该AFG3L2 Polyclonal Antibody. This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders.
应用类型
WB,IHC
免疫原
Recombinant fusion protein of human AFG3L2 (NP_006787.2).
