PTPZeta Polyclonal Antibody, 20ul Pathway and Network Analysis Take the risk and elevate

Take the risk and elevate your research to new heights

simplifying the training process

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

This protein contains conserved DLG (asp-leu-gly) and ENIL (glu-asn-ile-leu) motifs

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

PTPZeta Polyclonal Antibody, 20ul Pathway and Network Analysis Take the risk and elevatePTPRZ1 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.