eIF4A1 Monoclonal Antibody(M8), 50ul Vessels Mutations in PEX2 result in

Mutations in PEX2 result in one form of Zellweger syndrome and infantile Refsum disease

and functions as a calcium-dependent proton channel that may regulate redox-dependent processes in lymphocytes and spermatozoa

viruses and fungi

which implicated the role in neurodegenerative diseases

eIF4A1 Monoclonal Antibody(M8), 50ul Vessels Mutations in PEX2 result inATP dependent RNA helicase which is a subunit of the eIF4F complex involved in cap recognition and is required for mRNA binding to ribosome. In the current model of translation initiation, eIF4A unwinds RNA secondary structures in the 5' UTR of mRNAs which is necessary to allow efficient binding of the small ribosomal subunit, and subsequent scanning for the initiator codon.,similarity: Belongs to the DEAD box helicase family.,similarity: Belongs to