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人 ATRX (NM_000489) cDNA克隆
人 ATRX (NM_000489) cDNA克隆
  • 商品货号:FC156985
  • 已售 5 件 | 评价 0 人次 | 关注度 348
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    • accession:NM_000489
    • 基因别名:ATRX
    • 基因描述:Homo sapiens alpha thalassemia/mental retardation syndrome X-linked (ATRX), transcript variant 1, mRNA.
    • 载体:现货载体
    • CDS区长度:7479
    • 翻译后氨基酸长度:2492
    • TranscriptVariant:This variant (1) encodes the longest isoform (1).
    • 基因简介: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. [provided by RefSeq, Aug 2013]
    • 规格:10ul 质粒
    CDS区参考序列: 点击查看序列
    翻译后氨基酸参数序列: 点击查看序列