PTPZeta Polyclonal Antibody, 20ul Pathway and Network Analysis It is an integral membrane

It is an integral membrane protein and plays an important role in inhibiting neurotransmission by binding to the benzodiazepine receptor and opening an integral chloride channel

Defects in this gene are a cause of macular corneal dystrophy (MCD)

) leading to the fusion of this gene and the FBLN1 gene is found in a complex type of synpolydactyly

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PTPZeta Polyclonal Antibody, 20ul Pathway and Network Analysis It is an integral membranePTPRZ1 encodes a member of the receptor protein tyrosine phosphatase family. Expression of PTPRZ1 is restricted to the central nervous system (CNS), and it may be involved in the regulation of specific developmental processes in the CNS. Alternatively spliced transcript variants encoding different isoforms have been described for PTPRZ1.