PTPRE Polyclonal Antibody, 50ul Enzymes & Activity Assays Mutations in this gene cause

Mutations in this gene cause congenital adrenal hyperplasia

GPRC5B (G protein-coupled receptor class C group 5 member B) encodes a member of the type 3 G protein-coupled receptor family

Recruitment of this protein to the plasma membrane occurs in a lysophosphatidic acid (LPA)-dependent manner and it regulates LPA-induced cell migration

COMT is important in the metabolism of catechol drugs used in the treatment of hypertension

PTPRE Polyclonal Antibody, 50ul Enzymes & Activity Assays Mutations in this gene causeThe protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. Several alternatively spliced transcript variants of this gene have been reported, at least two of which encode a receptor type PTP that possesses a short extracellular domain, a single