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The product of KCNE1 belongs to the potassium channel KCNE family. Additionally we are shipping KCNE1 Proteins (8) and KCNE1 Kits (3) and many more products for this protein.
Showing 10 out of 63 products:
Human Monoclonal KCNE1 Primary Antibody for ELISA - ABIN395293
Bailey, Xie, Do, Montpetit, Diaz, Mohan, Keavney, Yusuf, Gerstein, Engert, Anand: Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study. in Diabetes Care 2010
Show all 5 references for ABIN395293
Human Monoclonal KCNE1 Primary Antibody for WB - ABIN396530
Siem, Fagerheim, Jonsrud, Laurent, Teig, Harris, Leren, Früh, Heimdal: Causes of hearing impairment in the Norwegian paediatric cochlear implant program. in International journal of audiology 2010
Show all 5 references for ABIN396530
Human Monoclonal KCNE1 Primary Antibody for 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
Human Polyclonal KCNE1 Primary Antibody for 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
TNIK (Traf2 and Nck-interacting kinase (show TNIK Antibodies)) and MINK (Misshapen/NIKs-related kinase) MAP4K signalling kinases are integral components of both canonical and non-canonical pathways in Xenopus.
KCNE1/KCNQ1 (show KCNQ1 Antibodies) was expressed in Xenopus oocytes with and without beta-catenin (show CTNNB1 Antibodies). Confocal microscopy revealed that beta-catenin (show CTNNB1 Antibodies) enhanced the KCNE1/KCNQ1 (show KCNQ1 Antibodies) 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 (show KCNAB2 Antibodies) KCNQ1 (show KCNQ1 Antibodies) and its accessory subunit KCNE1
phenylboronic acid (PBA) activates KCNQ1 (show KCNQ1 Antibodies)/KCNE1 complexes
Analysis of QT-RR relationship could also evaluate the latent arrhythmogenicity of KCNE1(G38S).
The incidence of AF among the senior Uygur population in Xinjiang territory was correlated with the KCNE1 (G38S) polymorphism, which may be an independent risk factor for Uygur AF patients.
The KCNQ1 (show KCNQ1 Antibodies) F279I mutation induces a gain of function of IKs due to an impaired gating modulation of Kv7.1 (show KCNQ1 Antibodies) induced by KCNE1, leading to a shortening of the cardiac action potential
This study aimed to assess the associations between polymorphisms on KCNE1, KCNQ1 (show KCNQ1 Antibodies), and KCNH2 (show KCNH2 Antibodies) with the risk of AF in a Chinese population.
KCNE1 and KCNE3 (show Kcne3 Antibodies): The yin and yang of voltage-gated K(+) channel (show KCND3 Antibodies) regulation
Two phenylalanine residues on KCNQ1 (show KCNQ1 Antibodies), Phe232 on S4 (VSD) and Phe279 on S5 (pore domain) to be responsible for the gating modulation by KCNE1.
acute application of PUFAs increases Kv7.1 (show KCNQ1 Antibodies)/KCNE1 through a probably direct effect, and shows antiarrhythmic efficacy under IKr block.
IKs phosphorylation and alpha1-AR regulation via activation of calcium-dependent PKC isoforms (cPKC) may be a key mechanism to control channel voltage-dependent activation and consequently action potential duration (APD) in response to adrenergic-stimulus.
KCNE1 distal C-terminus appears essential for the regulation of yotiao (show AKAP9 Antibodies)-mediated PKA phosphorylation.
the KCNE1 112G polymorphism may be a risk factor for AF. KCNE1 112G>A may be useful as a biomarker for predicting the development of AF.
study demonstrated that in the left ventricle,the level of the transcriptional product of KCNE1 was significantly higher than those of KCNQ1 (show KCNQ1 Antibodies), KCNH2 (show KCNH2 Antibodies), and KCNE2 (show KCNE2 Antibodies)
miR-1 by anti-miR-1 inhibitor oligonucleotides alleviated the downregulation of KCNE1 and KCNB2 (show KCNB2 Antibodies), the shortening of AERP, and the increase in the IKs
The localization of KCNE1 in the RPE (show RPE Antibodies) basal membrane, where KCNQ5 (show KCNQ5 Antibodies) was previously found to be present, suggests that this beta-subunit (show POLG Antibodies) may contribute to M-type K(+) channels in this membrane.
The electrophysiological effects of BACE1 (show BACE Antibodies) on KCNQ1 (show KCNQ1 Antibodies) reported here were independent of its enzymatic activity.
KCNE1 and KCNE2 (show KCNE2 Antibodies), auxiliary subunits of voltage-gated potassium channels, undergo sequential cleavage mediated by either alpha-secretase and presenilin(PS)/gamma-secretase or BACE1 (show BACE Antibodies) 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 (show KCNQ1 Antibodies) 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 (show KCNQ1 Antibodies) and in mouse pancreatic acini KCNQ1 (show KCNQ1 Antibodies) 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 (show GLB1 Antibodies) 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 (show UROD Antibodies) 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