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WB analysis of various sample lysates using GTX32644 HARS2 antibody. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of various sample lysates using GTX32644 HARS2 antibody. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of various sample lysates using GTX32644 HARS2 antibody. Dilution : 1:1000 Loading : 25microg per lane

HARS2 antibody

GTX32644
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetHARS2
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Overview

  • Supplier
    GeneTex
  • Product Name
    HARS2 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500 - 1:2000. IHC-P: 1:50 - 1:200. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID23438
  • Target name
    HARS2
  • Target description
    histidyl-tRNA synthetase 2, mitochondrial
  • Target synonyms
    HARSL, HARSR, HO3, HisRS, PRLTS2, histidine--tRNA ligase, mitochondrial, HARS-related, histidine tRNA ligase 2, mitochondrial (putative), histidine translase, histidine-tRNA ligase homolog, histidyl-tRNA synthetase 2, mitochondrial (putative), histidyl-tRNA synthetase 2, mitochondrial, hisRS, probable histidine--tRNA ligase, mitochondrial, probable histidyl-tRNA synthetase, mitochondrial
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP49590
  • Protein Name
    Histidine--tRNA ligase, mitochondrial
  • Scientific Description
    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. [provided by RefSeq, Jul 2013]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203