FOH1B Polyclonal Antibody, 50ul Live Cell Imaging May be involved in the

May be involved in the control of initiation of DNA replication through its interaction with NAKAP95

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

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encoded by the CLIC4 gene

FOH1B Polyclonal Antibody, 50ul Live Cell Imaging May be involved in theFOLH1B (Folate Hydrolase 1B) is a Protein Coding gene. Among its related pathways are Metabolism and Amino acid synthesis and interconversion (transamination). Has both folate hydrolase and N acetylated alpha linked acidic dipeptidase (NAALADase) activity. Exhibits a dipeptidyl peptidase IV type activity.