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phospho eif2α  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phospho eif2α
    Phospho Eif2α, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 13 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/phospho eif2α/product/Cell Signaling Technology Inc
    Average 93 stars, based on 13 article reviews
    phospho eif2α - by Bioz Stars, 2026-02
    93/100 stars

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    Comparing signaling pathways that regulate protein synthesis in gastrocnemius muscle of WT and MKO mice . WT and MKO mice were treated with or without DEX (10 mg/kg body weight) for 1 week. At the end of treatment, mice were IP injected with insulin (1 unit per kg body weight) or PBS for 10 min, and gastrocnemius muscle was isolated and processed for ELISA to monitor the phosphorylation status of ( A ) p70S6K at Thr389, ( B ) 4E-BP1 at Thr37/Ser46 and ( C ) <t>eIF2α</t> at Ser52. n = 3 to 6, significance was denoted as ∗ p ≤ 0.05. Error bars represent the SD. DEX, dexamethasone.
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    Comparing signaling pathways that regulate protein synthesis in gastrocnemius muscle of WT and MKO mice . WT and MKO mice were treated with or without DEX (10 mg/kg body weight) for 1 week. At the end of treatment, mice were IP injected with insulin (1 unit per kg body weight) or PBS for 10 min, and gastrocnemius muscle was isolated and processed for ELISA to monitor the phosphorylation status of ( A ) p70S6K at Thr389, ( B ) 4E-BP1 at Thr37/Ser46 and ( C ) <t>eIF2α</t> at Ser52. n = 3 to 6, significance was denoted as ∗ p ≤ 0.05. Error bars represent the SD. DEX, dexamethasone.
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    Comparing signaling pathways that regulate protein synthesis in gastrocnemius muscle of WT and MKO mice . WT and MKO mice were treated with or without DEX (10 mg/kg body weight) for 1 week. At the end of treatment, mice were IP injected with insulin (1 unit per kg body weight) or PBS for 10 min, and gastrocnemius muscle was isolated and processed for ELISA to monitor the phosphorylation status of ( A ) p70S6K at Thr389, ( B ) 4E-BP1 at Thr37/Ser46 and ( C ) <t>eIF2α</t> at Ser52. n = 3 to 6, significance was denoted as ∗ p ≤ 0.05. Error bars represent the SD. DEX, dexamethasone.
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    Cell Signaling Technology Inc phospho eif2α elisa relative total eif2α
    Figure 6. Comparing signaling pathways that regulate protein synthesis in gastrocnemius muscle of WT and MKO mice. WT and MKO mice were treated with or without DEX (10 mg/kg body weight) for 1 week. At the end of treatment, mice were IP injected with insulin (1 unit per kg body weight) or PBS for 10 min, and gastrocnemius muscle was isolated and processed for ELISA to monitor the phosphorylation status of (A) p70S6K at Thr389, (B) 4E-BP1 at Thr37/Ser46 and (C) <t>eIF2α</t> at Ser52. n = 3 to 6, significance was denoted as *p ≤0.05. Error bars represent the SD. DEX, dexamethasone.
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    Cell Signaling Technology Inc pathscan phospho eif2α sandwich elisa kit
    Figure 6. Comparing signaling pathways that regulate protein synthesis in gastrocnemius muscle of WT and MKO mice. WT and MKO mice were treated with or without DEX (10 mg/kg body weight) for 1 week. At the end of treatment, mice were IP injected with insulin (1 unit per kg body weight) or PBS for 10 min, and gastrocnemius muscle was isolated and processed for ELISA to monitor the phosphorylation status of (A) p70S6K at Thr389, (B) 4E-BP1 at Thr37/Ser46 and (C) <t>eIF2α</t> at Ser52. n = 3 to 6, significance was denoted as *p ≤0.05. Error bars represent the SD. DEX, dexamethasone.
    Pathscan Phospho Eif2α Sandwich Elisa Kit, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Cell Signaling Technology Inc pathscan phospho eif2α kit
    Figure 6. Comparing signaling pathways that regulate protein synthesis in gastrocnemius muscle of WT and MKO mice. WT and MKO mice were treated with or without DEX (10 mg/kg body weight) for 1 week. At the end of treatment, mice were IP injected with insulin (1 unit per kg body weight) or PBS for 10 min, and gastrocnemius muscle was isolated and processed for ELISA to monitor the phosphorylation status of (A) p70S6K at Thr389, (B) 4E-BP1 at Thr37/Ser46 and (C) <t>eIF2α</t> at Ser52. n = 3 to 6, significance was denoted as *p ≤0.05. Error bars represent the SD. DEX, dexamethasone.
    Pathscan Phospho Eif2α Kit, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/pathscan phospho eif2α kit/product/Cell Signaling Technology Inc
    Average 93 stars, based on 1 article reviews
    pathscan phospho eif2α kit - by Bioz Stars, 2026-02
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    Comparing signaling pathways that regulate protein synthesis in gastrocnemius muscle of WT and MKO mice . WT and MKO mice were treated with or without DEX (10 mg/kg body weight) for 1 week. At the end of treatment, mice were IP injected with insulin (1 unit per kg body weight) or PBS for 10 min, and gastrocnemius muscle was isolated and processed for ELISA to monitor the phosphorylation status of ( A ) p70S6K at Thr389, ( B ) 4E-BP1 at Thr37/Ser46 and ( C ) eIF2α at Ser52. n = 3 to 6, significance was denoted as ∗ p ≤ 0.05. Error bars represent the SD. DEX, dexamethasone.

