyme 2"

    Article Title: Induction of Erythroid Differentiation in Human Erythroleukemia Cells by Depletion of Malic Enzyme 2

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0012520

    K562 cells with or without ME2 knockdown were lysed with RIPA lysis buffer (50 mM Tris-HCl, pH 8.0, 150 mM NaCl, 1% Triton X-100, 1 mM EGTA) containing 1 mM PMSF and a protease inhibitor cocktail and subjected to centrifugation at 15,000× g for 10 min at 4°C to remove debris. After lysis, equal aliquots of protein lysate were resolved by Western blotting. Western blots were probed with anti-phospho-ERK1/2, anti-ERK1, anti-p-AKT308, anti-AKT472, anti-AKT1/2, anti-GATA-1, anti-vimentin and anti-β-tubulin. A, phospho-ERK1/2 activity in ME2 knockdown K562 cells. B, Phospho-AKT detection in ME2 knockdown K562 cells. C, 10 µM PI3K inhibitor, LY294002, inhibits p-AKT activity. D, LY294002 rescue of differentiation in ME2 knockdown K562 cells. E, The effect of LY294002 on the proliferation of K562 cells with or without ME2 knockdown. F, The expression difference of GATA-1 and vimentin in ME2 knockdown cells. Data are representative of three independent experiments.
    Figure Legend Snippet: K562 cells with or without ME2 knockdown were lysed with RIPA lysis buffer (50 mM Tris-HCl, pH 8.0, 150 mM NaCl, 1% Triton X-100, 1 mM EGTA) containing 1 mM PMSF and a protease inhibitor cocktail and subjected to centrifugation at 15,000× g for 10 min at 4°C to remove debris. After lysis, equal aliquots of protein lysate were resolved by Western blotting. Western blots were probed with anti-phospho-ERK1/2, anti-ERK1, anti-p-AKT308, anti-AKT472, anti-AKT1/2, anti-GATA-1, anti-vimentin and anti-β-tubulin. A, phospho-ERK1/2 activity in ME2 knockdown K562 cells. B, Phospho-AKT detection in ME2 knockdown K562 cells. C, 10 µM PI3K inhibitor, LY294002, inhibits p-AKT activity. D, LY294002 rescue of differentiation in ME2 knockdown K562 cells. E, The effect of LY294002 on the proliferation of K562 cells with or without ME2 knockdown. F, The expression difference of GATA-1 and vimentin in ME2 knockdown cells. Data are representative of three independent experiments.

    Techniques Used: Lysis, Protease Inhibitor, Centrifugation, Western Blot, Activity Assay, Expressing

    phospho akt308  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phospho akt308
    Phospho Akt308, 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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    phospho akt308  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phospho akt308
    Phospho Akt308, 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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    anti p akt308  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc anti p akt308
    Primary brown adipocytes were isolated, cultured, and treated with Ang-(1-7) (10 –6 M) for 24 hr, Akt inhibitor MK2206 (20 μM) for 24 hr, PKA inhibitor H89 (30 μM) for 24 hr, or adenylylcyclase inhibitor SQ-22536 (10 μM) for 24 hours. ( A, B ) Representative western blots showing the changes of <t>p-Akt308</t> and Akt in BAT of Ace2 -/y ( A ) and Lepr db/db + Ace2 mice ( B ) exposure at 4 °C (n = 3/each group). ( C ) Representative western blots showing the Akt, UCP1 and forkhead box protein O 1 (FoxO1) Changes (n = 3/each group). ( D ) Relative mRNA levels of thermogenic and mitochondrial genes (n = 4–6/each group). ( E ) Continuous measurement of oxygen consumption rate (OCR) in Ang-(1-7) and MK2206 treated primary brown adipocytes. Oxygen consumption was performed under basal conditions, following the addition of oligomycin (1 μM), the pharmacological uncoupler FCCP (1 μM) or the Complex III and I inhibitor antimycin A and rotenone (0.5 μM) (n = 3–4/each group). ( F, G ) Representative western blots showing the p-PKA and PKA changes in BAT of Ace2 -/y ( F ) and Lepr db/db + Ace2 mice ( G ) exposure at 4 °C (n = 3/each group). ( H ) Relative mRNA levels of thermogenic and mitochondrial genes (n = 4–6/each group). ( I ) Representative western blots showing the UCP1 and PGC1α changes (n = 3/each group). ( J ) Continuous measurement of OCR in Ang-(1-7) and H89-treated primary brown Adipocytes (n = 3–5/each group). Data represent mean ± SEM. *p< 0.05, **p < 0.01 vs GFP/WT group by Student’s t -test. *p < 0.05, **p < 0.01 vs control group, # p < 0.05, ## p < 0.01 vs Ang-(1-7) group by one-way ANOVA. ( K ) Mechanisms involved in ACE2 pathway activation-induced improvement of BAT function.
    Anti P Akt308, 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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    1) Product Images from "ACE2 pathway regulates thermogenesis and energy metabolism"

