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Recombinant Human Probable glutamate–tRNA ligase, mitochondrial (EARS2)

ACP17198

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP17198 Target NameEARS2
FormLyophilized powderExpression SystemCustom Production. Please inquire and provide the desire expression system.
Expression Range42-523Protein LengthFull Length of Mature Protein
Purity>85% (SDS-PAGE)Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDQ5JPH6
Background Information
  • Uniprot Id

    Q5JPH6

  • Target Species

    Human

  • Target Name

    EARS2

  • Target Full Name

    Nondiscriminating glutamyl-tRNA synthetase EARS2, mitochondrial

  • Target Function

    Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction: glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu).

  • Target Involvement

    Combined oxidative phosphorylation deficiency 12 (COXPD12)

  • Target Subcellular Location

    Mitochondrion matrix.

  • Target Protein Families

    Class-I aminoacyl-tRNA synthetase family, Glutamate--tRNA ligase type 1 subfamily

  • Target Synonyms

    3230401I01Rik; AL024049; COXPD12; EARS 2; ears2; GluRS; Glutamate--tRNA ligase; Glutamyl tRNA synthetase 2 mitochondrial; KIAA1970; mitochondrial; mKIAA1970; MSE1; Probable glutamyl tRNA synthetase; mitochondrial ; Probable glutamyl-tRNA synthetase; RGD1307904; SYEM_HUMAN

  • Target Background

    This gene encodes a member of the class I family of aminoacyl-tRNA synthetases. These enzymes play a critical role in protein biosynthesis by charging tRNAs with their cognate amino acids. This protein is encoded by the nuclear genome but is likely to be imported to the mitochondrion where it is thought to catalyze the ligation of glutamate to tRNA molecules. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency 12 (COXPD12). Alternative splicing results in multiple transcript variants.

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