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akt inhibitors akt1 inhibitor  (Santa Cruz Biotechnology)


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    Santa Cruz Biotechnology akt inhibitors akt1 inhibitor
    Akt Inhibitors Akt1 Inhibitor, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 91/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/akt+pkb+inhibitor/BML-257/ppr0826283-70-0-6
    Average 91 stars, based on 4 article reviews
    akt inhibitors akt1 inhibitor - by Bioz Stars, 2026-10
    91/100 stars

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    Related Articles

    Injection:

    Article Title: Mechanism of retinal pericyte migration through Angiopoietin/Tie-2 signaling pathway on diabetic rats
    Article Snippet: Intravitreal Injection of Tie-2 Inhibitor, ERK1/2 Inhibitor, Akt/PKB Inhibitor and DMSO After the rats anesthetized with ketamine hydrochloride intraperitoneally and pontocaine eyedrop for eyes anesthesia, we gave intravitreal injection of sterilized solution of Tie-2 inhibitor (CAS 948557-43-5, santacruz biotech Inc.), 0.1 mm in phosphate buffer saline (PBS) with a concentration of 5% of dimethyl sulfoxide (DMSO)/5 μL. .. We performed intravitreal injection of ERK1/2 inhibitor (U0126, santacruz biotech), and Akt/PKB inhibitor (API-1, Torics, bioscience) with the same dose. ..

    Article Title: Mechanism of retinal pericyte migration through Angiopoietin/Tie-2 signaling pathway on diabetic rats
    Article Snippet: Total number of pericyte were count on 3 random area (400× magnification) using image analyzing system (BX-53; Olympus Opticals, Hamburg, Germany). .. Intravitreal Injection of Tie-2 Inhibitor, ERK1/2 Inhibitor, Akt/PKB Inhibitor and DMSO After the rats anesthetized with ketamine hydrochloride intraperitoneally and pontocaine eyedrop for eyes anesthesia, we gave intravitreal injection of sterilized solution of Tie-2 inhibitor (CAS 948557-43-5, santacruz biotech Inc.), 0.1 mm in phosphate buffer saline (PBS) with a concentration of 5% of dimethyl sulfoxide (DMSO)/5 μL. .. We performed intravitreal injection of ERK1/2 inhibitor (U0126, santacruz biotech), and Akt/PKB inhibitor (API-1, Torics, bioscience) with the same dose.

    Saline:

    Article Title: Mechanism of retinal pericyte migration through Angiopoietin/Tie-2 signaling pathway on diabetic rats
    Article Snippet: Total number of pericyte were count on 3 random area (400× magnification) using image analyzing system (BX-53; Olympus Opticals, Hamburg, Germany). .. Intravitreal Injection of Tie-2 Inhibitor, ERK1/2 Inhibitor, Akt/PKB Inhibitor and DMSO After the rats anesthetized with ketamine hydrochloride intraperitoneally and pontocaine eyedrop for eyes anesthesia, we gave intravitreal injection of sterilized solution of Tie-2 inhibitor (CAS 948557-43-5, santacruz biotech Inc.), 0.1 mm in phosphate buffer saline (PBS) with a concentration of 5% of dimethyl sulfoxide (DMSO)/5 μL. .. We performed intravitreal injection of ERK1/2 inhibitor (U0126, santacruz biotech), and Akt/PKB inhibitor (API-1, Torics, bioscience) with the same dose.

    Concentration Assay:

    Article Title: Mechanism of retinal pericyte migration through Angiopoietin/Tie-2 signaling pathway on diabetic rats
    Article Snippet: Total number of pericyte were count on 3 random area (400× magnification) using image analyzing system (BX-53; Olympus Opticals, Hamburg, Germany). .. Intravitreal Injection of Tie-2 Inhibitor, ERK1/2 Inhibitor, Akt/PKB Inhibitor and DMSO After the rats anesthetized with ketamine hydrochloride intraperitoneally and pontocaine eyedrop for eyes anesthesia, we gave intravitreal injection of sterilized solution of Tie-2 inhibitor (CAS 948557-43-5, santacruz biotech Inc.), 0.1 mm in phosphate buffer saline (PBS) with a concentration of 5% of dimethyl sulfoxide (DMSO)/5 μL. .. We performed intravitreal injection of ERK1/2 inhibitor (U0126, santacruz biotech), and Akt/PKB inhibitor (API-1, Torics, bioscience) with the same dose.



