该FARS2 Polyclonal Antibody. This gene encodes a protein that transfers phenylalanine to its cognate tRNA. This protein localizes to the mitochondrion and plays a role in mitochondrial protein translation. Mutations in this gene can cause combined oxidative phosphorylation deficiency 14 (Alpers encephalopathy). Alternative splicing results in multiple transcript variants.
应用类型
WB
免疫原
Recombinant fusion protein of human FARS2 (NP_006558.1).
