4E-BP1 Polyclonal Antibody, 100ul[BT-AP00037] Metabolic enzymes Mutations in this gene have

Mutations in this gene have been associated with Oguchi disease

Neprilysin is present on leukemic cells of pre-B phenotype

Defects in SAR1B are a cause of chylomicron retention disease (CMRD)

NRG3 has been shown to activate the tyrosine phosphorylation of its cognate receptor

Members of this family encode proteins containing a homeobox homology domain| proline rich region and Src-homology 3 (SH3) domain| and are components of the Abi/WAVE complex which regulates actin polymerization

4E-BP1 Polyclonal Antibody, 100ul[BT-AP00037] Metabolic enzymes Mutations in this gene haveEIF4EBP1 encodes one member of a family of translation repressor proteins. The protein directly interacts with eukaryotic translation initiation factor 4E (eIF4E), which is a limiting component of the multisubunit complex that recruits 40S ribosomal subunits to the 5' end of mRNAs. Interaction of this protein with eIF4E inhibits complex assembly and represses translation. This protein is phosphorylated in response to various signals including UV