Perforin 1 Polyclonal Antibody
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  • Perforin 1 Polyclonal Antibody

Perforin 1 Polyclonal Antibody


货       号:

YM-A21685

规       格:

50μL;100μL

种属反应:

Human,Rat,Mouse,

实验应用:

WB,IHC,ELISA

说明书:

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产品详情


产品名称

Perforin 1 Polyclonal Antibody

产品货号

YM-A21685

规格

50μL;100μL

种属反应

Human,Rat,Mouse,

实验应用

WB,IHC,ELISA

分子量

61kD

宿主

Rabbit

同种型

IgG

修饰

Unmodified

推荐稀释比

WB 1:500-2000;IHC 1:50-200;ELISA 1:10000-20000

组成

Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

纯化工艺

The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

储存

-15°C to -25°C/1 year(Do not lower than -25°C)

浓度

1 mg/ml

克降性

Polyclonal

克隆号

免疫原

The antiserum was produced against synthesized peptide derived from the C-terminal region of human PRF1. AA range:451-500

特异性

Perforin 1 Polyclonal Antibody detects endogenous levels of Perforin 1

基因名称

PRF1

蛋白名称

Perforin 1

别名

Perforin-1;P1;Cytolysin;Lymphocyte pore-forming protein;PFP;

基因ID-1

5551

SwissProt

P14222

背景

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],

细胞定位

Cytolytic granule . Secreted. Cell membrane ; Multi-pass membrane protein . Endosome lumen . Stored in cytolytic granules of cytolytic T-lymphocytes and secreted into the cleft between T-lymphocyte and target cell (PubMed:20038786). Inserts into the cell membrane of target cells and forms pores (PubMed:20889983). Membrane insertion and pore formation requires a major conformation change (PubMed:20889983). May be taken up via endocytosis involving clathrin-coated vesicles and accumulate in a first time in large early endosomes (PubMed:20038786). .

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