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  4. Recombinant Human Periaxin (PRX), partial

Recombinant Human Periaxin (PRX), partial

  • 中文名稱：
    人PRX重組蛋白
  • 貨號：
    CSB-YP018833HU
  • 規格：
  • 來源：
    Yeast
  • 其他：
  • 中文名稱：
    人PRX重組蛋白
  • 貨號：
    CSB-EP018833HU
  • 規格：
  • 來源：
    E.coli
  • 其他：
  • 中文名稱：
    人PRX重組蛋白
  • 貨號：
    CSB-EP018833HU-B
  • 規格：
  • 來源：
    E.coli
  • 共軛：
    Avi-tag Biotinylated

    E. coli biotin ligase (BirA) is highly specific in covalently attaching biotin to the 15 amino acid AviTag peptide. This recombinant protein was biotinylated in vivo by AviTag-BirA technology, which method is BriA catalyzes amide linkage between the biotin and the specific lysine of the AviTag.

  • 其他：
  • 中文名稱：
    人PRX重組蛋白
  • 貨號：
    CSB-BP018833HU
  • 規格：
  • 來源：
    Baculovirus
  • 其他：
  • 中文名稱：
    人PRX重組蛋白
  • 貨號：
    CSB-MP018833HU
  • 規格：
  • 來源：
    Mammalian cell
  • 其他：

產品詳情

  • 純度：
    >85% (SDS-PAGE)
  • 基因名：
    PRX
  • Uniprot No.：
  • 別名：
    CMT4F; KIAA1620; Periaxin; PRAX_HUMAN; Prx
  • 種屬：
    Homo sapiens (Human)
  • 蛋白長度：
    Partial
  • 蛋白標簽：
    Tag?type?will?be?determined?during?the?manufacturing?process.
    The tag type will be determined during production process. If you have specified tag type, please tell us and we will develop the specified tag preferentially.
  • 產品提供形式：
    Lyophilized powder
    Note: We will preferentially ship the format that we have in stock, however, if you have any special requirement for the format, please remark your requirement when placing the order, we will prepare according to your demand.
  • 復溶：
    We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference.
  • 儲存條件：
    Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
  • 保質期：
    The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself.
    Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.
  • 貨期：
    Delivery time may differ from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
    Note: All of our proteins are default shipped with normal blue ice packs, if you request to ship with dry ice, please communicate with us in advance and extra fees will be charged.
  • 注意事項：
    Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week.
  • Datasheet ：
    Please contact us to get it.

產品評價

靶點詳情

  • 功能：
    Scaffolding protein that functions as part of a dystroglycan complex in Schwann cells, and as part of EZR and AHNAK-containing complexes in eye lens fiber cells. Required for the maintenance of the peripheral myelin sheath that is essential for normal transmission of nerve impulses and normal perception of sensory stimuli. Required for normal transport of MBP mRNA from the perinuclear to the paranodal regions. Required for normal remyelination after nerve injury. Required for normal elongation of Schwann cells and normal length of the internodes between the nodes of Ranvier. The demyelinated nodes of Ranvier permit saltatory transmission of nerve impulses; shorter internodes cause slower transmission of nerve impulses. Required for the formation of appositions between the abaxonal surface of the myelin sheath and the Schwann cell plasma membrane; the Schwann cell cytoplasm is restricted to regions between these appositions. Required for the formation of Cajal bands and of Schmidt-Lanterman incisures that correspond to short, cytoplasm-filled regions on myelinated nerves. Recruits DRP2 to the Schwann cell plasma membrane. Required for normal protein composition of the eye lens fiber cell plasma membrane and normal eye lens fiber cell morphology.
  • 基因功能參考文獻：
    1. The study identified a variant of periaxin in a Chinese family with congenital cataract by exome sequencing. PMID: 27081207
    2. results offer a possible mechanism to the formation of periaxin complexes, improvement of complex stability, and establishment of a link between the extracellular matrix and the cytoskeleton PMID: 26940996
    3. we were able to simplify this complex phenotype and identified a causative mutation (p.R1070*) in the gene periaxin (PRX), a gene previously shown to cause peripheral neuropathy (Dejerine-Sottas syndrome) when this mutation is present PMID: 26059842
    4. Study of the periaxin gene should be considered in patients with severe demyelinating neuropathy associated with early infantile scoliosis. PMID: 24011642
    5. a variation of clinical phenotypes for CMT4F caused by a novel, nonsense PRX mutation, was shown. PMID: 22847150
    6. Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes. PMID: 21741241
    7. In this review, periaxin protein is required for the maintenance of peripheral nerve myelin; however, patients with PRX mutations have early-onset autosomal recessive demyelinating Charcot-Marie-Tooth disease or Dejerine-Sottas neuropathy. PMID: 21079185
    8. novel mutation in vocal cord paralysis PMID: 19950375
    9. Results indicate a prominent sensory neuropathy resulting from periaxin gene mutations and suggests a role for the carboxyl terminal domain of the periaxin protein. PMID: 12112076
    10. Periaxin mutation causes early-onset but slow-progressive Charcot-Marie-Tooth disease PMID: 15197604
    11. S399fsX410 mutation in the PRX gene and its effects at the protein level, which was identified in an 8-year-old patient with early-onsetCharcot-Marie-Tooth type 4F disease. PMID: 16534116
    12. A PRX mutation in Japanese patients is presented. PMID: 16770524
    13. Data show that the mutations in the periaxin (PRX) gene is associated with early-onset demyelinating AR-CMT and severe sensory loss. PMID: 18504680

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  • 相關疾病：
    Dejerine-Sottas syndrome (DSS); Charcot-Marie-Tooth disease 4F (CMT4F)
  • 亞細胞定位：
    [Isoform 1]: Cell membrane; Peripheral membrane protein; Cytoplasmic side. Nucleus. Cytoplasm.; [Isoform 2]: Cytoplasm.; Cell membrane. Cell junction.
  • 蛋白家族：
    Periaxin family
  • 組織特異性：
    Detected in spinal cord. Isoform 1 and isoform 2 are found in sciatic nerve and Schwann cells.
  • 數據庫鏈接：

    HGNC: 13797

    OMIM: 145900

    KEGG: hsa:57716

    STRING: 9606.ENSP00000326018

    UniGene: Hs.205457



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