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ATRX Polyclonal Antibody

规格: / 20μL / 60μL / 120μL / 200μL
价格: / ¥420 / ¥1010 / ¥1640 / ¥2365

货号:E-AB-19609

宿主: Rabbit

反应性: H,M

应用: IHC

  • 详情
  • Overview

    Synonyms Alpha thalassemia/mental retardation syndrome X linked homolog,ATP dependent helicase ATRX,ATP-dependent helicase ATRX,ATR2,Atrx,ATRX,DNA dependent ATPase and helicase,Helicase 2, X linked,MGC2094,MRXHF1,RAD54,RAD54L,SFM1,SHS,Transcriptional regulator ATRX,X linked helicase II,X linked nuclear protein,X-linked helicase II,X-linked nuclear protein,XH2,XNP,Znf HX,Znf-HX,ATRX抗体
    Swissprot P46100
    Source Rabbit
    Reactivity Human, Mouse
    Immunogen Synthetic peptide of human ATRX
    Application IHC(Detection kit: E-IR-R213)
    Recommended dilution IHC,,1:30-1:150
    Concentration 0.7mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Nucleus. Chromosome, telomere. Nucleus, PML body. Associated with pericentromeric heterochromatin during interphase and mitosis, probably by interacting with CBX5/HP1 alpha. Colocalizes with histone H3.3, DAXX, HIRA and ASF1A at PML-nuclear bodies. Colocalizes with cohesin (SMC1 and SMC3) and MECP2 at the maternal H19 ICR (By similarity).
    Isotype IgG
    Purification Affinity purification
    Conjugation Unconjugated
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.05% NaN3 and 40% Glycerol,pH7.4
    Background The protein encoded by this gene contains an ATPase/helicase domain, and thus it belongs to the SWI/SNF family of chromatin remodeling proteins.This protein is found to undergo cell cycle-dependent phosphorylation, which regulates its nuclear matrix and chromatin association, and suggests its involvement in the gene regulation at interphase and chromosomal segregation in mitosis.Mutations in this gene are associated with an X-linked mental retardation (XLMR) syndrome most often accompanied by alpha-thalassemia (ATRX) syndrome.These mutations have been shown to cause diverse changes in the pattern of DNA methylation, which may provide a link between chromatin remodeling, DNA methylation, and gene expression in developmental processes.Multiple alternatively spliced transcript variants encoding distinct isoforms have been reported.
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