该TUFM Polyclonal Antibody. This gene encodes a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. A pseudogene has been identified on chromosome 17.
应用类型
IHC,IF
免疫原
Recombinant fusion protein of human TUFM (NP_003312.3).
