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anti-Human KCNE1 Antikörper:
anti-Rat (Rattus) KCNE1 Antikörper:
anti-Mouse (Murine) KCNE1 Antikörper:
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Human Polyclonal KCNE1 Primary Antibody für IF (p), IHC (p) - ABIN1385530
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 Monoclonal KCNE1 Primary Antibody für RNAi, ELISA - ABIN561579
Wang, Zankov, Jiang, Zhang, Henderson, Tseng: [Ca2+]i elevation and oxidative stress induce KCNQ1 protein translocation from the cytosol to the cell surface and increase slow delayed rectifier (IKs) in cardiac myocytes. in The Journal of biological chemistry 2013
TNIK (Traf2 and Nck-interacting kinase (zeige TNIK Antikörper)) and MINK (Misshapen/NIKs-related kinase) MAP4K signalling kinases are integral components of both canonical and non-canonical pathways in Xenopus.
KCNE1/KCNQ1 (zeige KCNQ1 Antikörper) was expressed in Xenopus oocytes with and without beta-catenin (zeige CTNNB1 Antikörper). Confocal microscopy revealed that beta-catenin (zeige CTNNB1 Antikörper) enhanced the KCNE1/KCNQ1 (zeige KCNQ1 Antikörper) protein abundance in the cell membrane.
PIP(2) has a role in KCNE1 modulation of I(Ks) channels that may represent a common mechanism of auxiliary subunit modulation of many ion channels
characterize a new component of the early bioelectrical circuit: the potassium channel (zeige KCNAB2 Antikörper) KCNQ1 (zeige KCNQ1 Antikörper) and its accessory subunit KCNE1
phenylboronic acid (PBA) activates KCNQ1 (zeige KCNQ1 Antikörper)/KCNE1 complexes
Equine KV7.1 (zeige KCNQ1 Antikörper)/KCNE1 expressed in CHO (zeige COL11A1 Antikörper)-K1 cells exhibited electrophysiological properties that are overall similar to the human orthologs; however, a slower deactivation was found which could result in more open channels at fast rates.
The KCNE1 (rs1805127) appears to an independent risk factor for AF in the Uygur population. And the KCNE4 (zeige KCNE4 Antikörper) (rs12621643) was an independent risk factor for AF among both Uygurs and Hans.
Western blotting analysis combined with these pharmacological data suggest that long-term insulin (zeige INS Antikörper) treatment augments KCNQ1 (zeige KCNQ1 Antikörper)/KCNE1 currents by increasing KCNE1 protein expression.
KCNQ1/KCNE1 channel does not require phosphatidylinositol-4,5-bisphosphate (PIP2) or phosphatidylinositol-4-phosphate for anterograde trafficking, but is heavily reliant on PIP2 for channel function once at the plasma membrane.
The genetic variant rs426496 in AQP2 (zeige AQP2 Antikörper); rs591810 in AQP3 (zeige AQP3 Antikörper) and rs1805127, rs1805128, and rs17173510, in KCNE1 were found in patients with Meniere's disease
Meta-analysis suggests that the G38S polymorphism in the KCNE1 gene can significantly increase the risk of atrial fibrillation in both Chinese and white individuals.
Sphingomyelin synthase 1 (zeige SGMS1 Antikörper) positively regulates KCNQ1 (zeige KCNQ1 Antikörper)/KCNE1 channel density in a protein kinase D (zeige PRKD1 Antikörper)-dependent manner.
Receptor Species-dependent Desensitization Controls KCNQ1 (zeige KCNQ1 Antikörper)/KCNE1 K+ Channels as Downstream Effectors of Gq Protein-coupled Receptors.(
KCNE1 encodes a modulator of KCNQ1 (zeige KCNQ1 Antikörper) and KCNH2 (zeige KCNH2 Antikörper) channels. Long QT syndrome (LQTS) patients with KCNE1(G38S) had a rate-dependent repolarization abnormality similar to patients with LQT2 (zeige KCNH2 Antikörper) and, therefore, may have a potential risk to develop lethal arrhythmias.
