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人 SPG11 (NM_001160227) cDNA克隆
人 SPG11 (NM_001160227) cDNA克隆
  • 商品货号:FC120534
  • 已售 4 件 | 评价 0 人次 | 关注度 321
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    • accession:NM_001160227
    • 基因别名:SPG11
    • 基因描述:Homo sapiens spastic paraplegia 11 (autosomal recessive) (SPG11), transcript variant 2, mRNA.
    • 载体:现货载体
    • CDS区长度:6993
    • 翻译后氨基酸长度:2330
    • TranscriptVariant:This variant (2) lacks two alternate in-frame exons in the 3' coding region, compared to variant 1. The resulting isoform (2) lacks an internal segment, compared to isoform 1.
    • 基因简介:The protein encoded by this gene is a potential transmembrane protein that is phosphorylated upon DNA damage. Defects in this gene are a cause of spastic paraplegia type 11 (SPG11). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]
    • 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