    Journal: The Journal of Biological Chemistry

    Article Title: The role of striated muscle Pik3r1 in glucose and protein metabolism following chronic glucocorticoid exposure

    doi: 10.1016/j.jbc.2021.100395

    Figure Lengend Snippet: Comparing signaling pathways that regulate protein synthesis in gastrocnemius muscle of WT and MKO mice . WT and MKO mice were treated with or without DEX (10 mg/kg body weight) for 1 week. At the end of treatment, mice were IP injected with insulin (1 unit per kg body weight) or PBS for 10 min, and gastrocnemius muscle was isolated and processed for ELISA to monitor the phosphorylation status of ( A ) p70S6K at Thr389, ( B ) 4E-BP1 at Thr37/Ser46 and ( C ) eIF2α at Ser52. n = 3 to 6, significance was denoted as ∗ p ≤ 0.05. Error bars represent the SD. DEX, dexamethasone.

    Article Snippet: Relative total eIF2α and phosphorylated eIF2α levels were measured using the PathScan Phospho-eIF2α (Ser51) and total eIF2α Sandwich ELISA kits (Cell Signaling Technology, Catalog #7286 and Catalog #7952.)

    Techniques: Protein-Protein interactions, Injection, Isolation, Enzyme-linked Immunosorbent Assay, Phospho-proteomics

    Comparing signaling pathways that regulate protein synthesis in gastrocnemius muscle of WT and MKO mice . WT and MKO mice were treated with or without DEX (10 mg/kg body weight) for 1 week. At the end of treatment, mice were IP injected with insulin (1 unit per kg body weight) or PBS for 10 min, and gastrocnemius muscle was isolated and processed for ELISA to monitor the phosphorylation status of ( A ) p70S6K at Thr389, ( B ) 4E-BP1 at Thr37/Ser46 and ( C ) eIF2α at Ser52. n = 3 to 6, significance was denoted as ∗ p ≤ 0.05. Error bars represent the SD. DEX, dexamethasone.

    Journal: The Journal of Biological Chemistry

    Article Title: The role of striated muscle Pik3r1 in glucose and protein metabolism following chronic glucocorticoid exposure

    doi: 10.1016/j.jbc.2021.100395

    Figure Lengend Snippet: Comparing signaling pathways that regulate protein synthesis in gastrocnemius muscle of WT and MKO mice . WT and MKO mice were treated with or without DEX (10 mg/kg body weight) for 1 week. At the end of treatment, mice were IP injected with insulin (1 unit per kg body weight) or PBS for 10 min, and gastrocnemius muscle was isolated and processed for ELISA to monitor the phosphorylation status of ( A ) p70S6K at Thr389, ( B ) 4E-BP1 at Thr37/Ser46 and ( C ) eIF2α at Ser52. n = 3 to 6, significance was denoted as ∗ p ≤ 0.05. Error bars represent the SD. DEX, dexamethasone.

    Article Snippet: Relative total eIF2α and phosphorylated eIF2α levels were measured using the PathScan Phospho-eIF2α (Ser51) and total eIF2α Sandwich ELISA kits (Cell Signaling Technology, Catalog #7286 and Catalog #7952.)

    Techniques: Protein-Protein interactions, Injection, Isolation, Enzyme-linked Immunosorbent Assay, Phospho-proteomics

    Figure 6. Comparing signaling pathways that regulate protein synthesis in gastrocnemius muscle of WT and MKO mice. WT and MKO mice were treated with or without DEX (10 mg/kg body weight) for 1 week. At the end of treatment, mice were IP injected with insulin (1 unit per kg body weight) or PBS for 10 min, and gastrocnemius muscle was isolated and processed for ELISA to monitor the phosphorylation status of (A) p70S6K at Thr389, (B) 4E-BP1 at Thr37/Ser46 and (C) eIF2α at Ser52. n = 3 to 6, significance was denoted as *p ≤0.05. Error bars represent the SD. DEX, dexamethasone.

    Journal: Journal of Biological Chemistry

    Article Title: The role of striated muscle Pik3r1 in glucose and protein metabolism following chronic glucocorticoid exposure

    doi: 10.1016/j.jbc.2021.100395

    Figure Lengend Snippet: Figure 6. Comparing signaling pathways that regulate protein synthesis in gastrocnemius muscle of WT and MKO mice. WT and MKO mice were treated with or without DEX (10 mg/kg body weight) for 1 week. At the end of treatment, mice were IP injected with insulin (1 unit per kg body weight) or PBS for 10 min, and gastrocnemius muscle was isolated and processed for ELISA to monitor the phosphorylation status of (A) p70S6K at Thr389, (B) 4E-BP1 at Thr37/Ser46 and (C) eIF2α at Ser52. n = 3 to 6, significance was denoted as *p ≤0.05. Error bars represent the SD. DEX, dexamethasone.

    Article Snippet: All steps afterward were followed according to manufacturer’s instructions. eIF2α and phospho-eIF2α ELISA Relative total eIF2α and phosphorylated eIF2α levels were measured using the PathScan Phospho-eIF2α (Ser51) and total eIF2α Sandwich ELISA kits (Cell Signaling Technology, Catalog #7286 and Catalog #7952.)

    Techniques: Protein-Protein interactions, Injection, Isolation, Enzyme-linked Immunosorbent Assay, Phospho-proteomics