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HARS1/Jo-1 抗体 (C-Term)

HARS1 适用: 人 WB, ELISA, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7180180
发货至: 中国
  • 抗原 See all HARS1/Jo-1 (HARS1) 抗体
    HARS1/Jo-1 (HARS1) (Histidyl-tRNA Synthetase (HARS1))
    抗原表位
    • 15
    • 5
    • 5
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    C-Term
    适用
    • 41
    • 36
    • 8
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    宿主
    • 42
    • 8
    • 6
    克隆类型
    • 50
    • 5
    多克隆
    标记
    • 35
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This HARS1/Jo-1 antibody is un-conjugated
    应用范围
    • 43
    • 16
    • 14
    • 13
    • 13
    • 11
    • 10
    • 6
    • 5
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    Western Blotting (WB), ELISA, Immunofluorescence (IF)
    交叉反应
    人, 小鼠
    纯化方法
    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
    免疫原
    Synthesized peptide derived from C-terminal of Human HARS.
    亚型
    IgG
    Top Product
    Discover our top product HARS1 Primary Antibody
  • 应用备注
    WB:1:500-1:3000, IF:1:100-1:500,
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150 mM NaCl, 0.02 % sodium azide and 50 % glycerol.
    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,-80 °C
    储存方法
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 抗原
    HARS1/Jo-1 (HARS1) (Histidyl-tRNA Synthetase (HARS1))
    别名
    HARS (HARS1 产品)
    别名
    HRS antibody, USH3B antibody, MMHRS antibody, Dnd1 antibody, HARSL antibody, histidyl-tRNA synthetase antibody, HARS antibody, Hars antibody
    背景

    Background: Defects in HARS are a cause of Usher syndrome type 3B (USH3B). USH3B is a syndrome characterized by progressive vision and hearing loss during early childhood. Some patients have the so-called 'Charles Bonnet syndrome,' involving decreased visual acuity and vivid visual hallucinations. USH is a genetically heterogeneous condition characterized by the association of retinitis pigmentosa with sensorineural deafness. Age at onset and differences in auditory and vestibular function distinguish Usher syndrome type 1 (USH1), Usher syndrome type 2 (USH2) and Usher syndrome type 3 (USH3). USH3 is characterized by postlingual, progressive hearing loss, variable vestibular dysfunction, and onset of retinitis pigmentosa symptoms, including nyctalopia, constriction of the visual fields, and loss of central visual acuity, usually by the second decade of life. Belongs to the class-II aminoacyl-tRNA synthetase family.

    Raben N., Nucleic Acids Res. 20:1075-1081(1992).
    Tsui F.W.L., Nucleic Acids Res. 15:3349-3367(1987).
    Tsui H.W., Gene 131:201-208(1993).

    Aliases: cytoplasmic antibody, EC 6.1.1.21 antibody, FLJ20491 antibody, HARS antibody, HisRS antibody, Histidine tRNA ligase, cytoplasmic antibody, histidine translase antibody, Histidine tRNA ligase antibody, Histidine--tRNA ligase antibody, Histidyl tRNA synthetase antibody, Histidyl-tRNA synthetase antibody, HRS antibody, Human histidyl tRNA synthetase homolog (HO3) mRNA complete cds antibody, SYHC_HUMAN antibody, USH3B antibody

    UniProt
    P12081
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