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26s proteasome inhibitor  (ApexBio)

 
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    ApexBio 26s proteasome inhibitor
    26s Proteasome Inhibitor, supplied by ApexBio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/26s proteasome inhibitor/product/ApexBio
    Average 90 stars, based on 1 article reviews
    26s proteasome inhibitor - by Bioz Stars, 2026-02
    90/100 stars

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    Quantitative analysis of the protein level of <t>26S</t> <t>proteasome</t> (PSMD2) in the PAG tissues. (A) The representative gel image shows the protein level of the PSMD2 in PAG tissues obtained from control (CON), KOA, and KOA treated with EA. β-actin was used as a loading control. The protein band at 100 kDa corresponds to the PSMD2. (B) Summary data show the effect of KOA and EA on the protein level of the PSMD2 in PAG tissues. Data are expressed as means ± SEM (n = 4 mice in each group). *** p < 0.001.
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    Quantitative analysis of the protein level of <t>26S</t> <t>proteasome</t> (PSMD2) in the PAG tissues. (A) The representative gel image shows the protein level of the PSMD2 in PAG tissues obtained from control (CON), KOA, and KOA treated with EA. β-actin was used as a loading control. The protein band at 100 kDa corresponds to the PSMD2. (B) Summary data show the effect of KOA and EA on the protein level of the PSMD2 in PAG tissues. Data are expressed as means ± SEM (n = 4 mice in each group). *** p < 0.001.
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    26s proteasome inhibitor mg132  (Beyotime)
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    Quantitative analysis of the protein level of <t>26S</t> <t>proteasome</t> (PSMD2) in the PAG tissues. (A) The representative gel image shows the protein level of the PSMD2 in PAG tissues obtained from control (CON), KOA, and KOA treated with EA. β-actin was used as a loading control. The protein band at 100 kDa corresponds to the PSMD2. (B) Summary data show the effect of KOA and EA on the protein level of the PSMD2 in PAG tissues. Data are expressed as means ± SEM (n = 4 mice in each group). *** p < 0.001.
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    Image Search Results


    Quantitative analysis of the protein level of 26S proteasome (PSMD2) in the PAG tissues. (A) The representative gel image shows the protein level of the PSMD2 in PAG tissues obtained from control (CON), KOA, and KOA treated with EA. β-actin was used as a loading control. The protein band at 100 kDa corresponds to the PSMD2. (B) Summary data show the effect of KOA and EA on the protein level of the PSMD2 in PAG tissues. Data are expressed as means ± SEM (n = 4 mice in each group). *** p < 0.001.

    Journal: Frontiers in Pharmacology

    Article Title: Hemoglobin α-derived peptides VD-hemopressin (α) and RVD-hemopressin (α) are involved in electroacupuncture inhibition of chronic pain

    doi: 10.3389/fphar.2024.1439448

    Figure Lengend Snippet: Quantitative analysis of the protein level of 26S proteasome (PSMD2) in the PAG tissues. (A) The representative gel image shows the protein level of the PSMD2 in PAG tissues obtained from control (CON), KOA, and KOA treated with EA. β-actin was used as a loading control. The protein band at 100 kDa corresponds to the PSMD2. (B) Summary data show the effect of KOA and EA on the protein level of the PSMD2 in PAG tissues. Data are expressed as means ± SEM (n = 4 mice in each group). *** p < 0.001.

    Article Snippet: MG132 (Z-Leu-Leu-Leu-al), a 26S proteasome inhibitor (Merck Millipore, United States) and AM251, a CB1 receptor selective antagonist (MCE, United States) were dissolved in the 10% dimethyl sulfoxide (10% DMSO; Sigma-Aldrich).

    Techniques: Control

    Effects of the 26S proteasome inhibitor MG132 on EA analgesia and RVD-hemopressin (α) concentration in the PAG. (A, B) Time course of the effect of the 26S proteasome inhibitor MG132 on tactile and thermal withdrawal thresholds of EA mice. EA was administered for 30 min, once every other day for 4 weeks, starting from 2 days after the MIA injection. The 26S proteasome inhibitor MG132 (4 μg) was microinjected into the vlPAG 30 min before EA starting from 18 days after MIA injection, once every other day for five times, as indicated by the black arrow. Data are expressed as means ± SEM (n = 8–11 mice in each group). * p < 0.05, compared with the KOA group; # p < 0.05, compared with the 10% DMSO + EA group. (C) Summary data show the concentration of RVD-hemopressin (α) in the PAG. Data are expressed as means ± SEM (n = 4–6 mice in each group). * p < 0.001.

