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人PRPH2(NM_000322)ORF克隆
人PRPH2(NM_000322)ORF克隆
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  • 商品货号:F157087
  • accession:NM_000322
  • 基因别名:PRPH2
  • 基因描述:Homo sapiens peripherin 2 (retinal degeneration, slow) (PRPH2), mRNA.
  • 载体:现货载体
  • CDS区长度:1041
  • 翻译后氨基酸长度:346
  • 基因简介:The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein found in the outer segment of both rod and cone photoreceptor cells. It may function as an adhesion molecule involved in stabilization and compaction of outer segment disks or in the maintenance of the curvature of the rim. This protein is essential for disk morphogenesis. Defects in this gene are associated with both central and peripheral retinal degenerations. Some of the various phenotypically different disorders are autosomal dominant retinitis pigmentosa, progressive macular degeneration, macular dystrophy and retinitis pigmentosa digenic. [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