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, cognitive disability, and seizures. There is a pseudogene for this gene on chromosome 12. Alternative splicing results in multiple transcript variants.
应用类型
WB
免疫原
Recombinant protein encompassing a sequence within the center region of human RTN4IP1. The exact sequence is proprietary.
来源宿主
Rabbit
反应性
该RTN4IP1 抗体的反应性请参考该产品的说明书
保存建议
Keep as concentrated solution. Aliquot and store at -20C or below. Avoid multiple freeze-thaw cycles.
其他
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