TIMM8A Antibody

Translocase of inner mitochondrial membrane 8 homolog A (TIMM8A) is a translocase involved in the import and insertion of hydrophobic membrane proteins from the cytoplasm into the mitochondrial inner membrane. The TIMM8A 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 the TIMM8A gene also cause Jensen syndrome; an X-linked disease with opticoacoustic nerve atrophy and muscle weakness. Along with TIMM13, TIMM8A forms a 70 kDa heterohexamer [taken from NCBI Entrez Gene (Gene ID: 1678)].
TIMM8A
translocase of inner mitochondrial membrane 8 homolog A (yeast)
Mitochondrial import inner membrane translocase subunit Tim8 A
:  DDP DDP1 deafness dystonia protein 1 deafness/dystonia peptide DFN1 MTS TIM8 translocase of inner mitochondrial membrane 8 (yeast) homolog A X-linked deafness dystonia protein
Product
Specifications
Ordering Information
Human
IP
Between 1 to 50
$339
$99