Learn More
TIMM8A, Mouse, Purified MaxPab™ Polyclonal Antibody, Abnova™
Mouse polyclonal antibody raised against a full-length human TIMM8A protein.
Brand: Abnova H00001678-B01P.50ug
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 70kDa heterohexamer. Alternative splicing results in multiple transcript variants encoding distinct isoforms
Sequence: MDSSSSSSAAGLGAVDPQLQHFIEVETQKQRFQQLVHQMTELCWEKCMDKPGPKLDSRAEACFVNCVERFIDTSQFILNRLEQTQKSKPVFSESLSDSpecifications
| TIMM8A | |
| Polyclonal | |
| Mouse polyclonal antibody raised against a full-length human TIMM8A protein. | |
| TIMM8A | |
| DDP/DDP1/DFN1/MGC12262/MTS | |
| Mouse | |
| Affinity chromatography | |
| RUO | |
| 1678 | |
| Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing. | |
| Purified |
| Immunofluorescence, Western Blot | |
| Unconjugated | |
| PBS with no preservative; pH 7.4 | |
| NM_004085 | |
| TIMM8A | |
| TIMM8A (NP_004076.1, 1 a.a. ∼ 97 a.a) full-length human protein. | |
| 50 μg | |
| Primary | |
| Human | |
| Antibody | |
| IgG |
Your input is important to us. Please complete this form to provide feedback related to the content on this product.