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TIMM8A 293T Cell Transient Overexpression Lysate(Denatured)

  • Catalog # : H00001678-T01
  • Visit Frequency :
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  • Specification
  • Transfected Cell Line:
  • 293T
  • Plasmid:
  • pCMV-TIMM8A full-length
  • Host:
  • Human
  • Theoretical MW (kDa):
  • 10.78
  • Quality Control Testing:
  • Transient overexpression cell lysate was tested with Anti-TIMM8A antibody (H00001678-B01) by Western Blots.
    Western Blot
    QC Testing of H00001678-T01
    Lane 1: TIMM8A transfected lysate ( 11 KDa)
    Lane 2: Non-transfected lysate.
    SDS-PAGE Gel
    QC Testing of H00001678-T01
    TIMM8A transfected lysate.
  • Storage Buffer:
  • 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
  • Storage Instruction:
  • Store at -80°C. Aliquot to avoid repeated freezing and thawing.
  • Applications
  • Western Blot
  • Application Image
  • Western Blot
  • Gene Information
  • Entrez GeneID:
  • 1678
  • Gene Name:
  • TIMM8A
  • Gene Alias:
  • DDP,DDP1,DFN1,MGC12262,MTS
  • Gene Description:
  • translocase of inner mitochondrial membrane 8 homolog A (yeast)
  • Gene Summary:
  • 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
  • Other Designations:
  • OTTHUMP00000023681,deafness/dystonia peptide,translocase of inner mitochondrial membrane 8 homolog A
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