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Anti-TIMM8A Polyclonal Antibody - Biotin
Cat: K115388P - Biotin
Summary:
【Product name】:Anti-TIMM8A Polyclonal Antibody - Biotin 【Source】:Rabbit
【Isotype】:IgG 【Purification】:Affinity purification
【Gene ID】:1678 【Swiss Prot】:O60220
【Tested applications】:WB ELISA IHC ICC
【Recommended dilution】:WB 1:50-200. ELISA 1:100-1000. IHC 1:20-200. ICC 1:50-200. IF 1:50-200
【Immunogen】:Recombinant protein of human TIMM8A
【Public Immunogen Range】:1-98aa
【Storage】:Store at -20℃. Avoid freeze / thaw cycles.
Background:
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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