PTPRK Polyclonal Antibody, 20ul Bottle-Top Dispenser disease:Defects in MT-ATP6 are a

disease:Defects in MT-ATP6 are a cause of infantile bilateral striatal necrosis

which is known as a precursor of the cornified cell envelope

13) involving this gene is associated with X-linked mental retardation

which catalyzes the release of large hydrophobic C-terminal amino acids

It is involved in many cellular functions

PTPRK Polyclonal Antibody, 20ul Bottle-Top Dispenser disease:Defects in MT-ATP6 are aThe 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. This PTP possesses an extracellular region, a single transmembrane region, and two tandem catalytic domains, and thus represents a receptor type PTP. The extracellular region contains a