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Plxna2 encodes a member of the plexin-A family of semaphorin co-receptors. Additionally we are shipping Plexin A2 Kits (8) and Plexin A2 Proteins (5) and many more products for this protein.
Showing 10 out of 36 products:
Human Polyclonal Plxna2 Primary Antibody for WB - ABIN2783972
Budel, Shim, Feng, Zhao, Hisama, Strittmatter: No association between schizophrenia and polymorphisms of the PlexinA2 gene in Chinese Han Trios. in Schizophrenia research 2008
Show all 2 references for ABIN2783972
Sema6a (show SEMA6A Antibodies) and Plxna2 have roles in promoting eye vesicle cohesion through mediating spatially regulated repulsion within the developing zebrafish eye
Data indicate that plexin A1 (show PLXNA1 Antibodies)-4 (PLXNA1 (show PLXNA1 Antibodies)-4) mediation of neuroanatomical traits can be detected using in vivo neuroimaging techniques.
although plexin-A4 (show PLXNA4 Antibodies) overexpression restored Sema3A (show SEMA3A Antibodies) signaling in plexin-A1 (show PLXNA1 Antibodies)-silenced cells, it failed to restore Sema3B (show SEMA3B Antibodies) signaling in plexin-A2-silenced cells.
PLXNA2 upregulation contributes to TMPRSS2 (show TMPRSS2 Antibodies):ERG (show ERG Antibodies)-mediated enhancements of PC3c cell migration and invasion.
PLXNA2 has been identified as a new rare copy number variations gene for tetralogy of Fallot.
results of our study reveal that PlxnA2 has a pro-osteogenic function by modulating BMP2 (show BMP2 Antibodies) signaling
PLXNA2 polymorphisms show association with ankylosing spondylitis.
in vitro analysis of PLXNA2 revealed that the gene has higher expression in more aggressive breast cancer cell types.
An association is identified between variants in the PLXNA2 gene and schizophrenia in two collections of schizophrenia cases and controls. High-density SNP mapping showed that the region of association spans approximately 60 kb of the PLXNA2 gene.
results suggest that PLXNA2 may not play a major role in the development of schizophrenia in our Japanese sample
PLXNA2 confers a varying genetic risk for schizophrenia among different populations.
Plexin A2 is expressed in both On and Off starburst amacrine cell.
crystal structures of cognate complexes of the semaphorin-binding regions of plexins B1 and A2 with semaphorin ectodomains (human PLXNB1 (show PLXNB1 Antibodies)(1-2)-SEMA4D (show SEMA4D Antibodies)(ecto (show TRIM33 Antibodies)) and murine PlxnA2(1-4)-Sema6A (show SEMA6A Antibodies)(ecto (show TRIM33 Antibodies))), plus unliganded structures of PlxnA2(1-4) and Sema6A (show SEMA6A Antibodies)(ecto (show TRIM33 Antibodies))
crystal structures of the semaphorin 6A (Sema6A (show SEMA6A Antibodies)) receptor-binding fragment and the plexin A2 (PlxnA2) ligand-binding fragment in both their pre-signalling (that is, before binding) and signalling (after complex formation) states
This study demonstrated that Sema6B (show SEMA6B Antibodies), another class 6 transmembrane semaphorin, is expressed in CA3 (show CA3 Antibodies) and repels mossy fibers in a PlxnA4 (show PLXNA4 Antibodies)-dependent manner in vitro.
In plexin-A2-deficient mice many granule cells remained in the molecular layer; mouse chimera studies further suggested that plexin-A2 acts in a cell-autonomous manner.
mutations in GATA6 (show GATA6 Antibodies) are genetic causes of congenital heart diseases involving outflow tract defects, as a result of the disruption of the direct regulation of semaphorin 3C (show SEMA3C Antibodies)-plexin A2 signaling
This gene encodes a member of the plexin-A family of semaphorin co-receptors. Semaphorins are a large family of secreted or membrane-bound proteins that mediate repulsive effects on axon pathfinding during nervous system development. A subset of semaphorins are recognized by plexin-A/neuropilin transmembrane receptor complexes, triggering a cellular signal transduction cascade that leads to axon repulsion. This plexin-A family member is thought to transduce signals from semaphorin-3A and -3C.
, plexin A2
, plexin 2
, semaphorin receptor OCT
, transmembrane protein OCT
, plex 2