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人CLN6(NM_017882)ORF克隆
人CLN6(NM_017882)ORF克隆
  • 商品货号:FO111538
  • ¥1100元
    已售 3 件 | 评价 0 人次 | 关注度 335
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    • 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