Phospho-APC (S2054) Polyclonal Antibody, 100ul Cell Function Analysis possibly as a result of

possibly as a result of compromised regulatory T cell recruitment

it has been demonstrated that GALR2 couples efficiently to both the Gq and Gi proteins to simul

Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma

The type I isoform encoded by ARG1

Belongs to the alkB family

Phospho-APC (S2054) Polyclonal Antibody, 100ul Cell Function Analysis possibly as a result ofAPC encodes a tumor suppressor protein that acts as an antagonist of the Wnt signaling pathway. It is also involved in other processes including cell migration and adhesion, transcriptional activation, and apoptosis. Defects in this gene cause familial adenomatous polyposis (FAP), an autosomal dominant pre malignant disease that usually progresses to malignancy. Disease associated mutations tend to be clustered in a small region designated the