Neurophysin I Polyclonal Antibody, 50ul Funnels A mutation in this gene

A mutation in this gene has been reported to be associated with hereditary spastic paraplegia| however the pathogenicity of the mutation| which may simply represent a polymorphism| is unclear

The encoded protein is activated by vascular endothelial growth factor and may regulate angiogenesis

The F1 complex consists of 5 different subunits (alpha

Shorter isoforms of this protein which lack the C-terminal HECT domain are therefore unlikely to bind E2 enzymes

This protein interacts with RING finger proteins

Neurophysin I Polyclonal Antibody, 50ul Funnels A mutation in this geneOXT encodes a precursor protein that is processed to produce oxytocin and neurophysin I. Oxytocin is a posterior pituitary hormone which is synthesized as an inactive precursor in the hypothalamus along with its carrier protein neurophysin I. Together with neurophysin, it is packaged into neurosecretory vesicles and transported axonally to the nerve endings in the neurohypophysis, where it is either stored or secreted into the bloodstream. The