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    Fig. 2. PPI of targets and predicted binding patterns of critical targets. A. Critical targets were picked from all targets of active ingredients and diseases. The size of nodes is proportional to degree centrality by topology analysis. B. Heatmap of Molecular Docking Binding Energies between the 22 Active Components of Gastrodia Elata and Five Key Target Proteins <t>(AKT1,</t> CASP3, BCL2, EGFR2, and HSP90AA1). C. Docking of Gastrodin to AKT1. D. Docking of Gastrodin to CASP3. E. Docking of Gastrodin to BCL2. F. Docking of Gastrodin to EGFR2. G. Docking of Gastrodin to HSP90AA1.
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    Fig. 2. PPI of targets and predicted binding patterns of critical targets. A. Critical targets were picked from all targets of active ingredients and diseases. The size of nodes is proportional to degree centrality by topology analysis. B. Heatmap of Molecular Docking Binding Energies between the 22 Active Components of Gastrodia Elata and Five Key Target Proteins <t>(AKT1,</t> CASP3, BCL2, EGFR2, and HSP90AA1). C. Docking of Gastrodin to AKT1. D. Docking of Gastrodin to CASP3. E. Docking of Gastrodin to BCL2. F. Docking of Gastrodin to EGFR2. G. Docking of Gastrodin to HSP90AA1.
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    Fig. 2. PPI of targets and predicted binding patterns of critical targets. A. Critical targets were picked from all targets of active ingredients and diseases. The size of nodes is proportional to degree centrality by topology analysis. B. Heatmap of Molecular Docking Binding Energies between the 22 Active Components of Gastrodia Elata and Five Key Target Proteins <t>(AKT1,</t> CASP3, BCL2, EGFR2, and HSP90AA1). C. Docking of Gastrodin to AKT1. D. Docking of Gastrodin to CASP3. E. Docking of Gastrodin to BCL2. F. Docking of Gastrodin to EGFR2. G. Docking of Gastrodin to HSP90AA1.
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    Fig. 2. PPI of targets and predicted binding patterns of critical targets. A. Critical targets were picked from all targets of active ingredients and diseases. The size of nodes is proportional to degree centrality by topology analysis. B. Heatmap of Molecular Docking Binding Energies between the 22 Active Components of Gastrodia Elata and Five Key Target Proteins <t>(AKT1,</t> CASP3, BCL2, EGFR2, and HSP90AA1). C. Docking of Gastrodin to AKT1. D. Docking of Gastrodin to CASP3. E. Docking of Gastrodin to BCL2. F. Docking of Gastrodin to EGFR2. G. Docking of Gastrodin to HSP90AA1.
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    Fig. 2. PPI of targets and predicted binding patterns of critical targets. A. Critical targets were picked from all targets of active ingredients and diseases. The size of nodes is proportional to degree centrality by topology analysis. B. Heatmap of Molecular Docking Binding Energies between the 22 Active Components of Gastrodia Elata and Five Key Target Proteins <t>(AKT1,</t> CASP3, BCL2, EGFR2, and HSP90AA1). C. Docking of Gastrodin to AKT1. D. Docking of Gastrodin to CASP3. E. Docking of Gastrodin to BCL2. F. Docking of Gastrodin to EGFR2. G. Docking of Gastrodin to HSP90AA1.
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    Image Search Results


    Fig. 2. PPI of targets and predicted binding patterns of critical targets. A. Critical targets were picked from all targets of active ingredients and diseases. The size of nodes is proportional to degree centrality by topology analysis. B. Heatmap of Molecular Docking Binding Energies between the 22 Active Components of Gastrodia Elata and Five Key Target Proteins (AKT1, CASP3, BCL2, EGFR2, and HSP90AA1). C. Docking of Gastrodin to AKT1. D. Docking of Gastrodin to CASP3. E. Docking of Gastrodin to BCL2. F. Docking of Gastrodin to EGFR2. G. Docking of Gastrodin to HSP90AA1.

    Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

    Article Title: Mechanism of Gastrodin against neurotoxicity based on network pharmacology, molecular docking and experimental verification.

    doi: 10.1016/j.biopha.2024.117611

    Figure Lengend Snippet: Fig. 2. PPI of targets and predicted binding patterns of critical targets. A. Critical targets were picked from all targets of active ingredients and diseases. The size of nodes is proportional to degree centrality by topology analysis. B. Heatmap of Molecular Docking Binding Energies between the 22 Active Components of Gastrodia Elata and Five Key Target Proteins (AKT1, CASP3, BCL2, EGFR2, and HSP90AA1). C. Docking of Gastrodin to AKT1. D. Docking of Gastrodin to CASP3. E. Docking of Gastrodin to BCL2. F. Docking of Gastrodin to EGFR2. G. Docking of Gastrodin to HSP90AA1.

    Article Snippet: In a separate experiment, the AKT1 inhibitor AKT VIII (20 mg/kg, 612847–09–3, MCE, Shanghai, China) was injected into the mice 12 hours before surgery, followed by a second injection immediately after the surgery.

    Techniques: Binding Assay

    Fig. 3. Predicted binding patterns of critical targets. A.The expression of five core target proteins in the POCD model treated with Gastrodin was detected by WB. B-F. Panel A quantitative analysis of the corresponding proteins (n = 3). G. Protein levels of AKT1 treated with AKT VIII inhibitors by Western blot, and Western blot analysis (n = 3). H. Quantitative analysis of the RNA level of AKT1. Data for all results are expressed as mean ± SEM. **p < 0.01, ***p < 0.001.

    Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

    Article Title: Mechanism of Gastrodin against neurotoxicity based on network pharmacology, molecular docking and experimental verification.

    doi: 10.1016/j.biopha.2024.117611

    Figure Lengend Snippet: Fig. 3. Predicted binding patterns of critical targets. A.The expression of five core target proteins in the POCD model treated with Gastrodin was detected by WB. B-F. Panel A quantitative analysis of the corresponding proteins (n = 3). G. Protein levels of AKT1 treated with AKT VIII inhibitors by Western blot, and Western blot analysis (n = 3). H. Quantitative analysis of the RNA level of AKT1. Data for all results are expressed as mean ± SEM. **p < 0.01, ***p < 0.001.

    Article Snippet: In a separate experiment, the AKT1 inhibitor AKT VIII (20 mg/kg, 612847–09–3, MCE, Shanghai, China) was injected into the mice 12 hours before surgery, followed by a second injection immediately after the surgery.

    Techniques: Binding Assay, Expressing, Western Blot