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- accession：NM_001128834
- 基因别名：PLP1
- 基因描述：Homo sapiens proteolipid protein 1 (PLP1), transcript variant 3, mRNA.
- 载体：现货载体
- CDS区长度：834
- 翻译后氨基酸长度：277
- TranscriptVariant：This variant (3) contains an additional 5' non-coding exon, hence a longer 5' UTR, compared to transcript variant 1. Transcript variants 1 and 3 encode the same isoform (1).
- 基因简介：This gene encodes a transmembrane proteolipid protein that is the predominant myelin protein present in the central nervous system. It may play a role in the compaction, stabilization, and maintenance of myelin sheaths, as well as in oligodendrocyte development and axonal survival. Mutations in this gene cause X-linked Pelizaeus-Merzbacher disease and spastic paraplegia type 2. Alternatively spliced transcript variants encoding distinct isoforms or having different 5' UTRs, have been identified for this gene. [provided by RefSeq, Jul 2008]
- 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
