TIMM8A Antibody from FORTIS LIFE SCIENCES

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Antigenic SpecificityTIMM8A
Clonepolyclonal
Host SpeciesRabbit
Reactive Specieshuman
Isotypen/a
Formatantigen affinity purified
Size10 µl
Concentration1000 µg/ml
ApplicationsIP
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DescriptionRabbit 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)].
ImmunogenEpitope: between 1 and 50
Other NamesDDP1; 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 InfoTIMM8A Antibody from FORTIS LIFE SCIENCES
Product Specific Referencesn/a
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