    Article Title: ACE2 pathway regulates thermogenesis and energy metabolism

    Journal: eLife

    doi: 10.7554/eLife.72266

    Primary brown adipocytes were isolated, cultured, and treated with Ang-(1-7) (10 –6 M) for 24 hr, Akt inhibitor MK2206 (20 μM) for 24 hr, PKA inhibitor H89 (30 μM) for 24 hr, or adenylylcyclase inhibitor SQ-22536 (10 μM) for 24 hours. ( A, B ) Representative western blots showing the changes of p-Akt308 and Akt in BAT of Ace2 -/y ( A ) and Lepr db/db + Ace2 mice ( B ) exposure at 4 °C (n = 3/each group). ( C ) Representative western blots showing the Akt, UCP1 and forkhead box protein O 1 (FoxO1) Changes (n = 3/each group). ( D ) Relative mRNA levels of thermogenic and mitochondrial genes (n = 4–6/each group). ( E ) Continuous measurement of oxygen consumption rate (OCR) in Ang-(1-7) and MK2206 treated primary brown adipocytes. Oxygen consumption was performed under basal conditions, following the addition of oligomycin (1 μM), the pharmacological uncoupler FCCP (1 μM) or the Complex III and I inhibitor antimycin A and rotenone (0.5 μM) (n = 3–4/each group). ( F, G ) Representative western blots showing the p-PKA and PKA changes in BAT of Ace2 -/y ( F ) and Lepr db/db + Ace2 mice ( G ) exposure at 4 °C (n = 3/each group). ( H ) Relative mRNA levels of thermogenic and mitochondrial genes (n = 4–6/each group). ( I ) Representative western blots showing the UCP1 and PGC1α changes (n = 3/each group). ( J ) Continuous measurement of OCR in Ang-(1-7) and H89-treated primary brown Adipocytes (n = 3–5/each group). Data represent mean ± SEM. *p< 0.05, **p < 0.01 vs GFP/WT group by Student’s t -test. *p < 0.05, **p < 0.01 vs control group, # p < 0.05, ## p < 0.01 vs Ang-(1-7) group by one-way ANOVA. ( K ) Mechanisms involved in ACE2 pathway activation-induced improvement of BAT function.
    Figure Legend Snippet: Primary brown adipocytes were isolated, cultured, and treated with Ang-(1-7) (10 –6 M) for 24 hr, Akt inhibitor MK2206 (20 μM) for 24 hr, PKA inhibitor H89 (30 μM) for 24 hr, or adenylylcyclase inhibitor SQ-22536 (10 μM) for 24 hours. ( A, B ) Representative western blots showing the changes of p-Akt308 and Akt in BAT of Ace2 -/y ( A ) and Lepr db/db + Ace2 mice ( B ) exposure at 4 °C (n = 3/each group). ( C ) Representative western blots showing the Akt, UCP1 and forkhead box protein O 1 (FoxO1) Changes (n = 3/each group). ( D ) Relative mRNA levels of thermogenic and mitochondrial genes (n = 4–6/each group). ( E ) Continuous measurement of oxygen consumption rate (OCR) in Ang-(1-7) and MK2206 treated primary brown adipocytes. Oxygen consumption was performed under basal conditions, following the addition of oligomycin (1 μM), the pharmacological uncoupler FCCP (1 μM) or the Complex III and I inhibitor antimycin A and rotenone (0.5 μM) (n = 3–4/each group). ( F, G ) Representative western blots showing the p-PKA and PKA changes in BAT of Ace2 -/y ( F ) and Lepr db/db + Ace2 mice ( G ) exposure at 4 °C (n = 3/each group). ( H ) Relative mRNA levels of thermogenic and mitochondrial genes (n = 4–6/each group). ( I ) Representative western blots showing the UCP1 and PGC1α changes (n = 3/each group). ( J ) Continuous measurement of OCR in Ang-(1-7) and H89-treated primary brown Adipocytes (n = 3–5/each group). Data represent mean ± SEM. *p< 0.05, **p < 0.01 vs GFP/WT group by Student’s t -test. *p < 0.05, **p < 0.01 vs control group, # p < 0.05, ## p < 0.01 vs Ang-(1-7) group by one-way ANOVA. ( K ) Mechanisms involved in ACE2 pathway activation-induced improvement of BAT function.

