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The ASIC2 are involved in fear behaviours, learning and memory functions, and pain sensation.
The results show that acid-sensing ion channel 1 (zeige ACCN2 ELISA Kits), acid-sensing ion channel 2, and acid-sensing ion channel 3 (zeige ACCN3 ELISA Kits) are expressed in A549 cells at the messenger RNA and protein levels, and acid-sensing ion channel (zeige ACCN2 ELISA Kits)-like currents were elicited by extracellular acid stimuli.
results demonstrate the occurrence of ASIC2 and TrkB (zeige NTRK2 ELISA Kits) in the human intervertebral disc (IVD (zeige IVD ELISA Kits)), and the increased expression of both in pathological IVD (zeige IVD ELISA Kits) suggest their involvement in IVD (zeige IVD ELISA Kits) degeneration
distribution of ASIC2 in the human cutaneous mechanosensory system and suggest the involvement of ASIC2 in mechanosensation
This study suggests that ASIC2 may play a role as mediators of inflammatory pain and be involved in the pathogenesis of frozen shoulder.
Combinatorial analysis suggests a model of random mixing of ASIC1a (zeige ACCN2 ELISA Kits) and ASIC2a subunits to yield both 2:1 and 1:2 ASIC1a:ASIC2a heteromers together with ASIC1a (zeige ACCN2 ELISA Kits) and ASIC2a homomers.
The results showed that there was a significant increase in the mean relative optical density of ASIC2 and ASIC3 (zeige ACCN3 ELISA Kits) but not ASIC1a (zeige ACCN2 ELISA Kits) in the lining epithelium and glandular tubes of gastric mucosa in patients with Henoch-Schonlein purpura.
ACCN1 might be one of numerous susceptibility genes for panic disorder.
these results indicate that ACCN1 gene is a potential candidate for response to lithium treatment that would serve as a genetic marker of lithium efficacy for bipolar disorder patients.
These results demonstrate for the first time the differential distribution of ASIC1 (zeige ACCN2 ELISA Kits) and ASIC2 in human rapidly adapting low-threshold mechanoreceptors, and suggest specific roles of both proteins in mechanotransduction.
the potentiation of ASICs by quinine depends on the presence of the ASIC1a (zeige ACCN2 ELISA Kits), ASIC2a subunits, but not ASIC1b, ASIC3 (zeige ACCN3 ELISA Kits) subunits. Furthermore, we have determined the amino acids in ASIC1a (zeige ACCN2 ELISA Kits) that are involved in the modulation of ASICs by pHi.
ASIC2 deletion significantly protected the mouse brain from ischemic damage in vivo.
Studies with ASIC1a (zeige ACCN2 ELISA Kits)-ASIC2a chimeras showed that swapping the thumb domain between subunits results in faster channel desensitization. Likewise, the covalent modification of Cys (zeige DNAJC5 ELISA Kits) residues at selected positions in the beta-ball-thumb interface accelerates the desensitization of the mutant channels.
differential surface trafficking of ASIC1a (zeige ACCN2 ELISA Kits), ASIC2a, and ASIC2b, was investigated.
These data identify the LL motifs as a negative regulator of ASIC2a trafficking and function, and suggest novel regulatory mechanisms in acid signaling.
ASIC2 contributes to transduction of the renal myogenic response and has a protective role against renal injury and hypertension.
These results lend support to an emerging role of ASIC2 in the targeting of ASICs to surface membranes, and allows for interaction with PSD-95 (zeige DLG4 ELISA Kits) to regulate these processes.
A previously unknown postsynaptic current during neurotransmission mediated by ASIC1A (zeige ACCN2 ELISA Kits) and ASIC2 is well positioned to regulate synapse structure and function.
ASIC2 knockout mice showed less sensitization to challenge cocaine when compared to wild-type.
Currents from ASIC1a (zeige ACCN2 ELISA Kits)(-/-) muscle afferents were less pH-sensitive and displayed faster recovery, currents from ASIC2(-/-) showed diminished potentiation by zinc, and currents from ASIC3 (zeige ACCN3 ELISA Kits)(-/-) displayed slower desensitization than those from wild-type.
These results are the first demonstration that ASIC2 and ASIC4 (zeige ACCN4 ELISA Kits) are expressed in the adult zebrafish retina
The ASIC2 expression in this location might be related to detection of aquatic environment pH variations or to detection of water movement through the nasal cavity.
Muscles from horses submitted to strenuous exercises produce lactic acid, which may induce variable pain through ACCN differential properties; ACCN1 (zeige ACCN2 ELISA Kits) and ACCN3 (zeige ACCN3 ELISA Kits) genes have an ubiquitous expression but ACCN1 (zeige ACCN2 ELISA Kits) is more highly expressed in the spinal cord.
This gene encodes a member of the degenerin/epithelial sodium channel (DEG/ENaC) superfamily. The members of this family are amiloride-sensitive sodium channels that contain intracellular N and C termini, 2 hydrophobic transmembrane regions, and a large extracellular loop, which has many cysteine residues with conserved spacing. The member encoded by this gene may play a role in neurotransmission. In addition, a heteromeric association between this member and acid-sensing (proton-gated) ion channel 3 has been observed to co-assemble into proton-gated channels sensitive to gadolinium. Alternative splicing has been observed at this locus and two variants, encoding distinct isoforms, have been identified.
acid-sensing ion channel 2
, amiloride-sensitive cation channel 1, neuronal
, brain sodium channel 1
, mammalian degenerin homolog
, neuronal amiloride-sensitive cation channel 1
, amiloride-sensitive brain sodium channel
, amiloride-sensitive cation channel 1, neuronal (degenerin)
, amiloride-sensitive brain sodium channel 2
, acid-sensing (proton-gated) ion channel 2