Trk A(Phospho Tyr757) Polyclonal Antibody, 50ul Purification Defects in this gene are

Defects in this gene are a cause of cytosolic phosphoenolpyruvate carboxykinase deficiency

1 Units/μL of yeast-based activity in a convenient 500 μL package

regulation of hormone secretion

CYP26B1 (cytochrome P450 family 26 subfamily B member 1) encodes a member of the cytochrome P450 superfamily

Trk A(Phospho Tyr757) Polyclonal Antibody, 50ul Purification Defects in this gene areThis gene encodes a member of the neurotrophic tyrosine kinase receptor (NTKR) family. This kinase is a membrane bound receptor that, upon neurotrophin binding, phosphorylates itself and members of the MAPK pathway. The presence of this kinase leads to cell differentiation and may play a role in specifying sensory neuron subtypes. Mutations in this gene have been associated with congenital insensitivity to pain, anhidrosis, self mutilating behavior,