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    蛋白激酶樣內質網激酶抗體
    • 產品貨號:
      BN41823R
    • 中文名稱:
      蛋白激酶樣內質網激酶抗體
    • 英文名稱:
      Rabbit anti-PERK Polyclonal antibody
    • 品牌:
      Biorigin
    • 貨號

      產品規格

      售價

      備注

    • BN41823R-50ul

      50ul

      ¥1486.00

      交叉反應:Human,Mouse,Rat 推薦應用:WB,IHC-P,IHC-F,IF,Flow-Cyt,ELISA

    • BN41823R-100ul

      100ul

      ¥2360.00

      交叉反應:Human,Mouse,Rat 推薦應用:WB,IHC-P,IHC-F,IF,Flow-Cyt,ELISA

    • BN41823R-200ul

      200ul

      ¥3490.00

      交叉反應:Human,Mouse,Rat 推薦應用:WB,IHC-P,IHC-F,IF,Flow-Cyt,ELISA

    產品描述

    英文名稱PERK
    中文名稱蛋白激酶樣內質網激酶抗體
    別    名DKFZp781H1925; E2AK3_HUMAN; EC 2.7.11.1; EIF2AK3; Eukaryotic translation initiation factor 2 alpha kinase 3; Eukaryotic translation initiation factor 2-alpha kinase 3; Heme regulated EIF2 alpha kinase; HRI; HsPEK; Pancreatic eIF2 alpha kinase; Pancreatic eIF2-alpha kinase; PEK; PRKR like endoplasmic reticulum kinase; PRKR-like endoplasmic reticulum kinase; WRS.  



    研究領域免疫學  染色質和核信號  信號轉導  新陳代謝  表觀遺傳學  
    抗體來源Rabbit
    克隆類型Polyclonal
    交叉反應Human, Mouse, Rat, 
    產品應用WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 Flow-Cyt=1μg/Test IF=1:100-500 (石蠟切片需做抗原修復)
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    分 子 量122kDa
    細胞定位細胞漿 
    性    狀Liquid
    濃    度1mg/ml
    免 疫 原KLH conjugated synthetic peptide derived from human PERK:1001-1116/1116 
    亞    型IgG
    純化方法affinity purified by Protein A
    儲 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
    保存條件Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
    PubMedPubMed
    產品介紹The protein encoded by this gene 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. 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, Jan 2010]

    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 (CCND1).

    Subunit:
    Forms dimers with HSPA5/BIP in resting cells. Oligomerizes in ER-stressed cells. Interacts with DNAJC3.

    Subcellular Location:
    Endoplasmic reticulum membrane; Single-pass type I membrane protein.

    Tissue Specificity:
    Ubiquitous. A high level expression is seen in secretory tissues.

    Post-translational modifications:
    Oligomerization of the N-terminal ER luminal domain by ER stress promotes PERK trans-autophosphorylation of the C-terminal cytoplasmic kinase domain at multiple residues including Thr-982 on the kinase activation loop. Autophosphorylated. Phosphorylated at Tyr-619 following endoplasmic reticulum stress, leading to activate its tyrosine-protein kinase activity. Dephosphorylated by PTPN1/TP1B, leading to inactivate its enzyme activity.
    N-glycosylated.
    ADP-ribosylated by PARP16 upon ER stress, which increases kinase activity.

    DISEASE:
    Wolcott-Rallison syndrome (WRS) [MIM:226980]: 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. Note=The disease is caused by mutations affecting the gene represented in this entry.

    Similarity:
    Belongs to the protein kinase superfamily. Ser/Thr protein kinase family. GCN2 subfamily.
    Contains 1 protein kinase domain.

    SWISS:
    Q9NZJ5

    Gene ID:
    9451

    Database links:

    Entrez Gene: 9451 Human

    Entrez Gene: 13666 Mouse

    Entrez Gene: 29702 Rat

    Omim: 604032 Human

    SwissProt: Q9NZJ5 Human

    SwissProt: Q9Z2B5 Mouse

    SwissProt: Q9Z1Z1 Rat

    Unigene: 591589 Human

    Unigene: 247167 Mouse

    Unigene: 24897 Rat




    Important Note:
    This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.


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