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

Interacts with the N-terminal part of PRKCI and PRKCZ

The protein has eleven transmembrane domains| an extracellular N-terminus and an intracellular C-terminal tail

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IL6R encodes a subunit of the interleukin 6 (IL6) receptor complex

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.