SKU: E-AB-52670_20μL-ES

TIMM8A Polyclonal Antibody, 20 μL

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.

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Product Specification

Basic Information

Brands:Elabscience

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Place of Origin:China

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Shelf Life:12 months

Storage:Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.

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Dilution:IHC 1:50-1:300

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Application:IHC

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Research Areas:Neuroscience;Signal transduction

Species Reactivity:Human;Mouse;Rat

Reactivity:

Target Synonym:DDP 1;DDP;DDP1;Deafness dystonia protein 1;Deafness/dystonia peptide;DFN 1;DFN1;MGC12262;Mitochondrial import inner membrane translocase subunit Tim8 A;MTS;TIM 8A;TIM8;TIM8A;TIM8A;TIMM 8A;timm8a;Translocase of inner mitochondrial membrane 8 homolog A;X linked deafness dystonia protein;X-linked deafness dystonia protein

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Buffer:PBS with 0.05% NaN3 and 40% Glycerol,pH7.4

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