- accession:NM_001276479
- 基因别名:LON; LONP; PIM1; hLON; LonHS; PRSS15
- 基因描述:Homo sapiens lon peptidase 1, mitochondrial (LONP1), transcript variant 2, mRNA.
- 载体:现货载体
- CDS区长度:2688
- 翻译后氨基酸长度:895
- TranscriptVariant:This variant (2) is alternatively spliced at the 5' end compared to variant 1. It uses the same translation start codon as variant 1, however, the encoded isoform (2) lacks a 64 aa protein segment in the 5' coding region compared to isoform 1.
- 基因简介:This gene encodes a mitochondrial matrix protein that belongs to the Lon family of ATP-dependent proteases. This protein mediates the selective degradation of misfolded, unassembled or oxidatively damaged polypeptides in the mitochondrial matrix. It may also have a chaperone function in the assembly of inner membrane protein complexes, and participate in the regulation of mitochondrial gene expression and maintenance of the integrity of the mitochondrial genome. Decreased expression of this gene has been noted in a patient with hereditary spastic paraplegia (PMID:18378094). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Feb 2013]
- 规格:10ul 质粒
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