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人CLN6(NM_017882)ORF克隆
人CLN6(NM_017882)ORF克隆
¥1100元
会员等级价V
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  • 商品货号:F109522
  • accession:NM_017882
  • 基因别名:CLN6
  • 基因描述:Homo sapiens ceroid-lipofuscinosis, neuronal 6, late infantile, variant (CLN6), mRNA.
  • 载体: 现货载体
  • CDS区长度:936
  • 翻译后氨基酸长度:311
  • 基因简介:This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function. [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