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人PEX12(NM_000286)ORF克隆
人PEX12(NM_000286)ORF克隆
¥1300元
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  • 商品货号:F154122
  • accession:NM_000286
  • 基因别名:PEX12
  • 基因描述:Homo sapiens peroxisomal biogenesis factor 12 (PEX12), mRNA.
  • 载体:现货载体
  • CDS区长度:1080
  • 翻译后氨基酸长度:359
  • 基因简介:This gene belongs to the peroxin-12 family. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS). [provided by RefSeq, Oct 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