AGFG1 Polyclonal Antibody, 20ul Pathway and Network Analysis Alternative splicing or deletion caused

Alternative splicing or deletion caused by a translocation event in this paternally-expressed region is responsible for Angelman syndrome or Prader-Willi syndrome due to parental imprint switch failure

Compatible with VT1

which is found in proteins involved in RAB GTPase signaling and vesicle trafficking

and other molecules containing terminal N-acetyl hexosamines

This gene encodes one of the catalytic subunits of protein kinase A| which exists as a tetrameric holoenzyme with two regulatory subunits and two catalytic subunits| in its inactive form

AGFG1 Polyclonal Antibody, 20ul Pathway and Network Analysis Alternative splicing or deletion causedThe protein encoded by this gene is related to nucleoporins a class of proteins that mediate nucleocytoplasmic transport. The encoded protein binds the activation domain of the human immunodeficiency virus Rev protein when Rev is assembled onto its RNA target and is required for the nuclear export of Rev directed RNAs. Multiple transcript variants encoding different isoforms have been found for this gene.