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anti-Human PLEKHG5 Antikörper:
anti-Mouse (Murine) PLEKHG5 Antikörper:
anti-Rat (Rattus) PLEKHG5 Antikörper:
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Human Monoclonal PLEKHG5 Primary Antibody für IF, IHC (p) - ABIN566110
Ngok, Geyer, Liu, Kourtidis, Agrawal, Wu, Seerapu, Lewis-Tuffin, Moodie, Huveldt, Marx, Baraban, Storz, Horowitz, Anastasiadis: VEGF and Angiopoietin-1 exert opposing effects on cell junctions by regulating the Rho GEF Syx. in The Journal of cell biology 2012
Show all 2 Pubmed References
Results indicate that different mutations in PLEKHG5 lead to clinically diverse outcomes Charcot-Marie-Tooth disease or lower motor neuron disease affecting the function of neurons and glial cells.
Recruitment of Syx to the cell membrane, the selective activation of Dia1 signaling, coupled with the suppression of ROCK and actin reorganization, plays a key role in establishing cell polarity during directed cell migration.
This study identifies compound heterozygous PLEKHG5 mutations as the cause of recessive intermediate Charcot-Marie-Tooth disease.
a novel means of regulating junctional Syx localization and function by phosphorylation-induced 14-3-3 (zeige YWHAQ Antikörper) binding and further support the importance of Syx function in maintaining stable cell-cell contacts.
We identified a homozygous missense mutation (c.1940 T-->C [p.647 Phe-->Ser (zeige SIGLEC1 Antikörper)]) of the Pleckstrin (zeige PLEK Antikörper) homology domain-containing, family G member 5 gene (zeige GPD1 Antikörper), PLEKHG5, in families with lower motor neuron disease.
Plekhg5 affects cell polarity, migration, adhesion, degradation, and podosome organization in macrophages and osteoclasts.
VEGF (zeige VEGFA Antikörper) causes translocation of Syx from cell junctions, promoting junction disassembly, whereas angiopoietin 1 (zeige ANGPT1 Antikörper) maintains Syx at the junctions, inducing junction stabilization.
a well defined Rnd3 (zeige RND3 Antikörper) effector Syx
This gene encodes a protein that activates the nuclear factor kappa B (NFKB1) signaling pathway. Mutations in this gene are associated with autosomal recessive distal spinal muscular atrophy. Multiple transcript variants encoding different isoforms have been found for this gene.
pleckstrin homology domain containing, family G (with RhoGef domain) member 5
, pleckstrin homology domain containing family G member 5
, pleckstrin homology domain-containing family G member 5-like
, NFkB activating protein
, PH domain-containing family G member 5
, guanine nucleotide exchange factor 720
, novel PH domain-containing protein
, pleckstrin homology domain-containing family G member 5
, synectin-binding guanine exchange factor
, RhoA-specific guanine exchange factor SYX1
, RhoA-specific guanine exchange factor SYX2
, synectin-binding RhoA exchange factor
, neuronal RhoA GEF protein
, transcript highly enriched in cortex and hippocampus