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Antigenic Specificity | TIMM8A |
Clone | polyclonal |
Host Species | Rabbit |
Reactive Species | human |
Isotype | n/a |
Format | antigen affinity purified |
Size | 10 µl |
Concentration | 1000 µg/ml |
Applications | IP |
Reviews / Ratings | If you have used this antibody, please help fellow researchers by submitting reviews to pAbmAbs and antYbuddY. |
Description | Rabbit anti-TIMM8A Antibody, Affinity Purified. 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)]. |
Immunogen | Epitope: between 1 and 50 |
Other Names | DDP1; translocase of inner mitochondrial membrane 8 homolog A; MTS; TIM8; X-linked deafness dystonia protein; DFN1; deafness dystonia protein 1; DDP; mitochondrial import inner membrane translocase subunit Tim8 A; deafness/dystonia peptide |
Gene, Accession # | Gene ID: 1678, Accession: NP_004076.1, UniProt: O60220 |
Catalog # | A303-999A-T |
Price | $121 |
Order / More Info | TIMM8A Antibody from FORTIS LIFE SCIENCES |
Product Specific References | n/a |