FOH1B Polyclonal Antibody, 50ul Live Cell Imaging The protein is thought to

The protein is thought to play a role in cell-cell recognition during development of the central nervous system

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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

where it can also function as a receptor for human T-cell leukemia virus (HTLV) I and II

This complex translocates to the nucleus and activates the transcription of interferons alpha and beta

FOH1B Polyclonal Antibody, 50ul Live Cell Imaging The protein is thought toFOLH1B (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.