    Techniques Used: Isolation, Cell Culture, Western Blot, Activation Assay


    Figure Legend Snippet:

    Techniques Used: Transfection, Construct, Sequencing, Software

    anti p akt308  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc anti p akt308
    Primary brown adipocytes were isolated, cultured, and treated with Ang-(1-7) (10 –6 M) for 24 hr, Akt inhibitor MK2206 (20 μM) for 24 hr, PKA inhibitor H89 (30 μM) for 24 hr, or adenylylcyclase inhibitor SQ-22536 (10 μM) for 24 hours. ( A, B ) Representative western blots showing the changes of <t>p-Akt308</t> and Akt in BAT of Ace2 -/y ( A ) and Lepr db/db + Ace2 mice ( B ) exposure at 4 °C (n = 3/each group). ( C ) Representative western blots showing the Akt, UCP1 and forkhead box protein O 1 (FoxO1) Changes (n = 3/each group). ( D ) Relative mRNA levels of thermogenic and mitochondrial genes (n = 4–6/each group). ( E ) Continuous measurement of oxygen consumption rate (OCR) in Ang-(1-7) and MK2206 treated primary brown adipocytes. Oxygen consumption was performed under basal conditions, following the addition of oligomycin (1 μM), the pharmacological uncoupler FCCP (1 μM) or the Complex III and I inhibitor antimycin A and rotenone (0.5 μM) (n = 3–4/each group). ( F, G ) Representative western blots showing the p-PKA and PKA changes in BAT of Ace2 -/y ( F ) and Lepr db/db + Ace2 mice ( G ) exposure at 4 °C (n = 3/each group). ( H ) Relative mRNA levels of thermogenic and mitochondrial genes (n = 4–6/each group). ( I ) Representative western blots showing the UCP1 and PGC1α changes (n = 3/each group). ( J ) Continuous measurement of OCR in Ang-(1-7) and H89-treated primary brown Adipocytes (n = 3–5/each group). Data represent mean ± SEM. *p< 0.05, **p < 0.01 vs GFP/WT group by Student’s t -test. *p < 0.05, **p < 0.01 vs control group, # p < 0.05, ## p < 0.01 vs Ang-(1-7) group by one-way ANOVA. ( K ) Mechanisms involved in ACE2 pathway activation-induced improvement of BAT function.
    Anti P Akt308, 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/result/anti p akt308/product/Cell Signaling Technology Inc
    Average 96 stars, based on 1 article reviews
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    anti p akt308 - by Bioz Stars, 2023-04
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    1) Product Images from "ACE2 pathway regulates thermogenesis and energy metabolism"

    Article Title: ACE2 pathway regulates thermogenesis and energy metabolism

    Journal: eLife

    doi: 10.7554/eLife.72266

    Primary brown adipocytes were isolated, cultured, and treated with Ang-(1-7) (10 –6 M) for 24 hr, Akt inhibitor MK2206 (20 μM) for 24 hr, PKA inhibitor H89 (30 μM) for 24 hr, or adenylylcyclase inhibitor SQ-22536 (10 μM) for 24 hours. ( A, B ) Representative western blots showing the changes of p-Akt308 and Akt in BAT of Ace2 -/y ( A ) and Lepr db/db + Ace2 mice ( B ) exposure at 4 °C (n = 3/each group). ( C ) Representative western blots showing the Akt, UCP1 and forkhead box protein O 1 (FoxO1) Changes (n = 3/each group). ( D ) Relative mRNA levels of thermogenic and mitochondrial genes (n = 4–6/each group). ( E ) Continuous measurement of oxygen consumption rate (OCR) in Ang-(1-7) and MK2206 treated primary brown adipocytes. Oxygen consumption was performed under basal conditions, following the addition of oligomycin (1 μM), the pharmacological uncoupler FCCP (1 μM) or the Complex III and I inhibitor antimycin A and rotenone (0.5 μM) (n = 3–4/each group). ( F, G ) Representative western blots showing the p-PKA and PKA changes in BAT of Ace2 -/y ( F ) and Lepr db/db + Ace2 mice ( G ) exposure at 4 °C (n = 3/each group). ( H ) Relative mRNA levels of thermogenic and mitochondrial genes (n = 4–6/each group). ( I ) Representative western blots showing the UCP1 and PGC1α changes (n = 3/each group). ( J ) Continuous measurement of OCR in Ang-(1-7) and H89-treated primary brown Adipocytes (n = 3–5/each group). Data represent mean ± SEM. *p< 0.05, **p < 0.01 vs GFP/WT group by Student’s t -test. *p < 0.05, **p < 0.01 vs control group, # p < 0.05, ## p < 0.01 vs Ang-(1-7) group by one-way ANOVA. ( K ) Mechanisms involved in ACE2 pathway activation-induced improvement of BAT function.
    Figure Legend Snippet: Primary brown adipocytes were isolated, cultured, and treated with Ang-(1-7) (10 –6 M) for 24 hr, Akt inhibitor MK2206 (20 μM) for 24 hr, PKA inhibitor H89 (30 μM) for 24 hr, or adenylylcyclase inhibitor SQ-22536 (10 μM) for 24 hours. ( A, B ) Representative western blots showing the changes of p-Akt308 and Akt in BAT of Ace2 -/y ( A ) and Lepr db/db + Ace2 mice ( B ) exposure at 4 °C (n = 3/each group). ( C ) Representative western blots showing the Akt, UCP1 and forkhead box protein O 1 (FoxO1) Changes (n = 3/each group). ( D ) Relative mRNA levels of thermogenic and mitochondrial genes (n = 4–6/each group). ( E ) Continuous measurement of oxygen consumption rate (OCR) in Ang-(1-7) and MK2206 treated primary brown adipocytes. Oxygen consumption was performed under basal conditions, following the addition of oligomycin (1 μM), the pharmacological uncoupler FCCP (1 μM) or the Complex III and I inhibitor antimycin A and rotenone (0.5 μM) (n = 3–4/each group). ( F, G ) Representative western blots showing the p-PKA and PKA changes in BAT of Ace2 -/y ( F ) and Lepr db/db + Ace2 mice ( G ) exposure at 4 °C (n = 3/each group). ( H ) Relative mRNA levels of thermogenic and mitochondrial genes (n = 4–6/each group). ( I ) Representative western blots showing the UCP1 and PGC1α changes (n = 3/each group). ( J ) Continuous measurement of OCR in Ang-(1-7) and H89-treated primary brown Adipocytes (n = 3–5/each group). Data represent mean ± SEM. *p< 0.05, **p < 0.01 vs GFP/WT group by Student’s t -test. *p < 0.05, **p < 0.01 vs control group, # p < 0.05, ## p < 0.01 vs Ang-(1-7) group by one-way ANOVA. ( K ) Mechanisms involved in ACE2 pathway activation-induced improvement of BAT function.

