SYNM Rabbit Polyclonal Antibody, 100ul Antibody Humanization Mutation analysis of this gene

Mutation analysis of this gene has not revealed any mutation which causes the CPX disorder

The encoded protein is one of two functional homologs to yeast Upf3p

Its specific function is unknown

May be involved in up-regulation of the activity of kinases such as PKC via binding to KRT1

The first two N-terminal amino acids can be cleaved from human CCL4 by CD26/DPPIV

SYNM Rabbit Polyclonal Antibody, 100ul Antibody Humanization Mutation analysis of this geneThis gene encodes a putative member of the class II family of aminoacyl tRNA synthetases. These enzymes play a critical role in protein biosynthesis by charging tRNAs with their cognate amino acids. This protein is encoded by the nuclear genome but is likely to be imported to the mitochondrion where it is thought to catalyze the ligation of asparagine to tRNA molecules. Mutations in this gene have been associated with combined oxidative