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HARS2 抗体

HARS2 适用: 人, 小鼠, 大鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7263809
发货至: 中国
  • 抗原 See all HARS2 抗体
    HARS2 (Histidyl-tRNA Synthetase 2, Mitochondrial (Putative) (HARS2))
    适用
    • 15
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    人, 小鼠, 大鼠
    宿主
    • 13
    • 2
    克隆类型
    • 14
    • 1
    多克隆
    标记
    • 9
    • 2
    • 2
    • 2
    This HARS2 antibody is un-conjugated
    应用范围
    • 12
    • 9
    • 4
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human HARS2 (NP_036340.1).
    亚型
    IgG
    Top Product
    Discover our top product HARS2 Primary Antibody
  • 应用备注
    WB 1:500-1:2000 IHC 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    HARS2 (Histidyl-tRNA Synthetase 2, Mitochondrial (Putative) (HARS2))
    别名
    HARS2 (HARS2 产品)
    别名
    HARSL antibody, HARSR antibody, HO3 antibody, PRLTS2 antibody, HARS2 antibody, 4631412B19Rik antibody, AI593507 antibody, Harsl antibody, DTD1 antibody, Hars2l antibody, RGD1308426 antibody, Zmat2 antibody, histidyl-tRNA synthetase 2, mitochondrial antibody, histidyl-tRNA synthetase 2 antibody, histidyl-tRNA synthetase-like antibody, HARS2 antibody, Hars2 antibody, LOC100635288 antibody
    背景
    Aminoacyl-tRNA synthetases are a class of enzymes that charge tRNAs with their cognate amino acids. The protein encoded by this gene is an enzyme belonging to the class II family of aminoacyl-tRNA synthetases. Functioning in the synthesis of histidyl-transfer RNA, the enzyme plays an accessory role in the regulation of protein biosynthesis. The gene is located in a head-to-head orientation with HARS on chromosome five, where the homologous genes likely share a bidirectional promoter. Mutations in this gene are associated with the pathogenesis of Perrault syndrome, which involves ovarian dysgenesis and sensorineural hearing loss. Alternative splicing results in multiple transcript variants of this gene.
    分子量

    Observed_MW: 50 kDa

    Calculated_MW: 54 kDa/56 kDa

    基因ID
    23438
    UniProt
    P49590
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