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人BBS2(NM_031885)ORF克隆
人BBS2(NM_031885)ORF克隆
  • 商品货号:FO115815
  • 已售 1 件 | 评价 0 人次 | 关注度 462
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    • accession:NM_031885
    • 基因别名:BBS2
    • 基因描述:Homo sapiens Bardet-Biedl syndrome 2 (BBS2), mRNA.
    • 载体: 现货载体
    • CDS区长度:2166
    • 翻译后氨基酸长度:721
    • 基因简介:This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and mental retardation. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene forms a multiprotein BBSome complex with six other BBS proteins.[provided by RefSeq, Jan 2009]
    • 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