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人OCRL(NM_001587)ORF克隆
人OCRL(NM_001587)ORF克隆
  • 商品货号:FO155150
  • 活动价: ¥2300元
    市场价:¥0元
    已售 3 件 | 评价 0 人次 | 关注度 664
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    • accession:NM_001587
    • 基因别名:OCRL
    • 基因描述:Homo sapiens oculocerebrorenal syndrome of Lowe (OCRL), transcript variant b, mRNA.
    • 载体:现货载体
    • CDS区长度:2682
    • 翻译后氨基酸长度:893
    • TranscriptVariant:This variant (2) lacks an alternate in-frame exon, compared to variant 1, resulting in a shorter protein (isoform 2) that has a shorter C-terminus, compared to isoform 1.
    • 基因简介:This gene encodes a phosphatase enzyme that is involved in actin polymerization and is found in the trans-Golgi network. Mutations in this gene cause oculocerebrorenal syndrome of Lowe and also Dent disease. [provided by RefSeq, Jul 2008]
    • 载体信息:自有图片地址
    • 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