TIMM8A Polyclonal Antibody | G-AB-06412

TIMM8A Polyclonal Antibody | G-AB-06412 | Gentaur Antibodies

Overview: 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.

Category Type: Polyclonal Antibody

Research Areas: Neuroscience, Signal Transduction

Synonyms: 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

Reactivity: Human, Mouse, Rat

Host: Rabbit

Isotype: IgG

Gene ID:

Accession #: BC006994

Clonality: Polyclonal

Immunogen: Fusion protein of human TIMM8A

Clone #:

Conjugation: Unconjugated

Swissprot: O60220

Santa Cruz:

Calculated MW:

Observed MW:

Concentration: 1.62 mg/mL

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

Purification method: Antigen affinity purification

Application: IHC, ELISA

Dilution: IHC 1:50-1:300, ELISA 1:5000-1:10000

Storage: Store at -20°C. Avoid freeze / thaw cycles.

TIMM8A Polyclonal Antibody DataSheet