    Techniques Used: Isolation, Cell Culture, Western Blot, Activation Assay


    Figure Legend Snippet:

    Techniques Used: Transfection, Construct, Sequencing, Software

    phospho akt308  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phospho akt308
    Phospho Akt308, 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/result/phospho akt308/product/Cell Signaling Technology Inc
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    anti p akt308  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc anti p akt308
    Primary brown adipocytes were isolated, cultured, and treated with Ang-(1-7) (10 −6 M) for 24 hours, Akt inhibitor MK2206 (30μM) for 24 hours, PKA inhibitor H89 (30μM) for 2 hours, or adenylylcyclase inhibitor SQ-22536 (10μM) for 24 hours. (A, B) Representative western blots showing the changes of <t>p-Akt308</t> and Akt in BAT of ACE2 -/y ( A ) and db/db+ACE2 mice ( B ) exposure at 4°C. n =3/each group. (C) Representative western blots showing the Akt, uncoupling protein-1 (UCP1) and forkhead box protein O1 (FOXO1) changes. n=3/each group. (D) Relative mRNA levels of thermogenic and mitochondrial genes. n=4-6/each group. (E) Continuous measurement of oxygen consumption rate (OCR). Oxygen consumption was performed under basal conditions, following the addition of oligomycin (14μM), the pharmacological uncoupler FCCP (10μM) or the Complex III and I inhibitor antimycin A and rotenone (4μM each). n =5-7/each group. (F, G) Representative western blots showing the p-PKA and PKA changes in BAT of ACE2 -/y ( F ) and db/db+ACE2 mice ( G ) exposure at 4°C. n =3/each group. (H) Relative mRNA levels of thermogenic and mitochondrial genes. n=4-6/each group. (I) Representative western blots showing the UCP1 and PGC-1α changes. n=4/each group. (J) Continuous measurement of OCR. Oxygen consumption was performed under basal conditions, following the addition of oligomycin, the pharmacological uncoupler FCCP (10μM) or the Complex III and I inhibitor antimycin A and rotenone (4μM each). N =5-7/each group. Data represent mean ± SEM; * p < 0.05, ** p < 0.01 vs control group by Student’s test. # p < 0.05, ## p < 0.01 vs Ang-(1-7) group by Student’s t -test. (K) Mechanisms involved in ACE2 pathway activation-induced improvement of BAT function. The online version of this article includes the following figure supplement(s) for : . RNA-Seq analysis of primary brown adipocytes from ACE2 -/y and WT mice; Ang-(1-7) regulates thermogenesis through Akt and PKA signaling in BAT. . Ang-(1-7) regulates thermogenesis through Akt and PKA signaling in BAT.
    Anti P Akt308, 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/result/anti p akt308/product/Cell Signaling Technology Inc
    Average 96 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    anti p akt308 - by Bioz Stars, 2023-04
    96/100 stars

    Images

    1) Product Images from "ACE2 Pathway Regulates Thermogenesis and Energy Metabolism"