A stoichiometry of 4:4 between the alpha KCNE1 and the beta KCNQ1 (zeige KCNQ1 Antikörper)-subunits has been established.
miR-1 by anti-miR-1 inhibitor oligonucleotides alleviated the downregulation of KCNE1 and KCNB2 (zeige KCNB2 Antikörper), the shortening of AERP, and the increase in the IKs
The localization of KCNE1 in the RPE (zeige RPE Antikörper) basal membrane, where KCNQ5 (zeige KCNQ5 Antikörper) was previously found to be present, suggests that this beta-subunit (zeige POLG Antikörper) may contribute to M-type K(+) channels in this membrane.
The electrophysiological effects of BACE1 (zeige BACE Antikörper) on KCNQ1 (zeige KCNQ1 Antikörper) reported here were independent of its enzymatic activity.
KCNE1 and KCNE3 (zeige Kcne3 Antikörper): The yin and yang of voltage-gated K(+) channel (zeige KCND3 Antikörper) regulation
KCNE1 and KCNE2 (zeige KCNE2 Antikörper), auxiliary subunits of voltage-gated potassium channels, undergo sequential cleavage mediated by either alpha-secretase and presenilin(PS)/gamma-secretase or BACE1 (zeige BACE Antikörper) and PS/gamma-secretase in cells.
In clearance studies the KCNE1 knockout mice had an increased fractional excretion of Na+, Cl-, HCO3(-) and water.
This study confirmed that KCNE1 channels are necessary for K+ secretion in developmental Saccule and Utricle in mice.
both the voltage-dependence and kinetics of gating were found to depend on the relative densities of KCNQ1 (zeige KCNQ1 Antikörper) and KCNE1, suggesting the heart rhythm may be regulated by the relative expression of the auxiliary subunit
Findings directly implicate triggered electrical activity and spatial and temporal re-entrant mechanisms in the arrhythmogenesis observed in KCNE1 (-/-) hearts.
intestinal Cl(-) secretion is independent from KCNE1 but requires KCNQ1 (zeige KCNQ1 Antikörper) and in mouse pancreatic acini KCNQ1 (zeige KCNQ1 Antikörper) probably co-assembled with KCNE1 leads to a voltage-dependent K(+) current that might be of importance for electrolyte and enzyme secretion.
the spatial expression of minK-lacZ (zeige GLB1 Antikörper) in the adult mouse heart has been shown, for the larger part, to be coincident with the conduction tissues
The transitory transfection of kcne1 restores both Cl- and K+ swelling-activated currents, confirming the implication of KCNE1 protein in the cell-volume regulation in PCT (zeige UROD Antikörper) cells in primary cultures.
The product of this gene belongs to the potassium channel KCNE family. Potassium ion channels are essential to many cellular functions and show a high degree of diversity, varying in their electrophysiologic and pharmacologic properties. This gene encodes a transmembrane protein known to associate with the product of the KVLQT1 gene to form the delayed rectifier potassium channel. Mutation in this gene are associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long-QT syndrome. Alternatively spliced transcript variants encoding the same protein have been identified.
potassium voltage-gated channel, Isk-related family, member 1
, voltage-gated potassium channel subunit MinK
, potassium voltage-gated channel subfamily E member 1
, IKs producing slow voltage-gated potassium channel subunit beta Mink
, cardiac delayed rectifier potassium channel protein
, delayed rectifier potassium channel subunit IsK
, minimal potassium channel
, potassium voltage-gated channel, Isk-related subfamily, member 1
, voltage gated potassiun channel accessory subunit
, potassium (K+) channel protein, slowly activating (Isk)
, potassium voltage-gated channel Shaw-related subfamily member 1
, delayed rectifier potassium channel protein
, slow delayed rectifier K+ channel
, voltage gated potassium channel accessory subunit cardiac splice