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3μg Human TIMM8A protein (GTX67355-pro) by SDS-PAGE under reducing condition and visualized by coomassie blue stain.
3μg Human TIMM8A protein (GTX67355-pro) by SDS-PAGE under reducing condition and visualized by coomassie blue stain.
3μg Human TIMM8A protein (GTX67355-pro) by SDS-PAGE under reducing condition and visualized by coomassie blue stain.

Human TIMM8A protein, His tag

GTX67355-PRO
GeneTex
Protein IDO60220
Product group Proteins / Signaling Molecules
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Overview

  • Supplier
    GeneTex
  • Product Name
    Human TIMM8A protein, His tag
  • Delivery Days Customer
    9
  • Certification
    Research Use Only
  • Concentration
    0.25 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID1678
  • Target name
    TIMM8A
  • Target description
    translocase of inner mitochondrial membrane 8A
  • Target synonyms
    DDP, DDP1, DFN1, MTS, TIM8, mitochondrial import inner membrane translocase subunit Tim8 A, X-linked deafness dystonia protein, deafness dystonia protein 1, deafness/dystonia peptide, translocase of inner mitochondrial membrane 8 homolog A
  • Protein IDO60220
  • Protein Name
    Mitochondrial import inner membrane translocase subunit Tim8 A
  • Scientific Description
    This translocase is involved in the import and insertion of hydrophobic membrane proteins from the cytoplasm into the mitochondrial inner membrane. The gene is mutated in Mohr-Tranebjaerg syndrome/Deafness Dystonia Syndrome (MTS/DDS) and it is postulated that MTS/DDS is a mitochondrial disease caused by a defective mitochondrial protein import system. Defects in this gene also cause Jensen syndrome; an X-linked disease with opticoacoustic nerve atrophy and muscle weakness. This protein, along with TIMM13, forms a 70 kDa heterohexamer. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Mar 2009]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    41116100
  • Species
    Human