RTN4IP1抗体;RTN4IP1 Polyclonal A

Description 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. Specification Aliases:NIMP; OPA10 Swissprot:Q8WWV3 Host/Isotype:Rabbit IgG Antibody Type:Primary antibody Storage:Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. Species Reactivity:Human, Mouse Immunogen:Synthetic peptide of human RTN4IP1 Formulation:pH7.4 PBS, 0.05% NaN3, 40% Glycerol Application IHC:1/40-1/200 ELISA:1/5000-1/10000