    Article Title: ACE2 Pathway Regulates Thermogenesis and Energy Metabolism

    Journal: bioRxiv

    doi: 10.1101/2021.08.10.455823

    Primary brown adipocytes were isolated, cultured, and treated with Ang-(1-7) (10 −6 M) for 24 hours, Akt inhibitor MK2206 (30μM) for 24 hours, PKA inhibitor H89 (30μM) for 2 hours, or adenylylcyclase inhibitor SQ-22536 (10μM) for 24 hours. (A, B) Representative western blots showing the changes of p-Akt308 and Akt in BAT of ACE2 -/y ( A ) and db/db+ACE2 mice ( B ) exposure at 4°C. n =3/each group. (C) Representative western blots showing the Akt, uncoupling protein-1 (UCP1) and forkhead box protein O1 (FOXO1) changes. n=3/each group. (D) Relative mRNA levels of thermogenic and mitochondrial genes. n=4-6/each group. (E) Continuous measurement of oxygen consumption rate (OCR). Oxygen consumption was performed under basal conditions, following the addition of oligomycin (14μM), the pharmacological uncoupler FCCP (10μM) or the Complex III and I inhibitor antimycin A and rotenone (4μM each). n =5-7/each group. (F, G) Representative western blots showing the p-PKA and PKA changes in BAT of ACE2 -/y ( F ) and db/db+ACE2 mice ( G ) exposure at 4°C. n =3/each group. (H) Relative mRNA levels of thermogenic and mitochondrial genes. n=4-6/each group. (I) Representative western blots showing the UCP1 and PGC-1α changes. n=4/each group. (J) Continuous measurement of OCR. Oxygen consumption was performed under basal conditions, following the addition of oligomycin, the pharmacological uncoupler FCCP (10μM) or the Complex III and I inhibitor antimycin A and rotenone (4μM each). N =5-7/each group. Data represent mean ± SEM; * p < 0.05, ** p < 0.01 vs control group by Student’s test. # p < 0.05, ## p < 0.01 vs Ang-(1-7) group by Student’s t -test. (K) Mechanisms involved in ACE2 pathway activation-induced improvement of BAT function. The online version of this article includes the following figure supplement(s) for : . RNA-Seq analysis of primary brown adipocytes from ACE2 -/y and WT mice; Ang-(1-7) regulates thermogenesis through Akt and PKA signaling in BAT. . Ang-(1-7) regulates thermogenesis through Akt and PKA signaling in BAT.
    Figure Legend Snippet: Primary brown adipocytes were isolated, cultured, and treated with Ang-(1-7) (10 −6 M) for 24 hours, Akt inhibitor MK2206 (30μM) for 24 hours, PKA inhibitor H89 (30μM) for 2 hours, or adenylylcyclase inhibitor SQ-22536 (10μM) for 24 hours. (A, B) Representative western blots showing the changes of p-Akt308 and Akt in BAT of ACE2 -/y ( A ) and db/db+ACE2 mice ( B ) exposure at 4°C. n =3/each group. (C) Representative western blots showing the Akt, uncoupling protein-1 (UCP1) and forkhead box protein O1 (FOXO1) changes. n=3/each group. (D) Relative mRNA levels of thermogenic and mitochondrial genes. n=4-6/each group. (E) Continuous measurement of oxygen consumption rate (OCR). Oxygen consumption was performed under basal conditions, following the addition of oligomycin (14μM), the pharmacological uncoupler FCCP (10μM) or the Complex III and I inhibitor antimycin A and rotenone (4μM each). n =5-7/each group. (F, G) Representative western blots showing the p-PKA and PKA changes in BAT of ACE2 -/y ( F ) and db/db+ACE2 mice ( G ) exposure at 4°C. n =3/each group. (H) Relative mRNA levels of thermogenic and mitochondrial genes. n=4-6/each group. (I) Representative western blots showing the UCP1 and PGC-1α changes. n=4/each group. (J) Continuous measurement of OCR. Oxygen consumption was performed under basal conditions, following the addition of oligomycin, the pharmacological uncoupler FCCP (10μM) or the Complex III and I inhibitor antimycin A and rotenone (4μM each). N =5-7/each group. Data represent mean ± SEM; * p < 0.05, ** p < 0.01 vs control group by Student’s test. # p < 0.05, ## p < 0.01 vs Ang-(1-7) group by Student’s t -test. (K) Mechanisms involved in ACE2 pathway activation-induced improvement of BAT function. The online version of this article includes the following figure supplement(s) for : . RNA-Seq analysis of primary brown adipocytes from ACE2 -/y and WT mice; Ang-(1-7) regulates thermogenesis through Akt and PKA signaling in BAT. . Ang-(1-7) regulates thermogenesis through Akt and PKA signaling in BAT.

