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TMEM230 Antibody

  • 货号：
    CSB-PA003711GA01HU
  • 规格：
    ￥3,900
  • 其他：

产品详情

  • Uniprot No.：
    Q96A57
  • 基因名：
    TMEM230
  • 别名：
    TMEM230; C20orf30; HSPC274; UNQ2432/PRO4992; Transmembrane protein 230
  • 宿主：
    Rabbit
  • 反应种属：
    Human,Mouse,Rat
  • 免疫原：
    Human C20orf30
  • 免疫原种属：
    Homo sapiens (Human)
  • 抗体亚型：
    IgG
  • 纯化方式：
    Antigen Affinity purified
  • 浓度：
    It differs from different batches. Please contact us to confirm it.
  • 保存缓冲液：
    PBS with 0.02% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
  • 产品提供形式：
    Liquid
  • 应用范围：
    ELISA,WB
  • Protocols：
  • 储存条件：
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 货期：
    Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

产品评价

靶点详情

  • 功能：
    Involved in trafficking and recycling of synaptic vesicles.
  • 基因功能参考文献：
    1. Findings suggest that the incidence of pathogenic variations in TMEM230 is very low and, therefore, TMEM230 do not play a major role in familial and sporadic Parkinson's disease patients in southern Spanish population which can have important implication in clinical investigation. PMID: 29771939
    2. These results suggest that TMEM230 mutations are not a frequent cause of PD with AD inheritance in the Italian population. PMID: 28318986
    3. TMEM230 mutations are rare in Chinese patients with familial PD. PMID: 28038866
    4. This study suggest that mutations in TMEM230 are not a common cause of Parkinson's disease. PMID: 28090676
    5. the TMEM230 stop codon mutation is rare in Parkinson's disease and essential tremor patients from China, especially eastern China. PMID: 27869322
    6. Study did not detect any potential functional exonic TMEM230 variants in sporadic multiple system atrophy in a Han Chinese cohort. PMID: 28320143
    7. These results suggest that TMEM230 gene mutations may be rare in Chinese populations, and the variability of TMEM230 gene may not be a main factor for sporadic Parkinson's disease patients in Chinese Han populations. PMID: 28446760
    8. These findings identifying TMEM230 as a component of granulovacuolar degeneration and dystrophic neurites suggest TMEM230 dysregulation as a likely mechanism playing an important role in the pathogenesis of Alzheimer's Disease. PMID: 28527219
    9. The identification of TMEM230 mutations in Parkinson's disease is potentially an important finding. PMID: 28568905
    10. TMEM230 mutation might be a rare cause of Chinese familial and sporadic Parkinson's-disease patients. PMID: 28709721
    11. Mutation in TMEM230 gene is not associated with Parkinson's disease. PMID: 28766910
    12. TMEM230 mutation may not be a common genetic factor for Chinese familial and sporadic PD patients. PMID: 27814995
    13. No variants in the TMEM230 region were found associated with PD, age at onset, or cerebrospinal fluid alpha-synuclein levels PMID: 28457580
    14. Mutations in TMEM230 is associated to Parkinson's disease (PD). PMID: 27818000
    15. TMEM230 mutation is associated with Parkinson's disease. PMID: 27270108
    16. knockdown of another Parkinson's disease (PD) gene, LRRK2, which phosphorylates Rab8a, similarly impairs retromer trafficking, secretory autophagy and Golgi-derived vesicle secretion, thus demonstrating converging roles of two PD genes TMEM230 and LRRK2 on Rab8a function, and suggesting that retromer and secretory dysfunction play an important role in PD pathogenesis. PMID: 28115417

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  • 相关疾病：
    Parkinson disease (PARK)
  • 亚细胞定位：
    Membrane; Multi-pass membrane protein. Golgi apparatus, trans-Golgi network. Cytoplasmic vesicle, secretory vesicle, synaptic vesicle. Early endosome. Recycling endosome. Late endosome. Cytoplasmic vesicle, autophagosome.
  • 蛋白家族：
    TMEM134/TMEM230 family
  • 数据库链接：

    HGNC: 15876

    OMIM: 168600

    KEGG: hsa:29058

    STRING: 9606.ENSP00000341364

    UniGene: Hs.472024