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Recombinant Human Ribosome-releasing factor 2, mitochondrial (GFM2)

ACP12662

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP12662 Target NameGFM2
Target SynonymsGFM2; EFG2; MSTP027; Ribosome-releasing factor 2; mitochondrial; RRF2mt; Elongation factor G 2; mitochondrial; EF-G2mt; mEF-G 2; Elongation factor G2; hEFG2FormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Protein LengthFull?Length 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 IDQ969S9
Background Information
  • Uniprot Id

    Q969S9

  • Target Species

    Human

  • Target Name

    GFM2

  • Target Full Name

    Ribosome-releasing factor 2, mitochondrial

  • Target Function

    Mitochondrial GTPase that mediates the disassembly of ribosomes from messenger RNA at the termination of mitochondrial protein biosynthesis. Acts in collaboration with MRRF. GTP hydrolysis follows the ribosome disassembly and probably occurs on the ribosome large subunit. Not involved in the GTP-dependent ribosomal translocation step during translation elongation.

  • Target Subcellular Location

    Mitochondrion.

  • Target Protein Families

    TRAFAC class translation factor GTPase superfamily, Classic translation factor GTPase family, EF-G/EF-2 subfamily

  • Target Tissue Specificity

    Widely expressed.

  • Target Synonyms

    GFM2; EFG2; MSTP027; Ribosome-releasing factor 2; mitochondrial; RRF2mt; Elongation factor G 2; mitochondrial; EF-G2mt; mEF-G 2; Elongation factor G2; hEFG2

  • Target Background

    Eukaryotes contain two protein translational systems, one in the cytoplasm and one in the mitochondria. Mitochondrial translation is crucial for maintaining mitochondrial function and mutations in this system lead to a breakdown in the respiratory chain-oxidative phosphorylation system and to impaired maintenance of mitochondrial DNA. This gene encodes one of the mitochondrial translation elongation factors, which is a GTPase that plays a role at the termination of mitochondrial translation by mediating the disassembly of ribosomes from messenger RNA . Its role in the regulation of normal mitochondrial function and in disease states attributed to mitochondrial dysfunction is not known. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

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