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anti-Human GRIA4 Antikörper:
anti-Rat (Rattus) GRIA4 Antikörper:
anti-Mouse (Murine) GRIA4 Antikörper:
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Human Polyclonal GRIA4 Primary Antibody für IHC (p), WB - ABIN656865
Muntané, Horvath, Hof, Ely, Hopkins, Raghanti, Lewandowski, Wray, Sherwood: Analysis of synaptic gene expression in the neocortex of primates reveals evolutionary changes in glutamatergic neurotransmission. in Cerebral cortex (New York, N.Y. : 1991) 2015
Human Polyclonal GRIA4 Primary Antibody für IHC (p), IHC - ABIN314841
Earnshaw, Bressloff: Biophysical model of AMPA receptor trafficking and its regulation during long-term potentiation/long-term depression. in The Journal of neuroscience : the official journal of the Society for Neuroscience 2006
The authors suggest that pathogenic de novo variants in GRIA4 lead to intellectual disability with or without seizures, gait abnormalities, problems of social behavior, and other variable features.
Study shows that alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor subunit GluA4 is expressed on oligodendrocytes, myelin and on axons in humans.
A transient positive feedback mechanism between AMPAR and stargazin (zeige CACNG2 Antikörper) has implications for information processing in the brain, because it should allow activity-dependent facilitation of excitatory synaptic transmission through a postsynaptic mechanism.
This study demonstrated that the GRIA4 protein was altered in auditory cortex patient with schizophreia.
Interaction with the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor subunit GluR4.
the levels were comparable for complexes containing GluR2 (zeige GRIA2 Antikörper), GluR3 (zeige GRIA3 Antikörper) and GluR4 as well as 5-HT1A (zeige HTR1A Antikörper). Moreover, the levels of complexes containing muscarinic AChR M1, NR1 (zeige GRIN1 Antikörper) and GluR1 (zeige GRIA1 Antikörper) were significantly increased in male patients with AD.
Statistical analysis showed no association between migraine and the GRIA2 (zeige GRIA2 Antikörper) and GRIA4 polymorphisms investigated.
The N-terminal domain modulates alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA (zeige GRIA3 Antikörper)) receptor desensitization.
The data potentially suggest a lack of epistatic interaction between GRIA2 (zeige GRIA2 Antikörper) and GRIA4 variants regarding clinical outcomes in patients with major depressive disorder.
Did not observed any significant association between GRIA4 polymorphisms and clinical improvement in patients with Major depressive disorder.
The central distribution of AMPARs is absent in GluA3 (zeige GRIA3 Antikörper)-knockout mice, and gold particles are evenly distributed along the postsynaptic density. GluA4 gold labeling was homogenously distributed along both synapse types. Thus, GluA3 (zeige GRIA3 Antikörper) and GluA4 subunits are distributed at auditory nerve synapses in a target-cell-dependent manner.
These data suggest that GluA4 enables efficient homeostatic upscaling and responsiveness to temporal activity patterns during the critical period of activity-dependent refinement of the circuitry.
this study shows that curcumin increased the GluR4 expression in bone marrow-derived dendritic cells activated with lipopolysaccharides, which likely contributed to the mechanism of inhibiting the Th17 cell differentiation
GluA4 subunits are required to produce an EPSC-triggerable postsynaptic action potentials after the presynaptic action potential, while Cav3.1 (zeige CACNA1G Antikörper) expression is needed to establish the driver function of L5B-POm synapses at hyperpolarized membrane potentials
Data indicate that the AMPA (zeige GRIA3 Antikörper) receptor subunits abundance is hippocampus, GluA2 (zeige GRIA2 Antikörper) > GluA1 (zeige GRIA1 Antikörper) > GluA3 (zeige GRIA3 Antikörper) >> GluA4; cortex, GluA2 (zeige GRIA2 Antikörper) > GluA3 (zeige GRIA3 Antikörper) >/= GluA1 (zeige GRIA1 Antikörper) >> GluA4; and cerebellum, GluA2 (zeige GRIA2 Antikörper) > GluA3 (zeige GRIA3 Antikörper) >/= GluA1 (zeige GRIA1 Antikörper) > GluA4.
Here we identify a novel modifier - called "pecanex-like 2", or Pcnxl2 (zeige PCNXL2 Antikörper) for short - that reduces the severity of spike-wave dischargesin the C3H substrain in which the Gria4 mutation originally arose
GluA4 expression is sufficient to alter the signaling mechanisms of synaptic plasticity and can fully explain the switch in the kinase dependency of long-term potentiation from PKA to Ca2+/calmodulin-dependent protein kinase II (zeige CAMK2G Antikörper) during synapse maturation.
Postsynaptic density fractions from spinal cord dorsal horns showed an increase in GluA4 expression after morphine discontinuation.
The GluA4 subunit of the AMPA (zeige GRIA3 Antikörper) receptor in the hippocampus (GluA4(HC-/-) mice) was ablated, thereby selectively reducing AMPA (zeige GRIA3 Antikörper) receptor-mediated currents onto a subgroup of hippocampal interneurons expressing GluA4.
study found the majority of cerebellar GluA1 (zeige GRIA1 Antikörper)/A4-type AMPARs are expressed in Bergmann glial (BG) cells; BG AMPARs are essential to optimize synaptic integration and cerebellar output function throughout life
Glutamate receptors are the predominant excitatory neurotransmitter receptors in the mammalian brain and are activated in a variety of normal neurophysiologic processes. These receptors are heteromeric protein complexes composed of multiple subunits, arranged to form ligand-gated ion channels. The classification of glutamate receptors is based on their activation by different pharmacologic agonists. The subunit encoded by this gene belongs to a family of AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate)-sensitive glutamate receptors, and is subject to RNA editing (AGA->GGA\; R->G). Alternative splicing of this gene results in transcript variants encoding different isoforms, which may vary in their signal transduction properties. Some haplotypes of this gene show a positive association with schizophrenia.
glutamate receptor, ionotrophic, AMPA 4
, AMPA receptor GluR4/D
, glutamate receptor subunit GluR4
, glutamate receptor 4
, AMPA-selective glutamate receptor 4
, glutamate receptor, ionotropic, AMPA4 (alpha 4)
, glutamate receptor channel alpha 4
, glutamate receptor ionotropic, AMPA 4
, spike wave 1