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RASD2 encodes a Ras-related protein that enriched in striatum. Additionally we are shipping RASD Family, Member 2 Proteins (6) and many more products for this protein.
Showing 10 out of 83 products:
Human Polyclonal RASD2 Primary Antibody for EIA, IHC (p) - ABIN500889
Yamamoto, Irie, Asada, Mino, Mandai, Takai: Direct binding of the human homologue of the Drosophila disc large tumor suppressor gene to seven-pass transmembrane proteins, tumor endothelial marker 5 (TEM5), and a novel TEM5-like protein. in Oncogene 2004
Show all 5 references for ABIN500889
Human Polyclonal RASD2 Primary Antibody for EIA, IHC (p) - ABIN500891
Spano, Branchi, Rosica, Pirro, Riccio, Mithbaokar, Affuso, Arra, Campolongo, Terracciano, Macchia, Bernal, Alleva, Di Lauro: Rhes is involved in striatal function. in Molecular and cellular biology 2004
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Human Polyclonal RASD2 Primary Antibody for EIA, WB - ABIN954461
Hill, Goddard, Ladds, Davey: The cationic region of Rhes mediates its interactions with specific Gbeta subunits. in Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2009
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Human Polyclonal RASD2 Primary Antibody for ELISA, WB - ABIN1450860
St Croix, Rago, Velculescu, Traverso, Romans, Montgomery, Lal, Riggins, Lengauer, Vogelstein, Kinzler: Genes expressed in human tumor endothelium. in Science (New York, N.Y.) 2000
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Rhes influences striatal cAMP/PKA-dependent signaling and synaptic plasticity in a gender-sensitive fashion
Findings reveal that ras homolog enriched in striatum is localized also in striatal cholinergic interneurons and, most importantly, lack of this G-protein, significantly alters dopamine D2 receptor (show DRD2 Antibodies) modulation of striatal cholinergic excitability.
Rhes is reduced in the brains of Huntington's disease patients.
The findings of this study suggested that Rhes may play a crucial role in striatal iron homeostasis.
Rhes robustly binds the autophagy regulator Beclin-1 (show BECN1 Antibodies), decreasing its inhibitory interaction with Bcl-2 (show BCL2 Antibodies) independent of JNK-1 (show MAPK8 Antibodies) signaling.
The sequestering of Rhes through its binding to mutant huntingtin (show HTT Antibodies) may decrease the ability of Rhes to perform vital physiological functions in the striatum neurons of Huntington disease (show HTT Antibodies) patients. (Review)
Rhes is an imidazoline-regulated transcript in pancreatic beta-cells
Rhes can interfere with the functional activity of wt and mutated TSHr (show TSHR Antibodies) and with the respective hormone-stimulated cAMP production of FSHr (show FSHR Antibodies) and LHr (show LHCGR Antibodies).
The genes RASD2 might be vulnerability genes for neuropsychologically defined subgroups of schizophrenic patients.
The monomeric G proteins AGS1 (show TREX1 Antibodies) and Rhes selectively influence Galphai-dependent signaling to modulate N-type (CaV2.2 (show CACNA1B Antibodies)) calcium channels.
Study showed that both genetic deletion of Rhes and pharmacological blockade of mTORC1 significantly attenuate dyskinesia development by reducing the sensitization of striato-nigral medium-sized spiny neurons to levodopa
ectopic expression of Rhes in the cerebellum of N171-82Q mice, during the asymptomatic period led to an exacerbation of motor deficits, including loss of balance and motor incoordination with ataxia (show USP14 Antibodies)-like features
Brain Rhes expression is decreased in a mouse model of Huntington's disease.
Rhes is necessary for Akt (show AKT1 Antibodies) dephosphorylation by the striatal multi-protein complex
behavioral symptoms of HD are regulated by Rhes
This study demonstrated that Rhes-deleted mice are dramatically protected from neurotoxicity and motor dysfunction in a striatal-specific model of Huntington's disease elicited by 3-nitropropionic acid.
Ths results of this study indicted that Rhes physiologically binds to and activates mTOR (show FRAP1 Antibodies) in the striatum and L-DOPA-induced dyskinesia.
Rhes disruption affects selected behavioral competencies, including a gender-dependent increase in anxiety levels and a clear motor coordination deficit but no learning or memory impairment.
This gene encodes a Ras-related protein that enriched in striatum. The product of this gene binds to GTP and possesses intrinsic GTPase activity. The gene belongs to the Ras superfamily of small GTPases. The exact function of this gene is unknown, but most striatum-specific mRNAs characterized to date encode components of signal transduction cascades.
RASD family, member 2
, GTP-binding protein Rhes
, Ras homolog enriched in striatum
, tumor endothelial marker 2
, ras homolog enriched in striatum