    Techniques Used: Isolation, Cell Culture, Western Blot, Activation Assay, RNA Sequencing Assay

    western blot primary antibodies against p akt308  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc western blot primary antibodies against p akt308
    Western Blot Primary Antibodies Against P Akt308, 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/result/western blot primary antibodies against p akt308/product/Cell Signaling Technology Inc
    Average 96 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    western blot primary antibodies against p akt308 - by Bioz Stars, 2023-04
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    p akt308  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc p akt308
    Knockdown of ET-1 blocked the PI3K/Akt pathway. Western blot was performed to detect the level of p-PI3K, PI3K, p-Akt473, <t>p-Akt308</t> and Akt in ECA109 cells. ***, P<0.001, compared with the control group; ### , P<0.001, compared with the si-ET-1 group.
    P Akt308, 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/result/p akt308/product/Cell Signaling Technology Inc
    Average 96 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    p akt308 - by Bioz Stars, 2023-04
    96/100 stars

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    1) Product Images from "ET-1 promotes the growth and metastasis of esophageal squamous cell carcinoma via activating PI3K/Akt pathway"

    Article Title: ET-1 promotes the growth and metastasis of esophageal squamous cell carcinoma via activating PI3K/Akt pathway

    Journal: Translational Cancer Research

    doi: 10.21037/tcr.2020.04.26

    Knockdown of ET-1 blocked the PI3K/Akt pathway. Western blot was performed to detect the level of p-PI3K, PI3K, p-Akt473, p-Akt308 and Akt in ECA109 cells. ***, P<0.001, compared with the control group; ### , P<0.001, compared with the si-ET-1 group.
    Figure Legend Snippet: Knockdown of ET-1 blocked the PI3K/Akt pathway. Western blot was performed to detect the level of p-PI3K, PI3K, p-Akt473, p-Akt308 and Akt in ECA109 cells. ***, P<0.001, compared with the control group; ### , P<0.001, compared with the si-ET-1 group.

    Techniques Used: Western Blot

    phos akt308  (Cell Signaling Technology Inc)


    Bioz Verified Symbol Cell Signaling Technology Inc is a verified supplier
    Bioz Manufacturer Symbol Cell Signaling Technology Inc manufactures this product  
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    Cell Signaling Technology Inc phos akt308
    Phos Akt308, 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/result/phos akt308/product/Cell Signaling Technology Inc
    Average 96 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    phos akt308 - by Bioz Stars, 2023-04
    96/100 stars

