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Abnova/ATRX recombinant monoclonal antibody, clone ATRX/2900R/1kit/RAB00607
  • Abnova/ATRX recombinant monoclonal antibody, clone ATRX/2900R/1kit/RAB00607

Abnova/ATRX recombinant monoclonal antibody, clone ATRX/2900R/1kit/RAB00607

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貨號: RAB00607
品牌: Abnova
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  • 詳情
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      • Specification
      • Product Description:
      • Recombinant rabbit monoclonal antibody raised against human ATRX.
      • Immunogen:
      • Recombinant protein corresponding to human ATRX.
      • Host:
      • Rabbit
      • Reactivity:
      • Human
      • Form:
      • Liquid
      • Purification:
      • Protein A/G purification
      • Isotype:
      • IgG
      • Recommend Usage:
      • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (1-2 ug/mL)The optimal working dilution should be determined by the end user.
      • Storage Buffer:
      • In 1 mg/mL PBS.
      • Storage Instruction:
      • Store at -20 to -80°C.
      • Datasheet:
      • PDF DownloadDownload
      • Applications
      • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
      • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
      • Immunohistochemical staining of human prostate carcinoma.
      • Application Image
      • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
      • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
      • enlarge
      • Gene Information
      • Entrez GeneID:
      • 546
      • Protein Accession#:
      • P46100
      • Gene Name:
      • ATRX
      • Gene Alias:
      • ATR2,MGC2094,MRXHF1,RAD54,RAD54L,SFM1,SHS,XH2,XNP,ZNF-HX
      • Gene Description:
      • alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S. cerevisiae)
      • Omim ID:
      • 300032, 300448, 301040, 309580
      • Gene Ontology:
      • Hyperlink
      • Gene Summary:
      • The protein encoded by this gene contains an ATPase/helicase domain, and thus it belongs to the SWI/SNF family of chromatin remodeling proteins. The mutations of 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. 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. Multiple alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq
      • Other Designations:
      • DNA dependent ATPase and helicase,OTTHUMP00000024265,OTTHUMP00000062079,X-linked nuclear protein,Zinc finger helicase,helicase 2, X-linked,transcriptional regulator ATRX
      • Related Disease
      • Breast cancer
      • Breast Neoplasms
      • Genetic Predisposition to Disease
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