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e2 ag0292 proteins  (Proteintech)


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    Structured Review

    Proteintech e2 ag0292 proteins
    E2 Ag0292 Proteins, supplied by Proteintech, used in various techniques. Bioz Stars score: 85/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ube2n/UBE2N+Fusion+Protein/10__1038_slash_s41418___026___01716___7-352-9-16
    Average 85 stars, based on 2 article reviews
    e2 ag0292 proteins - by Bioz Stars, 2026-09
    85/100 stars

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    Related Articles

    Incubation:

    Article Title: Urolithin A improves muscle strength, exercise performance, and biomarkers of mitochondrial health in a randomized trial in middle-aged adults
    Article Snippet: Membranes were stained with red Ponceau (Sigma, P7170) to stain total protein pool. .. The following primary antibodies were incubated overnight diluted in blocking buffer: UBE2N (SantaCruz, sc-376470, 1:3000), Tubulin (Proteintech, 10004185, 1:3000), phospho-Parkin S65 (Cell Signaling, #36866, 1:1000), Parkin (Cell Signaling, #4211, 1:1000), OXPHOS Antibody Cocktail (Abcam, ab110413, 1:2000), VDAC (Proteintech, 10866-1-AP, 1:1000). .. After washings, the secondary antibody (goat-anti-mouse, Azure, AC2115, 1:5000) was incubated for 30 min. Antibody reactions detection were imaged using the GE Healthcare, ImageQuant LAS 500.

    Blocking Assay:

    Article Title: Urolithin A improves muscle strength, exercise performance, and biomarkers of mitochondrial health in a randomized trial in middle-aged adults
    Article Snippet: Membranes were stained with red Ponceau (Sigma, P7170) to stain total protein pool. .. The following primary antibodies were incubated overnight diluted in blocking buffer: UBE2N (SantaCruz, sc-376470, 1:3000), Tubulin (Proteintech, 10004185, 1:3000), phospho-Parkin S65 (Cell Signaling, #36866, 1:1000), Parkin (Cell Signaling, #4211, 1:1000), OXPHOS Antibody Cocktail (Abcam, ab110413, 1:2000), VDAC (Proteintech, 10866-1-AP, 1:1000). .. After washings, the secondary antibody (goat-anti-mouse, Azure, AC2115, 1:5000) was incubated for 30 min. Antibody reactions detection were imaged using the GE Healthcare, ImageQuant LAS 500.



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    Image Search Results


    Context-dependent dual roles of the immunoproteasome in cancer. The immunoproteasome (IP) exerts divergent functions depending on tumor type and microenvironmental context. On the pro-tumor side (red), IP activity sustains chronic inflammation, promotes IL-17/LMP7-driven prostate cancer progression, maintains AML stemness (PSMB10, UBE2N), rewires epigenetic and metabolic programs (DNMT1/3B loss, MCL-1 survival), and supports immune evasion via the USP24–STAT3–PD1 axis. Conversely, in immunogenic contexts (green), IP enhances tumor suppression by broadening the immunopeptidome and unmasking neoantigens, promoting CD8 + T-cell responses, with PSMB9 acting as a tumor suppressor in melanoma, glutamate flux inhibition boosting antigenicity in CRC, and dual MCL-1/MEK inhibition restoring therapy sensitivity in TNBC/IBC. High IP expression aligns with favorable prognosis in melanoma, bladder cancer, and TNBC. Notably, IP is dispensable for leukemia infected-cell vaccine efficacy (exception). Collectively, these findings position the IP as a context-dependent regulator, balancing between tumor-promoting inflammation and antigen-driven immune surveillance.

    Journal: Frontiers in Oncology

    Article Title: Rewiring tumor visibility: The immunopeptidome as a dynamic interface between antigen processing, microenvironmental stress, and immune recognition

    doi: 10.3389/fonc.2025.1691719

    Figure Lengend Snippet: Context-dependent dual roles of the immunoproteasome in cancer. The immunoproteasome (IP) exerts divergent functions depending on tumor type and microenvironmental context. On the pro-tumor side (red), IP activity sustains chronic inflammation, promotes IL-17/LMP7-driven prostate cancer progression, maintains AML stemness (PSMB10, UBE2N), rewires epigenetic and metabolic programs (DNMT1/3B loss, MCL-1 survival), and supports immune evasion via the USP24–STAT3–PD1 axis. Conversely, in immunogenic contexts (green), IP enhances tumor suppression by broadening the immunopeptidome and unmasking neoantigens, promoting CD8 + T-cell responses, with PSMB9 acting as a tumor suppressor in melanoma, glutamate flux inhibition boosting antigenicity in CRC, and dual MCL-1/MEK inhibition restoring therapy sensitivity in TNBC/IBC. High IP expression aligns with favorable prognosis in melanoma, bladder cancer, and TNBC. Notably, IP is dispensable for leukemia infected-cell vaccine efficacy (exception). Collectively, these findings position the IP as a context-dependent regulator, balancing between tumor-promoting inflammation and antigen-driven immune surveillance.

    Article Snippet: AML – UBE2N and proteostasis , UBE2N stabilizes proteins via K63 ubiquitination; its inhibition triggers K48-linked degradation through immunoproteasome, suppressing AML. , UBE2N is a vulnerability in immunoproteasome-positive AML; inhibition may serve as therapeutic strategy. , ( ) .

    Techniques: Activity Assay, Immunopeptidomics, Inhibition, Expressing, Infection