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    Cell Signaling Technology Inc phospho akt308
    Phospho Akt308, 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 anti p akt308
    Primary brown adipocytes were isolated, cultured, and treated with Ang-(1-7) (10 –6 M) for 24 hr, Akt inhibitor MK2206 (20 μM) for 24 hr, PKA inhibitor H89 (30 μM) for 24 hr, or adenylylcyclase inhibitor SQ-22536 (10 μM) for 24 hours. ( A, B ) Representative western blots showing the changes of <t>p-Akt308</t> and Akt in BAT of Ace2 -/y ( A ) and Lepr db/db + Ace2 mice ( B ) exposure at 4 °C (n = 3/each group). ( C ) Representative western blots showing the Akt, UCP1 and forkhead box protein O 1 (FoxO1) Changes (n = 3/each group). ( D ) Relative mRNA levels of thermogenic and mitochondrial genes (n = 4–6/each group). ( E ) Continuous measurement of oxygen consumption rate (OCR) in Ang-(1-7) and MK2206 treated primary brown adipocytes. Oxygen consumption was performed under basal conditions, following the addition of oligomycin (1 μM), the pharmacological uncoupler FCCP (1 μM) or the Complex III and I inhibitor antimycin A and rotenone (0.5 μM) (n = 3–4/each group). ( F, G ) Representative western blots showing the p-PKA and PKA changes in BAT of Ace2 -/y ( F ) and Lepr db/db + Ace2 mice ( G ) exposure at 4 °C (n = 3/each group). ( H ) Relative mRNA levels of thermogenic and mitochondrial genes (n = 4–6/each group). ( I ) Representative western blots showing the UCP1 and PGC1α changes (n = 3/each group). ( J ) Continuous measurement of OCR in Ang-(1-7) and H89-treated primary brown Adipocytes (n = 3–5/each group). Data represent mean ± SEM. *p< 0.05, **p < 0.01 vs GFP/WT group by Student’s t -test. *p < 0.05, **p < 0.01 vs control group, # p < 0.05, ## p < 0.01 vs Ang-(1-7) group by one-way ANOVA. ( K ) Mechanisms involved in ACE2 pathway activation-induced improvement of BAT function.
    Anti P Akt308, 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/result/anti p akt308/product/Cell Signaling Technology Inc
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    Cell Signaling Technology Inc western blot primary antibodies against p akt308
    Primary brown adipocytes were isolated, cultured, and treated with Ang-(1-7) (10 –6 M) for 24 hr, Akt inhibitor MK2206 (20 μM) for 24 hr, PKA inhibitor H89 (30 μM) for 24 hr, or adenylylcyclase inhibitor SQ-22536 (10 μM) for 24 hours. ( A, B ) Representative western blots showing the changes of <t>p-Akt308</t> and Akt in BAT of Ace2 -/y ( A ) and Lepr db/db + Ace2 mice ( B ) exposure at 4 °C (n = 3/each group). ( C ) Representative western blots showing the Akt, UCP1 and forkhead box protein O 1 (FoxO1) Changes (n = 3/each group). ( D ) Relative mRNA levels of thermogenic and mitochondrial genes (n = 4–6/each group). ( E ) Continuous measurement of oxygen consumption rate (OCR) in Ang-(1-7) and MK2206 treated primary brown adipocytes. Oxygen consumption was performed under basal conditions, following the addition of oligomycin (1 μM), the pharmacological uncoupler FCCP (1 μM) or the Complex III and I inhibitor antimycin A and rotenone (0.5 μM) (n = 3–4/each group). ( F, G ) Representative western blots showing the p-PKA and PKA changes in BAT of Ace2 -/y ( F ) and Lepr db/db + Ace2 mice ( G ) exposure at 4 °C (n = 3/each group). ( H ) Relative mRNA levels of thermogenic and mitochondrial genes (n = 4–6/each group). ( I ) Representative western blots showing the UCP1 and PGC1α changes (n = 3/each group). ( J ) Continuous measurement of OCR in Ang-(1-7) and H89-treated primary brown Adipocytes (n = 3–5/each group). Data represent mean ± SEM. *p< 0.05, **p < 0.01 vs GFP/WT group by Student’s t -test. *p < 0.05, **p < 0.01 vs control group, # p < 0.05, ## p < 0.01 vs Ang-(1-7) group by one-way ANOVA. ( K ) Mechanisms involved in ACE2 pathway activation-induced improvement of BAT function.
    Western Blot Primary Antibodies Against P Akt308, 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/result/western blot primary antibodies against p akt308/product/Cell Signaling Technology Inc
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    Cell Signaling Technology Inc p akt308
    Knockdown of ET-1 blocked the PI3K/Akt pathway. Western blot was performed to detect the level of p-PI3K, PI3K, p-Akt473, <t>p-Akt308</t> and Akt in ECA109 cells. ***, P<0.001, compared with the control group; ### , P<0.001, compared with the si-ET-1 group.
    P Akt308, 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/result/p akt308/product/Cell Signaling Technology Inc
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    Cell Signaling Technology Inc phos akt308
    Knockdown of ET-1 blocked the PI3K/Akt pathway. Western blot was performed to detect the level of p-PI3K, PI3K, p-Akt473, <t>p-Akt308</t> and Akt in ECA109 cells. ***, P<0.001, compared with the control group; ### , P<0.001, compared with the si-ET-1 group.
    Phos Akt308, 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/result/phos akt308/product/Cell Signaling Technology Inc
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    Image Search Results


    Primary brown adipocytes were isolated, cultured, and treated with Ang-(1-7) (10 –6 M) for 24 hr, Akt inhibitor MK2206 (20 μM) for 24 hr, PKA inhibitor H89 (30 μM) for 24 hr, or adenylylcyclase inhibitor SQ-22536 (10 μM) for 24 hours. ( A, B ) Representative western blots showing the changes of p-Akt308 and Akt in BAT of Ace2 -/y ( A ) and Lepr db/db + Ace2 mice ( B ) exposure at 4 °C (n = 3/each group). ( C ) Representative western blots showing the Akt, UCP1 and forkhead box protein O 1 (FoxO1) Changes (n = 3/each group). ( D ) Relative mRNA levels of thermogenic and mitochondrial genes (n = 4–6/each group). ( E ) Continuous measurement of oxygen consumption rate (OCR) in Ang-(1-7) and MK2206 treated primary brown adipocytes. Oxygen consumption was performed under basal conditions, following the addition of oligomycin (1 μM), the pharmacological uncoupler FCCP (1 μM) or the Complex III and I inhibitor antimycin A and rotenone (0.5 μM) (n = 3–4/each group). ( F, G ) Representative western blots showing the p-PKA and PKA changes in BAT of Ace2 -/y ( F ) and Lepr db/db + Ace2 mice ( G ) exposure at 4 °C (n = 3/each group). ( H ) Relative mRNA levels of thermogenic and mitochondrial genes (n = 4–6/each group). ( I ) Representative western blots showing the UCP1 and PGC1α changes (n = 3/each group). ( J ) Continuous measurement of OCR in Ang-(1-7) and H89-treated primary brown Adipocytes (n = 3–5/each group). Data represent mean ± SEM. *p< 0.05, **p < 0.01 vs GFP/WT group by Student’s t -test. *p < 0.05, **p < 0.01 vs control group, # p < 0.05, ## p < 0.01 vs Ang-(1-7) group by one-way ANOVA. ( K ) Mechanisms involved in ACE2 pathway activation-induced improvement of BAT function.

