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  • Anti-ATRX, clone 23C - 4008324

    Document Type:
    Certificate of Analysis
    Lot Number:
    4008324
    Product Catalog Number:
    MABE897
    Product Catalog Name:
    Anti-ATRX Antibody, clone 23C
  • Anti-ATRX, clone 23C - 3677707

    Document Type:
    Certificate of Analysis
    Lot Number:
    3677707
    Product Catalog Number:
    MABE897
    Product Catalog Name:
    Anti-ATRX Antibody, clone 23C
  • Anti-ATRX, clone 39f - 3471509

    Document Type:
    Certificate of Analysis
    Lot Number:
    3471509
    Product Catalog Number:
    MABE1798
    Product Catalog Name:
    Anti-ATRX Antibody, clone 39f
  • Anti-ATRX, clone 39f - 4203379

    Document Type:
    Certificate of Analysis
    Lot Number:
    4203379
    Product Catalog Number:
    MABE1798
    Product Catalog Name:
    Anti-ATRX Antibody, clone 39f
  • Anti-ATRX, clone 23C - 3270703

    Document Type:
    Certificate of Analysis
    Lot Number:
    3270703
    Product Catalog Number:
    MABE897
    Product Catalog Name:
    Anti-ATRX Antibody, clone 23C
  • Anti-ATRX, clone 39f - 3312988

    Document Type:
    Certificate of Analysis
    Lot Number:
    3312988
    Product Catalog Number:
    MABE1798
    Product Catalog Name:
    Anti-ATRX Antibody, clone 39f
  • Anti-ATRX, clone 39f -Q2818221

    Document Type:
    Certificate of Analysis
    Lot Number:
    Q2818221
    Product Catalog Number:
    MABE1798
    Product Catalog Name:
    Anti-ATRX Antibody, clone 39f
  • ATRX induction by mutant huntingtin via Cdx2 modulates heterochromatin condensation and pathology in Huntington's disease. 22240898

    Aberrant chromatin remodeling is involved in the pathogenesis of Huntington's disease (HD) but the mechanism is not known. Herein, we report that mutant huntingtin (mtHtt) induces the transcription of alpha thalassemia/mental retardation X linked (ATRX), an ATPase/helicase and SWI/SNF-like chromatin remodeling protein via Cdx-2 activation. ATRX expression was elevated in both a cell line model and transgenic model of HD, and Cdx-2 occupancy of the ATRX promoter was increased in HD. Induction of ATRX expanded the size of promyelocytic leukemia nuclear body (PML-NB) and increased trimethylation of H3K9 (H3K9me3) and condensation of pericentromeric heterochromatin, while knockdown of ATRX decreased PML-NB and H3K9me3 levels. Knockdown of ATRX/dXNP improved the hatch rate of fly embryos expressing mtHtt (Q127). ATRX/dXNP overexpression exacerbated eye degeneration of eye-specific mtHtt (Q127) expressing flies. Our findings suggest that transcriptional alteration of ATRX by mtHtt is involved in pericentromeric heterochromatin condensation and contributes to the pathogenesis of HD.
    Document Type:
    Reference
    Product Catalog Number:
    Multiple
    Product Catalog Name:
    Multiple
  • PML nuclear bodies are highly organised DNA-protein structures with a function in heterochromatin remodelling at the G2 phase. 16735446

    We have recently demonstrated that heterochromatin HP1 proteins are aberrantly distributed in lymphocytes of patients with immunodeficiency, centromeric instability and facial dysmorphy (ICF) syndrome. The three HP1 proteins accumulate in one giant body over the 1qh and 16qh juxtacentromeric heterochromatins, which are hypomethylated in ICF. The presence of PML (promyelocytic leukaemia) protein within this body suggests it to be a giant PML nuclear body (PML-NB). The structural integrity of PML-NBs is of major importance for normal cell functioning. Nevertheless, the structural organisation and the functions of these nuclear bodies remain unclear. Here, we take advantage of the large size of the giant body to demonstrate that it contains a core of satellite DNA with proteins being organised in ordered concentric layers forming a sphere around it. We extend these results to normal PML-NBs and propose a model for the general organisation of these structures at the G2 phase. Moreover, based on the presence of satellite DNA and the proteins HP1, BRCA1, ATRX and DAXX within the PML-NBs, we propose that these structures have a specific function: the re-establishment of the condensed heterochromatic state on late-replicated satellite DNA. Our findings that chromatin-remodelling proteins fail to accumulate around satellite DNA in PML-deficient NB4 cells support a central role for PML protein in this cellular function.
    Document Type:
    Reference
    Product Catalog Number:
    Multiple
    Product Catalog Name:
    Multiple