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GABRG2 encodes a gamma-aminobutyric acid (GABA) receptor. De plus, nous expédions GABRG2 Protéines (4) et beaucoup plus de produits pour cette protéine.
Showing 10 out of 117 products:
Human Polyclonal GABRG2 Primary Antibody pour IHC, WB - ABIN152532
Joshi, Sun, Kapur: A mouse monoclonal antibody against the γ2 subunit of GABAA receptors. dans Hybridoma (2005) 2011
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Human Polyclonal GABRG2 Primary Antibody pour ICC, IF - ABIN152497
Borghese, Werner, Topf, Baron, Henderson, Boehm, Blednov, Saad, Dai, Pearce, Harris, Homanics, Harrison: An isoflurane- and alcohol-insensitive mutant GABA(A) receptor alpha(1) subunit with near-normal apparent affinity for GABA: characterization in heterologous systems and production of knockin mice. dans The Journal of pharmacology and experimental therapeutics 2006
Show all 6 Pubmed References
Rat (Rattus) Polyclonal GABRG2 Primary Antibody pour WB - ABIN361439
Gomez, Froemke, Burden: Synaptic plasticity and cognitive function are disrupted in the absence of Lrp4. dans eLife 2014
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Human Monoclonal GABRG2 Primary Antibody pour ICC, IP - ABIN2690511
Kerti-Szigeti, Nusser: Similar GABAA receptor subunit composition in somatic and axon initial segment synapses of hippocampal pyramidal cells. dans eLife 2016
This study identified a missense de novo mutation in the GABAA (Montrer GABRg1 Anticorps) receptor gamma2 subunit, P302L, in a patient with Dravet syndrome. The mutation has a novel pathogenic mechanism to cause defects in the conductance and gating of GABAA (Montrer GABRg1 Anticorps) receptors, which results in hyperexcitability and contributes to the pathogenesis of the genetic epilepsy Dravet syndrome.
This study demonstrated that rescue of PTZ seizure threshold and thalamocortical oscillations in a Gabrg2+/Q390X KI mouse model of Dravet syndrome/GEFS+ by overexpression of wild-type gamma2HA subunits.
Defects in GABRG2/GABAergic neurotransmission participate in the pathogenesis of genetic epilepsies including epileptic encephalopathies.
This review suggest that the pathogenesis of GABRG2 mutations is likely to be due to a combination of reduction of channel function and disturbance of cellular homeostasis due to the presence of mutant protein.
Nova1 (Montrer NOVA1 Anticorps) interacts with GABAARgamma2 not only in the central nervous system but also in hepatocellular carcinoma. Nova1 (Montrer NOVA1 Anticorps)'s potential mechanism as an oncogene (Montrer RAB1A Anticorps) may due to its interaction with GABAA (Montrer GABRg1 Anticorps) Rgamma2.
Thus, the presence of active GABA-A receptors, associated with phenotype determination via Ca(2 (Montrer CA2 Anticorps)+)-signalling was demonstrated in differentiating human DA neurons.
common variants of GABRG2, RELN (Montrer RELN Anticorps) and NRG3 (Montrer NRG3 Anticorps) and the GABRG2-RELN (Montrer RELN Anticorps)-PTCH1 (Montrer PTCH1 Anticorps) interaction networks might confer altered susceptibility to Hirschsprung disease.
GABRG2, in combination with GABRA4 (Montrer GABRA4 Anticorps), is associated with autism spectrum disorder in an Argentine dataset.
Deletion of the N-terminal extension and putative alpha-helix in heteromeric alpha1beta2gamma2 GABAA (Montrer GABRg1 Anticorps) receptors in the gamma2 subunits reduced the number of functional receptors and incorporation into mature receptors.
Mutant GABRG2 may be responsible for genetic epilepsy as well neurodegeneration.
GABAA (Montrer GABRg1 Anticorps) receptor (GABAAR) and the Na(+)-K(+)-2Cl(-) cotransporter (Montrer SLC12A1 Anticorps) (NKCC1 (Montrer SLC12A2 Anticorps)), but not the K(+)-Cl(-) cotransporter (Montrer SLC12A4 Anticorps) (KCC2 (Montrer SLC12A5 Anticorps)), were expressed in the terminals of the CRH (Montrer CRH Anticorps) neurons at the median eminence (ME). In contrast, CRH (Montrer CRH Anticorps) neuronal somata were enriched with KCC2 (Montrer SLC12A5 Anticorps) but not with NKCC1 (Montrer SLC12A2 Anticorps).
This study demonstrated that the reduced local input to fast-spiking interneurons in the somatosensory cortex in the GABAA (Montrer GABRg1 Anticorps) gamma2 R43Q mouse model of absence epilepsy.
Heterozygous Gabrg2(+/Q390X) KI mice are associated with a severe epileptic encephalopathy due to a dominant negative effect of the mutation, while heterozygous Gabrg2(+/-) KO mice are associated with mild absence epilepsy due to simple haploinsufficiency.
This investigation demonstrates striking interfacial GABAA (Montrer GABRg1 Anticorps) receptor subunit selectivity in the native milieu, suggesting that asymmetric occupancy of heteropentameric ion channels by alkylphenol-based anesthetics is sufficient to induce modulation of activity.
Study shows that the down-regulation of the gamma2 subunit of postsynaptic GABAARs in NG2 (Montrer Vcan Anticorps) cells that accompanies the postnatal switch from synaptic to extrasynaptic GABAergic transmission between interneurons and these cells in the barrel cortex
Dendritic spine abnormalities of Gabrg2+/- mice suggest association of functional defects in glutamatergic transmission with the established anxious-depressive phenotype of these mice
KIF21B (Montrer KIF21B Anticorps) participates in the delivery of GABAAR transport vesicles into dendrites.
The study demonstrates the molecular and functional diversity of the GABAAR system within the mouse colon providing a framework for developing GABAAR-based therapeutics in GI disorders.
these findings suggest that gephyrin (Montrer GPHN Anticorps) may be a key factor in BDNF (Montrer BDNF Anticorps)-dependent GABAAR regulation in the amygdala.
This study showed that oscillatory activity in thalamic circuits is under the control of inhibition that involves gamma2 subunit-independent GABA-ARs (Montrer SLURP1 Anticorps)
This gene encodes a gamma-aminobutyric acid (GABA) receptor. GABA is the major inhibitory neurotransmitter in the mammlian brain, where it acts at GABA-A receptors, which are ligand-gated chloride channels. GABA-A receptors are pentameric, consisting of proteins from several subunit classes: alpha, beta, gamma, delta and rho. Mutations in this gene have been associated with epilepsy and febrile seizures. Multiple transcript variants encoding different isoforms have been identified for this gene.
gamma-aminobutyric acid A receptor, gamma 1
, GABA(A) receptor subunit gamma-2
, gamma-aminobutyric acid receptor subunit gamma-2
, gamma-aminobutyric acid A receptor gamma 2
, gamma-aminobutyric acid (GABA) A receptor, gamma 2
, gamma-aminobutyric acid receptor subunit gamma-2-like
, gamma-aminobutyric acid A receptor, gamma 2
, gamma-aminobutyric acid (GABA-A) receptor, subunit gamma 2
, gamma-aminobutyric acid A receptor, gamma 2
, GABA-A receptor gamma-2 subunit
, GABA(A) receptor, gamma 2