Background:

This gene encodes a mitochondrial protein that interacts with reticulon 4| which is a potent inhibitor of regeneration following spinal cord injury. This interaction may be important for reticulon-induced inhibition of neurite growth. Mutations in this gene can cause optic atrophy 10| with or without ataxia| mental retardation| and seizures. There is a pseudogene for this gene on chromosome 12. Alternative splicing results in multiple transcript variants.

Classification:

Primary antibody

Alternative names:

RT4I1

Species reactivity:

Human, Mouse

Host:

Rabbit

Isotype:

IgG

Immunogen:

Synthesized peptide derived from human RT4I1

Concentration:

1 mg/ml

Molecular weight:

43560

Applications:

WB

Storage:

-20°C for 1 year

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