    Journal: Frontiers in Pharmacology

    Article Title: Hemoglobin α-derived peptides VD-hemopressin (α) and RVD-hemopressin (α) are involved in electroacupuncture inhibition of chronic pain

    doi: 10.3389/fphar.2024.1439448

    Figure Lengend Snippet: Effects of the 26S proteasome inhibitor MG132 on EA analgesia and RVD-hemopressin (α) concentration in the PAG. (A, B) Time course of the effect of the 26S proteasome inhibitor MG132 on tactile and thermal withdrawal thresholds of EA mice. EA was administered for 30 min, once every other day for 4 weeks, starting from 2 days after the MIA injection. The 26S proteasome inhibitor MG132 (4 μg) was microinjected into the vlPAG 30 min before EA starting from 18 days after MIA injection, once every other day for five times, as indicated by the black arrow. Data are expressed as means ± SEM (n = 8–11 mice in each group). * p < 0.05, compared with the KOA group; # p < 0.05, compared with the 10% DMSO + EA group. (C) Summary data show the concentration of RVD-hemopressin (α) in the PAG. Data are expressed as means ± SEM (n = 4–6 mice in each group). * p < 0.001.

    Article Snippet: MG132 (Z-Leu-Leu-Leu-al), a 26S proteasome inhibitor (Merck Millipore, United States) and AM251, a CB1 receptor selective antagonist (MCE, United States) were dissolved in the 10% dimethyl sulfoxide (10% DMSO; Sigma-Aldrich).

    Techniques: Concentration Assay, Injection

    Effects of the 26S proteasome inhibitor MG132 on hemoglobin α-chain expression in the PAG. (A) The representative gel image shows the protein level of hemoglobin α-chain in PAG tissues obtained from CON, KOA, 10% DMSO + EA, and MG132 + EA groups. β-actin was used as a loading control. The protein band at 14 kDa corresponds to the hemoglobin α-chain. (B) Summary data show the effect of 26S proteasome inhibitor MG132 on the protein level of the hemoglobin α-chain in PAG tissues. EA was administered for 30 min, once every other day for 4 weeks, starting from 2 days after MIA injection. The 26S proteasome inhibitor MG132 (4 μg) was microinjected into the vlPAG 30 min before EA starting from 18 days after MIA injection, once every other day for five times. Data are expressed as means ± SEM (n = 3 mice in each group). * p < 0.05.

    Journal: Frontiers in Pharmacology

    Article Title: Hemoglobin α-derived peptides VD-hemopressin (α) and RVD-hemopressin (α) are involved in electroacupuncture inhibition of chronic pain

    doi: 10.3389/fphar.2024.1439448

    Figure Lengend Snippet: Effects of the 26S proteasome inhibitor MG132 on hemoglobin α-chain expression in the PAG. (A) The representative gel image shows the protein level of hemoglobin α-chain in PAG tissues obtained from CON, KOA, 10% DMSO + EA, and MG132 + EA groups. β-actin was used as a loading control. The protein band at 14 kDa corresponds to the hemoglobin α-chain. (B) Summary data show the effect of 26S proteasome inhibitor MG132 on the protein level of the hemoglobin α-chain in PAG tissues. EA was administered for 30 min, once every other day for 4 weeks, starting from 2 days after MIA injection. The 26S proteasome inhibitor MG132 (4 μg) was microinjected into the vlPAG 30 min before EA starting from 18 days after MIA injection, once every other day for five times. Data are expressed as means ± SEM (n = 3 mice in each group). * p < 0.05.

    Article Snippet: MG132 (Z-Leu-Leu-Leu-al), a 26S proteasome inhibitor (Merck Millipore, United States) and AM251, a CB1 receptor selective antagonist (MCE, United States) were dissolved in the 10% dimethyl sulfoxide (10% DMSO; Sigma-Aldrich).

    Techniques: Expressing, Control, Injection