GCN2(Phospho Thr899) Polyclonal Antibody, 100ul Immune Repertoire Sequencing and is present only in

and is present only in striated muscles

It binds to vitamin D and its plasma metabolites and transports them to target tissues

Mutations in this gene cause arginine:glycine amidinotransferase deficiency| an inborn error of creatine synthesis characterized by mental retardation| language impairment| and behavioral disorders

Alternately spliced transcript variants have been observed for this gene

TGFA has been associated with many types of cancers

GCN2(Phospho Thr899) Polyclonal Antibody, 100ul Immune Repertoire Sequencing and is present only inThis gene encodes a member of a family of kinases that phosphorylate the alpha subunit of eukaryotic translation initiation factor 2 (EIF2), resulting in the downregulaton of protein synthesis. The encoded protein responds to amino acid deprivation by binding uncharged transfer RNAs. It may also be activated by glucose deprivation and viral infection. Mutations in this gene have been found in individuals suffering from autosomal recessive pulmonary