Arrestin-β-1 Polyclonal Antibody
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  • Arrestin-β-1 Polyclonal Antibody

Arrestin-β-1 Polyclonal Antibody


货       号:

YM-A17070

规       格:

50μL;100μL

种属反应:

Human,Monkey

实验应用:

WB,IHC,IF,ELISA

说明书:

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产品详情


产品名称

Arrestin-β-1 Polyclonal Antibody

产品货号

YM-A17070

规格

50μL;100μL

种属反应

Human,Monkey

实验应用

WB,IHC,IF,ELISA

分子量

47kD

宿主

Rabbit

同种型

IgG

修饰

Unmodified

推荐稀释比

WB 1:500-1:2000;IHC 1:100-1:300;IF 1:200-1:1000;ELISA 1:10000;Not yet tested in other applications.

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 human Arrestin 1. AA range:369-418

特异性

Arrestin-β-1 Polyclonal Antibody detects endogenous levels of Arrestin-β-1 protein.

基因名称

ARRB1

蛋白名称

Beta-arrestin-1

别名

ARRB1;ARR1;Beta-arrestin-1;Arrestin beta-1

基因ID-1

408

SwissProt

P49407

背景

Members of arrestin/beta-arrestin protein family are thought to participate in agonist-mediated desensitization of G-protein-coupled receptors and cause specific dampening of cellular responses to stimuli such as hormones, neurotransmitters, or sensory signals. Arrestin beta 1 is a cytosolic protein and acts as a cofactor in the beta-adrenergic receptor kinase (BARK) mediated desensitization of beta-adrenergic receptors. Besides the central nervous system, it is expressed at high levels in peripheral blood leukocytes, and thus the BARK/beta-arrestin system is believed to play a major role in regulating receptor-mediated immune functions. Alternatively spliced transcripts encoding different isoforms of arrestin beta 1 have been described. [provided by RefSeq, Jan 2011],

细胞定位

Cytoplasm. Nucleus. Cell membrane. Membrane, clathrin-coated pit . Cell projection, pseudopodium . Cytoplasmic vesicle. Translocates to the plasma membrane and colocalizes with antagonist-stimulated GPCRs. The monomeric form is predominantly located in the nucleus. The oligomeric form is located in the cytoplasm. Translocates to the nucleus upon stimulation of OPRD1 (By similarity). .

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