    Journal: eLife

    Article Title: ACE2 pathway regulates thermogenesis and energy metabolism

    doi: 10.7554/eLife.72266

    Figure Lengend Snippet: Primary brown adipocytes were isolated, cultured, and treated with Ang-(1-7) (10 –6 M) for 24 hr, Akt inhibitor MK2206 (20 μM) for 24 hr, PKA inhibitor H89 (30 μM) for 24 hr, or adenylylcyclase inhibitor SQ-22536 (10 μM) for 24 hours. ( A, B ) Representative western blots showing the changes of p-Akt308 and Akt in BAT of Ace2 -/y ( A ) and Lepr db/db + Ace2 mice ( B ) exposure at 4 °C (n = 3/each group). ( C ) Representative western blots showing the Akt, UCP1 and forkhead box protein O 1 (FoxO1) Changes (n = 3/each group). ( D ) Relative mRNA levels of thermogenic and mitochondrial genes (n = 4–6/each group). ( E ) Continuous measurement of oxygen consumption rate (OCR) in Ang-(1-7) and MK2206 treated primary brown adipocytes. Oxygen consumption was performed under basal conditions, following the addition of oligomycin (1 μM), the pharmacological uncoupler FCCP (1 μM) or the Complex III and I inhibitor antimycin A and rotenone (0.5 μM) (n = 3–4/each group). ( F, G ) Representative western blots showing the p-PKA and PKA changes in BAT of Ace2 -/y ( F ) and Lepr db/db + Ace2 mice ( G ) exposure at 4 °C (n = 3/each group). ( H ) Relative mRNA levels of thermogenic and mitochondrial genes (n = 4–6/each group). ( I ) Representative western blots showing the UCP1 and PGC1α changes (n = 3/each group). ( J ) Continuous measurement of OCR in Ang-(1-7) and H89-treated primary brown Adipocytes (n = 3–5/each group). Data represent mean ± SEM. *p< 0.05, **p < 0.01 vs GFP/WT group by Student’s t -test. *p < 0.05, **p < 0.01 vs control group, # p < 0.05, ## p < 0.01 vs Ang-(1-7) group by one-way ANOVA. ( K ) Mechanisms involved in ACE2 pathway activation-induced improvement of BAT function.

    Article Snippet: Antibody , Anti-p-Akt308 (rabbit monoclonal) , Cell signaling , #13038 RRID: AB_2629447 , (1:1000).

    Techniques: Isolation, Cell Culture, Western Blot, Activation Assay

    Journal: eLife

    Article Title: ACE2 pathway regulates thermogenesis and energy metabolism

    doi: 10.7554/eLife.72266

    Figure Lengend Snippet:

    Article Snippet: Antibody , Anti-p-Akt308 (rabbit monoclonal) , Cell signaling , #13038 RRID: AB_2629447 , (1:1000).

    Techniques: Transfection, Construct, Sequencing, Software

    Knockdown of ET-1 blocked the PI3K/Akt pathway. Western blot was performed to detect the level of p-PI3K, PI3K, p-Akt473, p-Akt308 and Akt in ECA109 cells. ***, P<0.001, compared with the control group; ### , P<0.001, compared with the si-ET-1 group.

    Journal: Translational Cancer Research

    Article Title: ET-1 promotes the growth and metastasis of esophageal squamous cell carcinoma via activating PI3K/Akt pathway

    doi: 10.21037/tcr.2020.04.26

    Figure Lengend Snippet: Knockdown of ET-1 blocked the PI3K/Akt pathway. Western blot was performed to detect the level of p-PI3K, PI3K, p-Akt473, p-Akt308 and Akt in ECA109 cells. ***, P<0.001, compared with the control group; ### , P<0.001, compared with the si-ET-1 group.

    Article Snippet: The polyvinylidene fluoride (PVDF) membranes were incubated overnight at 4 °C with the primary antibodies ET-1 (1:1,000, #ab117529, Abcam, USA), p-PI3K (1:1,000, #17366, Cell Signaling Technology, USA), PI3K (1:1,000, #4249, Cell Signaling Technology, USA), p-Akt473 (1:2,000, #4060, Cell Signaling Technology, USA), p-Akt308 (1:1,000, #13038, Cell Signaling Technology, USA), Akt (1:1,000, #4685, Cell Signaling Technology, USA) and β-actin (1:1,000, #ab5694, Abcam, USA).

    Techniques: Western Blot