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Human Arrestin 3 Protein expressed in Wheat germ - ABIN1345726
Quack, Woznowski, Potthoff, Palmer, Königshausen, Sivritas, Schiffer, Stegbauer, Vonend, Rump, Sellin: PKC alpha mediates beta-arrestin2-dependent nephrin endocytosis in hyperglycemia. in The Journal of biological chemistry 2011
Antihistamines displayed similar kinetic signatures on antagonizing histamine-induced beta-arrestin2 recruitment as compared to displacing radioligand binding from the H1R (zeige HRH1 Proteine).
the internalization motif for the human neuropeptide Y4 receptor, which regulates arrestin-3 recruitment and receptor endocytosis, was identified.
Collectively, these data show that beta-arrestin2 phosphorylation at Thr(383) underlies beta-arrestin-dependent Erk1/2 activation by G protein-coupled receptors.
Data indicate that a constitutively monomeric CXCL12 (zeige CXCL12 Proteine) variant reproduced the G protein-dependent and beta-arrestin-dependent responses that are associated with normal CXCR4 (zeige CXCR4 Proteine) signaling and lead to cell migration.
This work demonstrates that the expression of FSHR (zeige FSHR Proteine) and LHCGR (zeige LHCGR Proteine) can be induced in hGL5 cells but that the FSHR (zeige FSHR Proteine)-dependent cAMP/PKA pathway is constitutively silenced, possibly to protect cells from FSHR (zeige FSHR Proteine)-cAMP-PKA-induced apoptosis.
Lowering the level of cellular FLNA caused an elevation in RalA activity and resulted in selective interference with the normal intracellular trafficking and signaling of D3R through beta-arrestins.
This study reveals contrasting abilities of IGF-1R (zeige IGF1R Proteine) to interact with each b-arrestin (zeige SAG Proteine) isoform, depending on the presence of the ligand and demonstrates the antagonism between the two b-arrestin (zeige SAG Proteine) isoforms in controlling IGF-1R (zeige IGF1R Proteine) expression and function, which could be developed into a practical anti-IGF-1R (zeige IGF1R Proteine) strategy for cancer therapy.
Results demonstrate that GPR3 (zeige GPR3 Proteine) signals at the plasma membrane and can be silenced by GRK2 (zeige ADRBK1 Proteine)/beta-arrestin overexpression. These results also strongly implicate the serine and/or threonine residues in the third intracellular loop in the regulation of GPR3 (zeige GPR3 Proteine) activity.
EPCR (zeige PROCR Proteine) occupancy recruits G-protein coupled receptor kinase 5 (zeige GRK5 Proteine), thereby inducing beta-arrestin-2 biased PAR1 (zeige MARK2 Proteine) signaling by both APC (zeige APC Proteine) and thrombin (zeige F2 Proteine). In
CCR5 is highly expressed in active inflammatory bowel disease, and it has positive correlation with lymphocyte grade and negative correlation with expression of beta-arrestin2.
The fraction of arrestin2 molecules found in clusters larger than 100nm correlates with the magnitude of ligand-induced CCR5 internalization.
K2A mutations in arrestin-1 (zeige SAG Proteine), -2, and -3 significantly reduced their binding to active phosphorhodopsin.
Results reveal that multiple intramolecular interactions coordinately regulate arrestin2 interaction with clathrin, highlighting this interaction as a critical step in regulating receptor trafficking.
GIP stimulation induces a switch in GIPR recycling from a rapid endosomal to a slow trans-Golgi network (TGN) pathway. GPCR kinases and b-arrestin2 are required for this switch in recycling.
beta-arrestin2-biased negative modulators of mGlu5 (zeige GRM5 Proteine) offer significant advantages over first-generation inhibitors for the treatment of fragile X (zeige FMR1 Proteine) and related disorders.
selective inactivation of the GPCR (zeige GPBAR1 Proteine)-associated protein beta-arrestin 2 in hepatocytes of adult mice results in greatly increased hepatic GCGR (zeige GCGR Proteine) signaling, leading to striking deficits in glucose homeostasis
AT1R (zeige AGTRAP Proteine)-beta-arrestin-2 pathway signaling plays an important role in renal fibrosis.
These data suggest that one allele of arrestin-2 (zeige ARRB1 Proteine) is unable to support normal locomotor behavior due to signaling and/or developmental defects.
Beta-arrestin-2 with beta-arrestin-1 shared common mechanisms to suppress podocyte autophagy by negative regulation of ATG12-ATG5 conjugation.
[beta]-arrestin2 regulates intestinal mucosal inflammation under both homeostatic and colitic conditions. Its mode of action involves negative regulation of T-cell activation and its requirement for induction of regulatory T cells.
Results suggest that the antipruritic effects of kappa opioid receptor (zeige OPRK1 Proteine) agonists may not require betaarrestin2
that pro- and anti-inflammatory activities of beta-arrestin2 are determined by beta-arrestin2 ubiquitination and that changes in USP20 (zeige USP20 Proteine) expression and/or activity can therefore regulate inflammatory responses
This shows that mood stabilizers lamotrigine, lithium and valproate can exert behavioral effects in mice by disrupting the beta-arrestin 2-mediated regulation of Akt/GSK3 signaling by D2 dopamine receptors.
Arrb2 physically interacts with the beta subunit (zeige POLG Proteine) of trimeric G-proteins and Dishevelled (zeige DVL2 Proteine), the interaction between arrb2 and Dishevelled (zeige DVL2 Proteine) is promoted by the beta/gamma subunits of trimeric G-proteins.
results suggest that a functional interaction between beta-arrestin 2 and Smoothened may be critical to regulate hedgehog (zeige SHH Proteine) signaling in zebrafish development
Members of arrestin/beta-arrestin protein family are thought to participate in agonist-mediated desensitization of G-protein-coupled receptors and cause specific dampening of cellular responses to stimuli such as hormones, neurotransmitters, or sensory signals. Arrestin beta 2, like arrestin beta 1, was shown to inhibit beta-adrenergic receptor function in vitro. It is expressed at high levels in the central nervous system and may play a role in the regulation of synaptic receptors. Besides the brain, a cDNA for arrestin beta 2 was isolated from thyroid gland, and thus it may also be involved in hormone-specific desensitization of TSH receptors. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene.
arrestin beta 2
, arrestin, beta 2
, arrestin 2
, beta-Arrestin 2
, arrestin beta-2
, arrestin 3
, beta arr2
, beta-arrestin 2