FOH1B Polyclonal Antibody, 50ul Live Cell Imaging 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

The encoded protein may be involved in amyotrophic lateral sclerosis and Parkinson's disease

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May be involved in regulation of gene expression at the post-transcriptional level or in ribosome biogenesis in cancer cells

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

FOH1B Polyclonal Antibody, 50ul Live Cell Imaging Alternative splicing or deletion causedFOLH1B (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.