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Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. 再加上，我们可以发KCNJ2 蛋白 (5)和数多这个蛋白质的别的产品。
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Mammalian Monoclonal KCNJ2 Primary Antibody for ISt, IHC - ABIN1304735
DiFranco, Yu, Quiñonez, Vergara: Inward rectifier potassium currents in mammalian skeletal muscle fibres. in The Journal of physiology 2015
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Dog (Canine) Polyclonal KCNJ2 Primary Antibody for WB - ABIN2177159
Zhao, Xu, Yun, Zhao, Li, Gong, Yuan, Yan, Zhang, Ding, Wang, Zhang, Dong, Xiu, Yang, Liu, Xue, Li: Chronic obstructive sleep apnea causes atrial remodeling in canines: mechanisms and implications. in Basic research in cardiology 2014
Human Polyclonal KCNJ2 Primary Antibody for EIA, IHC (fro) - ABIN1107936
Hinard, Belin, Konig, Bader, Bernheim: Initiation of human myoblast differentiation via dephosphorylation of Kir2.1 K+ channels at tyrosine 242. in Development (Cambridge, England) 2008
We report a novel KCNJ2 sequence variant (p.Y145C) in a family with diagnosed Andersen-Tawil syndrome.
Combined inhibition of IKr and IKur produced a synergistic anti-arrhythmic effect in both forms of SQT3. In conclusion, this study provides mechanistic insights into atrial proarrhythmia with SQT3 Kir2.1 mutations and highlights possible pharmacological strategies for management of SQT3-linked AF.
Data suggest that an R204A mutation disrupts the characteristic cytoplasmic domain subunit interface salt bridges in Kir2.1 reducing apparent sensitivity of channel activity to ligand PIP2 (phosphatidylinositol bisphosphate).
These findings suggest that KCNJ2 plays an important role in the pathophysiology of Thyrotoxic Periodic Paralysis in Korean Graves' Disease patients with Thyrotoxic Periodic Paralysis .
Nav1.5 (显示 SCN5A 抗体) N-terminal domain binding to alpha1-syntrophin (显示 SNTA1 抗体) increases membrane density of human Kir2.1, Kir2.2 (显示 KCNJ12 抗体) and Nav1.5 (显示 SCN5A 抗体) channels
Kir2.1 may participate in macrophage maturation and differentiation, and play a key role in lipid uptake and foam cell formation through modulating the expression of scavenger receptors.
a Korean family with Andersen-Tawil syndrome with a G215D mutation of the KCNJ2 gene revealed by diagnostic exome sequencing, is reported.
Chloroethylclonidine interact with Kir2.1 channels in the cytoplasmic pore.
Variability has been found in a three-generation family with Pierre Robin sequence, acampomelic campomelic dysplasia, and intellectual disability due to a novel approximately 1 Mb deletion upstream of SOX9 (显示 SOX9 抗体), and including KCNJ2 and KCNJ16 (显示 KCNJ16 抗体).
Patients with Dilated Cardiomyopathy and Sustained Monomorphic Ventricular Tachycardia Show Up-Regulation of KCNN3 (显示 KCNN3 抗体) and KCNJ2 Genes and CACNG8 (显示 CACNG8 抗体)-Linked Left Ventricular Dysfunction
Following differentiation with LPS (显示 TLR4 抗体) or a combination of LPS (显示 TLR4 抗体) and IFN-gamma (显示 IFNG 抗体) microglia exhibited high KV 1.3 current densities ( approximately 50 pA/pF at 40 mV) and virtually no KCa (显示 CSN3 抗体) 3.1 and Kir (显示 GEM 抗体) currents, while microglia differentiated with IL-4 (显示 IL4 抗体) exhibited large Kir (显示 GEM 抗体) 2.1 currents ( approximately 10 pA/pF at -120 mV). KCa (显示 CSN3 抗体) 3.1 currents were generally low
Cellular electrophysiology assays of mouse Kir2.1 and human Kir2.2 indicated that, consistent with simulations, the Leu residue increased the channel responses to phosphatidylinositol diphosphate (PIP2) through increased binding affinity and faster activation kinetics, and the deactivation kinetics decreased upon PIP2 inhibition.
histone H4 (显示 HIST1H4H 抗体) hyperacetylation induced by Class I HDACs inhibitors promoted the expression profiles of potassium channels (Kcnj2, Kcnj3 (显示 KCNJ3 抗体), Kcnj5 (显示 KCNJ5 抗体), Kcnj11 (显示 KCNJ11 抗体), and Kcnh2 (显示 KCNH2 抗体))
Our results support the concept that endothelial cell Kir2 channels boost vasodilatory signals that are generated by Ca(2 (显示 CA2 抗体)+) -dependent activation of IK and SK channels.
Results suggest that a promyogenic cell adhesion molecule (显示 MCAM 抗体) Cdo (显示 CDO1 抗体) signaling is critical for Inward rectifier potassium channel Kir2.1 activities in the induction of myogenic differentiation.
The data suggest that microglial Kir2.1 channels may represent novel therapeutic targets to inhibit excessive reactive oxygen species production by primed microglia in brain pathology.
Three pairs of weak interactions precisely regulate the G-loop gate of Kir2.1 channel.
Suggest that Kir2.1 channels, in part, account for hyperpolarization and associated absence of tone in urinary bladder arterioles.
This finding represents the first functional evidence for a significant role of the dystrophin (显示 DMD 抗体)-associated protein complex in the regulation of Kir2.x channels.
Intracellular Mg(2 (显示 MCOLN1 抗体)+) and SPM (显示 NPC1 抗体) therefore may have a synergistic action on the pore-blocking effect, presumably via prohibition of the outward exit of the higher-affinity blocking SPM (显示 NPC1 抗体) by the lower-affinity Mg(2 (显示 MCOLN1 抗体)+).
Hypoxic stress up-regulates Kir2.1 expression and facilitates cell proliferation in brain capillary endothelial cells.
Kir2.1 may mediate native Kir (显示 GEM 抗体) currents responsible for setting resting membrane potential in bovine parotid cells and might be, at least in part, involved in spontaneous secretion in ruminant parotid glands.
There were substantial transmural gradients in Cav1.2 (显示 CACNA1C 抗体), KChIP2 (显示 KCNIP2 抗体), ERG (显示 KCNH2 抗体), KvLQT1 (显示 KCNQ1 抗体), Kir2.1, NCX1 (显示 SLC8A1 抗体), SERCA2a (显示 ATP2A2 抗体) and RyR2 (显示 RYR2 抗体) at the mRNA and, in some cases, protein level-in every case the mRNA or protein was more abundant in the epicardium than the endocardium.
Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, probably participates in establishing action potential waveform and excitability of neuronal and muscle tissues. Mutations in this gene have been associated with Andersen syndrome, which is characterized by periodic paralysis, cardiac arrhythmias, and dysmorphic features.
, inward rectifier K(+) channel Kir2.1
, inward rectifier potassium channel 2
, potassium channel, inwardly rectifying subfamily J member 2
, cardiac inward rectifier potassium channel
, inward rectifier K+ channel KIR2.1
, inward rectifier potassium channel cIRK1
, cardiac inward rectifier KIR2.1
, inwardly rectifying potassium channel Kir2.1
, inward rectifier potassium channel Kir2.1
, inwardly-rectifying potassium channel Kir2.1