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PTPRZ1 encodes a member of the receptor protein tyrosine phosphatase family. Additionally we are shipping Protein tyrosine Phosphatase, Receptor-Type, Z Polypeptide 1 Proteins (5) and Protein tyrosine Phosphatase, Receptor-Type, Z Polypeptide 1 Kits (1) and many more products for this protein.
Showing 10 out of 57 products:
Human Monoclonal PTPRZ1 Primary Antibody for BI, IF - ABIN967798
Krueger, Saito: A human transmembrane protein-tyrosine-phosphatase, PTP zeta, is expressed in brain and has an N-terminal receptor domain homologous to carbonic anhydrases. in Proceedings of the National Academy of Sciences of the United States of America 1992
Show all 5 references for ABIN967798
Human Polyclonal PTPRZ1 Primary Antibody for ELISA, WB - ABIN1451529
Hillier, Fulton, Fulton, Graves, Pepin, Wagner-McPherson, Layman, Maas, Jaeger, Walker, Wylie, Sekhon, Becker, OLaughlin, Schaller, Fewell, Delehaunty, Miner, Nash, Cordes, Du, Sun, Edwards et al.: The DNA sequence of human chromosome 7. ... in Nature 2003
The Protein Tyrosine Phosphatase (show ACP1 Antibodies) Rptpzeta Suppresses Osteosarcoma Development in Trp53 (show TP53 Antibodies)-Heterozygous Mice
The Pleiotrophin (show PTN Antibodies)-induced inactivation of PTPRZ was considered to be the adaptive mechanism underlying CNS remyelination in vivo.
Abnormal glycosylation of RPTP-zeta/phosphacan is neural cell-specific and may play a role in congenital muscular dystrophies.
Ptprz plays a negative role in oligodendrocyte differentiation in early central nervous system (CNS) development and remyelination in demyelinating CNS diseases.
RPTPbeta/zeta is associated with molecular, cellular, behavioral and cognitive schizophrenia phenotypes.
Ptprz is necessary to maintain central nervous system axonal integrity in a demyelinating environment.
Loss of RPTPZ promotes prostate cancer metastasi.
spatial and temporal expression patterns of O-mannosylated forms of RPTPzeta/phosphacan and its hypoglycosylation are suggestive of a role in the neural phenotypes observed in Congenital muscular dystrophies
An understanding of the specific functional role for phosphacan in stem cell neurobiology will be important for the therapeutic facilitation of nervous tissue repair and regeneration.
PTPRZ has a role in oligodendrocyte survival and in recovery from demyelinating disease
PTPRZ1 is affected in a contiguous gene deletion syndrome
Confirm contribution of PTPRZ1, and especially PTPRQ, in CRC carcinogenesis and demonstrated that PTPRQ expression is correlated with KRAS mutation.
Results provide evidence that PTPRB (show PTPRB Antibodies) and PLCG1 (show PLCG1 Antibodies) mutations are driving events in a subset of secondary angiosarcomas.
Data indicate that enhanced MET oncoprotein RNA expression by fusion with receptor-type tyrosine-protein phosphatase zeta (PTPRZ1).
Data indicate that the fusion arose from translocation events involving introns 3 or 8 of protein tyrosine phosphatase, receptor-type, Z polypeptide 1 (PTPRZ1) and intron 1 of hepatocyte growth factor receptor MET.
Distinct domains of PTPRZ-B are differentially required for migration and proliferation of glioma cells, respectively.
High expression of PTP receptors R and Z1 was observed in all examined cases of colorectal carcinoma, adenoma and normal colon tissue in this study.
VE-PTP (show PTPRB Antibodies) activates TIE2 (show TEK Antibodies) and stabilizes retinal and choroidal blood vessels
Protein tyrosine phosphatase (show ACP1 Antibodies) zeta enhances proliferation by increasing beta-catenin (show CTNNB1 Antibodies) nuclear expression in VHL (show VHL Antibodies)-inactive human renal cell carcinoma (show MOK Antibodies) cells.
these results suggest that the polarized redistribution of VE-PTP (show PTPRB Antibodies) in response to shear stress plays an important role in the regulation of endothelial cells function by blood flow.
This gene encodes a member of the receptor protein tyrosine phosphatase family. Expression of this gene 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 this gene.
, receptor-type tyrosine-protein phosphatase zeta
, 3F8 chondroitin sulfate proteoglycan
, 3H1 keratan sulfate proteoglycan
, protein tyrosine phosphate, receptor type, Z
, protein tyrosine phosphatase, receptor type, beta polypeptide
, receptor-type tyrosine-protein phosphatase beta
, vascular endothelial protein tyrosine phosphatase
, protein tyrosine phosphatase, receptor-type, zeta polypeptide 1
, protein-tyrosine phosphatase receptor type Z polypeptide 2
, receptor-type tyrosine phosphatase beta/zeta
, PTP zeta