人 PRF1 (NM_001083116) cDNA克隆

Accession: NM_001083116
基因名称: PRF1
基因别名: P1; PFP; FLH2; PFN1; HPLH2
基因描述: Homo sapiens perforin 1 (pore forming protein) (PRF1), transcript variant 2, mRNA.
种属: Human
CDS区长度: 1668 (查看编码区序列)
翻译后氨基酸长度: 555 (查看氨基酸序列)
Transcript Variant: This variant (2) differs in the 5' UTR compared to variant 1. Variants 1 and 2 encode the same protein.
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G117486 人 PRF1 (NM_001083116) cDNA克隆 pDONR223 2ug质粒 点击询价

The protein encoded by this gene has structural and functional similarities to complement component 9 (C9). Like C9, this protein creates transmembrane tubules and is capable of lysing non-specifically a variety of target cells. This protein is one of the main cytolytic proteins of cytolytic granules, and it is known to be a key effector molecule for T-cell- and natural killer-cell-mediated cytolysis. Defects in this gene cause familial hemophagocytic lymphohistiocytosis type 2 (HPLH2), a rare and lethal autosomal recessive disorder of early childhood. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]