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primary antibody against p ir β  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc primary antibody against p ir β
    Key materials and software.
    Primary Antibody Against P Ir β, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 462 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/primary antibody against p ir β/product/Cell Signaling Technology Inc
    Average 96 stars, based on 462 article reviews
    primary antibody against p ir β - by Bioz Stars, 2026-03
    96/100 stars

    Images

    1) Product Images from "A decrease in Flavonifractor plautii and its product, phytosphingosine, predisposes individuals with phlegm-dampness constitution to metabolic disorders"

    Article Title: A decrease in Flavonifractor plautii and its product, phytosphingosine, predisposes individuals with phlegm-dampness constitution to metabolic disorders

    Journal: Cell Discovery

    doi: 10.1038/s41421-025-00789-x

    Key materials and software.
    Figure Legend Snippet: Key materials and software.

    Techniques Used: Software, Recombinant, Luciferase, Reporter Gene Assay, Plasmid Preparation, Control, Transfection, Enzyme-linked Immunosorbent Assay, Staining



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    Image Search Results


    Key materials and software.

    Journal: Cell Discovery

    Article Title: A decrease in Flavonifractor plautii and its product, phytosphingosine, predisposes individuals with phlegm-dampness constitution to metabolic disorders

    doi: 10.1038/s41421-025-00789-x

    Figure Lengend Snippet: Key materials and software.

    Article Snippet: Primary antibody against p-IR-β , Cell Signaling Technology, Inc., Shanghai, China , #2381.

    Techniques: Software, Recombinant, Luciferase, Reporter Gene Assay, Plasmid Preparation, Control, Transfection, Enzyme-linked Immunosorbent Assay, Staining

    Effects of ginsenoside Rc on the insulin signaling pathway in HUVECs. The cells were treated with HG, with or without ginsenoside Rc (25 and 50 μM), for 24 h followed by insulin (100 nM) stimulation for 30 min. (A) Western blot analysis for p-IRS1 Tyr896 and p-IRS1 ser307 . (B) Western blot analysis for p-PI3K p85 Tyr607 , p-Akt Ser473 , and p-eNOS Ser1177 . Data were expressed as mean ± SD from three independent experiments. ## p < 0.01 compared with control and * p < 0.05 and ** p < 0.01 compared with HG.

    Journal: Frontiers in Pharmacology

    Article Title: Ginsenoside Rc Ameliorates Endothelial Insulin Resistance via Upregulation of Angiotensin-Converting Enzyme 2

    doi: 10.3389/fphar.2021.620524

    Figure Lengend Snippet: Effects of ginsenoside Rc on the insulin signaling pathway in HUVECs. The cells were treated with HG, with or without ginsenoside Rc (25 and 50 μM), for 24 h followed by insulin (100 nM) stimulation for 30 min. (A) Western blot analysis for p-IRS1 Tyr896 and p-IRS1 ser307 . (B) Western blot analysis for p-PI3K p85 Tyr607 , p-Akt Ser473 , and p-eNOS Ser1177 . Data were expressed as mean ± SD from three independent experiments. ## p < 0.01 compared with control and * p < 0.05 and ** p < 0.01 compared with HG.

    Article Snippet: Primary antibodies against p-IRS1 Ser307 , IRS1, PI3K p-85, p-Akt Ser473 , Akt, p-eNOS Ser1177 , eNOS, p-IKKβ Ser177/181 , p-IKKβ, p-JNK Thr183/Tyr185 , and JNK were purchased from Cell Signaling Technology (Danvers, MA, United States).

    Techniques: Western Blot, Control

    Effects of ginsenoside Rc with MLN-4760 on the insulin signaling pathway in HUVECs. The cells were treated with HG plus ginsenoside Rc (50 μM) with or without MLN-4760 (100 nM) for 24 h followed by insulin (100 nM) stimulation for 30 min. (A) Western blot analysis for p-IRS1 Tyr896 and p-IRS1 ser307 . (B) Western blot analysis for p-PI3K p85 Tyr607 , p-Akt Ser473 , and p-eNOS Ser1177 . Data were expressed as mean ± SD from three independent experiments. # p < 0.05 and ## p < 0.01 compared with control, * p < 0.05 and ** p < 0.01 compared with HG, and & p < 0.05 compared with HG + ginsenoside Rc.

    Journal: Frontiers in Pharmacology

    Article Title: Ginsenoside Rc Ameliorates Endothelial Insulin Resistance via Upregulation of Angiotensin-Converting Enzyme 2

    doi: 10.3389/fphar.2021.620524

    Figure Lengend Snippet: Effects of ginsenoside Rc with MLN-4760 on the insulin signaling pathway in HUVECs. The cells were treated with HG plus ginsenoside Rc (50 μM) with or without MLN-4760 (100 nM) for 24 h followed by insulin (100 nM) stimulation for 30 min. (A) Western blot analysis for p-IRS1 Tyr896 and p-IRS1 ser307 . (B) Western blot analysis for p-PI3K p85 Tyr607 , p-Akt Ser473 , and p-eNOS Ser1177 . Data were expressed as mean ± SD from three independent experiments. # p < 0.05 and ## p < 0.01 compared with control, * p < 0.05 and ** p < 0.01 compared with HG, and & p < 0.05 compared with HG + ginsenoside Rc.

    Article Snippet: Primary antibodies against p-IRS1 Ser307 , IRS1, PI3K p-85, p-Akt Ser473 , Akt, p-eNOS Ser1177 , eNOS, p-IKKβ Ser177/181 , p-IKKβ, p-JNK Thr183/Tyr185 , and JNK were purchased from Cell Signaling Technology (Danvers, MA, United States).

    Techniques: Western Blot, Control