SGPL1 Rabbit Polyclonal Antibody, 50ul Cell Screening and Imaging These differences cause translation initiation

These differences cause translation initiation at a downstream AUG and result in a shorter protein (isoform b)

This gene encodes a member of a family of serine/threonine protein kinases that participate in cell cycle regulation

Mutations in this gene are associated with neurofibromatosis type II which is characterized by nervous system and skin tumors and ocular abnormalities

Mutations in this gene and H6PD (hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)) are the cause of cortisone reductase deficiency

tissue specificity:Abundant in adipose tissues

SGPL1 Rabbit Polyclonal Antibody, 50ul Cell Screening and Imaging These differences cause translation initiation