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VARS2 Antibody, HRP conjugated

  • 中文名稱:
    VARS2兔多克隆抗體, HRP偶聯
  • 貨號:
    CSB-PA735951LB01HU
  • 規格:
    ¥880
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) VARS2 Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    VARS2
  • 別名:
    COXPD20 antibody; mitochondrial antibody; SYVM_HUMAN antibody; Valine--tRNA ligase antibody; ValRS antibody; Valyl tRNA synthetase 2 mitochondrial antibody; Valyl-tRNA synthetase antibody; Valyl-tRNA synthetase-like antibody; Vars2 antibody; VARS2L antibody; VARSL antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Recombinant Human Valine--tRNA ligase, mitochondrial protein (830-981AA)
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標記方式:
    HRP
  • 克隆類型:
    Polyclonal
  • 抗體亞型:
    IgG
  • 純化方式:
    >95%, Protein G purified
  • 濃度:
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液:
    Preservative: 0.03% Proclin 300
    Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
  • 產品提供形式:
    Liquid
  • 應用范圍:
    ELISA
  • Protocols:
  • 儲存條件:
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 貨期:
    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.
  • 用途:
    For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產品評價

靶點詳情

  • 基因功能參考文獻:
    1. VARS2 mutation underlies a novel autosomal recessive syndrome with epilepsy, mental retardation, short stature, growth hormone deficiency, and hypogonadism. PMID: 29137650
    2. VARS2 polymorphism significantly associated with chronic hepatitis B in Korean population. PMID: 25404243
    3. VARS2 V552V may be considered as a prognostic factor for survival in patients with early breast cancer. PMID: 20503108
    4. Data indicate that variations in the levels of VARS2L between tissue types and patients could underlie the difference in clinical presentation between individuals homoplasmic for the 1624C>T MTTV (equivalent to mt-tRNAVal C25U) mutation. PMID: 18400783
  • 相關疾病:
    Combined oxidative phosphorylation deficiency 20 (COXPD20)
  • 亞細胞定位:
    Mitochondrion.
  • 蛋白家族:
    Class-I aminoacyl-tRNA synthetase family
  • 數據庫鏈接:

    HGNC: 21642

    OMIM: 612802

    KEGG: hsa:57176

    STRING: 9606.ENSP00000441000

    UniGene: Hs.597526



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