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Tu Translation Elongation Factor, Mitochondrial (Tufm) (Middle Region) Peptide

Tufm Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN985750
  • Target See all TUFM (Tufm) products
    TUFM (Tufm) (Tu Translation Elongation Factor, Mitochondrial (Tufm))
    Protein Region
    Middle Region
    Origin
    Human
    Source
    • 2
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Characteristics
    This is a synthetic peptide designed for use in combination with anti-TUFM antibody (Catalog #: ARP58546_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
    Purification
    Purified
  • Application Notes
    Each Investigator should determine their own optimal working dilution for specific applications.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Concentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handling Advice
    Avoid repeated freeze-thaw cycles.
    Storage
    -20 °C
    Storage Comment
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    TUFM (Tufm) (Tu Translation Elongation Factor, Mitochondrial (Tufm))
    Synonyms
    TUFM Peptide, D250 Peptide, fi06f04 Peptide, wu:fi06f04 Peptide, zgc:110766 Peptide, COXPD4 Peptide, EF-TuMT Peptide, EFTU Peptide, P43 Peptide, 2300002G02Rik Peptide, C76308 Peptide, C76389 Peptide, Tu translation elongation factor, mitochondrial Peptide, TUFM Peptide, tufm Peptide, Tufm Peptide
    Background
    TUFM is a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. This gene encodes a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. A pseudogene has been identified on chromosome 17. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

    Alias Symbols: COXPD4, EF-TuMT, EFTU, P43

    Protein Interaction Partner: ATP6V1A,MYH9,SGK1

    Protein Size: 455
    Molecular Weight
    50 kDa
    Gene ID
    7284
    NCBI Accession
    NM_003321, NP_003312
    UniProt
    P49411
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