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HARS2 Antibody

  • 货号：
    CSB-PA010138GA01HU
  • 规格：
    ￥3,900
  • 其他：

产品详情

  • Uniprot No.：
    P49590
  • 基因名：
    HARS2
  • 别名：
    4631412B19Rik antibody; AI593507 antibody; HARS related antibody; Hars2 antibody; HARSL antibody; HARSR antibody; HisRS antibody; Histidine translase antibody; Histidine tRNA ligase antibody; Histidine tRNA ligase homolog antibody; Histidine tRNA ligase like antibody; Histidine--tRNA ligase antibody; Histidine--tRNA ligase-like antibody; Histidyl tRNA synthetase 2 antibody; Histidyl tRNA synthetase 2 mitochondrial antibody; Histidyl tRNA synthetase like antibody; HO3 antibody; mitochondrial antibody; Probable histidyl tRNA synthetase mitochondrial antibody; Probable histidyl-tRNA synthetase antibody; SYHM_HUMAN antibody
  • 宿主：
    Rabbit
  • 反应种属：
    Human,Mouse,Rat
  • 免疫原：
    Human HARS2
  • 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,IHC
  • 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：
    Mitochondrial aminoacyl-tRNA synthetase that catalyzes the ATP-dependent ligation of histidine to the 3'-end of its cognate tRNA, via the formation of an aminoacyl-adenylate intermediate (His-AMP).
  • 基因功能参考文献：
    1. Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome. PMID: 21464306
    2. This protein has been found differentially expressed in the anterior cingulate cortex in men patients with schizophrenia. PMID: 20381070
  • 相关疾病：
    Perrault syndrome 2 (PRLTS2)
  • 亚细胞定位：
    Mitochondrion.
  • 蛋白家族：
    Class-II aminoacyl-tRNA synthetase family
  • 组织特异性：
    A high level expression is seen in the heart, kidney and skeletal muscle while a lower level expression is seen in the brain and liver.
  • 数据库链接：

    HGNC: 4817

    OMIM: 600783

    KEGG: hsa:23438

    STRING: 9606.ENSP00000230771

    UniGene: Hs.432560