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首页 > 产品中心 > 抗体系列 > 一抗

货号:BSCY0183

PERK Rabbit mAb

Eukaryotic translation initiation factor 2-alpha kinase 3 (PRKR-like endoplasmic reticulum kinase) (Pancreatic eIF2-alpha kinase) (HsPEK)

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别名 Eukaryotic translation initiation factor 2-alpha kinase 3 (PRKR-like endoplasmic reticulum kinase) (Pancreatic eIF2-alpha kinase) (HsPEK)
基因名称 Endogenous
蛋白名称 EIF2AK3
推荐应用
反应物种 PERK
存储缓冲液 WB 1:1000-1:5000;IF 1:200-1:1000;ELISA 1:5000-1:20000;
Human Gene Link EIF2AK3;PEK;PERK;Eukaryotic translation initiation factor 2-alpha kinase 3;PRKR-like endoplasmic reticulum kinase;Pancreatic eIF2-alpha kinase;HsPEK
Human Swissprot No. 9451
Mouse Gene ID Q9NZJ5
Rat Gene ID 29702
Rat Swissprot No. Q9Z1Z1
特异性 Monoclonal
稀释度 Unmodified
参考分子量 125kD
预测分子量 WB,IF,ELISA
运输及保存条件 Protein A
宿主 140kD
同种型 Rabbit
背景介绍 The protein encoded by this gene phosphorylates the alpha subunit of eukaryotic translation-initiation factor 2, leading to its inactivation, and thus to a rapid reduction of translational initiation and repression of global protein synthesis. This protein is thought to modulate mitochondrial function. It is a type I membrane protein located in the endoplasmic reticulum (ER), where it is induced by ER stress caused by malfolded proteins. Mutations in this gene are associated with Wolcott-Rallison syndrome. [provided by RefSeq, Sep 2015],
细胞定位 Endoplasmic reticulum membrane
功能 Catalytic activity:ATP + a protein = ADP + a phosphoprotein.,Disease:Defects in EIF2AK3 are the cause of Wolcott-Rallison syndrome (WRS) [MIM:226980]; also known as multiple epiphyseal dysplasia with early-onset diabetes mellitus. WRS is a rare autosomal recessive disorder, characterized by permanent neonatal or early infancy insulin-dependent diabetes and, at a later age, epiphyseal dysplasia, osteoporosis, growth retardation and other multisystem manifestations, such as hepatic and renal dysfunctions, mental retardation and cardiovascular abnormalities.,Domain:The lumenal domain senses perturbations in protein folding in the ER, probably through reversible interaction with HSPA5/BIP.,enzyme regulation:Perturbation in protein folding in the endoplasmic reticulum (ER) promotes reversible dissociation from HSPA5/BIP and oligomerization, resulting in transautophosphorylation and kinase activity induction.,Function:Phosphorylates the alpha subunit of eukaryotic translation-initiation factor 2 (EIF2), leading to its inactivation and thus to a rapid reduction of translational initiation and repression of global protein synthesis. Serves as a critical effector of unfolded protein response (UPR)-induced G1 growth arrest due to the loss of cyclin D1.,induction:By ER stress.,PTM:Autophosphorylated.,PTM:N-glycosylated.,similarity:Belongs to the protein kinase superfamily.,similarity:Belongs to the protein kinase superfamily. Ser/Thr protein kinase family. GCN2 subfamily.,similarity:Contains 1 protein kinase domain.,subunit:Forms dimers with HSPA5/BIP in resting cells. Oligomerizes in ER-stressed cells. Interacts with DNAJC3.,tissue specificity:Ubiquitous. A high level expression is seen in secretory tissues.,
纯化 PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
Clonality -15°C to -25°C/1 year(Do not lower than -25°C)
修饰类型 IgG,Kappa
细胞定位 Endoplasmic reticulum membrane
组织表达 Ubiquitous. A high level expression is seen in secretory tissues.

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