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KCNK2 encodes one of the members of the two-pore-domain background potassium channel protein family. Additionally we are shipping KCNK2 Proteins (4) and many more products for this protein.
Showing 10 out of 46 products:
Cow (Bovine) Polyclonal KCNK2 Primary Antibody for WB - ABIN188929
Zhang, Yin, Wang, Li, Wang: Over-expressed human TREK-1 inhibits CHO cell proliferation via inhibiting PKA and p38 MAPK pathways and subsequently inducing G1 arrest. in Acta pharmacologica Sinica 2016
ANG II inhibits bTREK-1 K(+) channels by a Ca(2+)-dependent mechanism that does not require the depletion of membrane-associated PIP(2).
Metabolites of cAMP stimulate TREK-1 expression in adrenal cortex cells by activation of a novel cAMP-independent mechanism.
TREK-1 channels may function as sensors that couple the metabolic state of the cell to membrane potential, perhaps through an associated ATP-binding protein
These results identify bTREK-1 K(+) channels as a pivotal control point where ANG II (show AGT Antibodies) receptor activation is transduced to depolarization-dependent Ca(2 (show CA2 Antibodies)+) entry and aldosterone secretion.
Data show that angiotensin II and paracrine factors that act through phospholipase C (show PLC Antibodies) inhibit bTREK-1 in adrenocortical cells through simultaneous activation of separate Ca2 (show CA2 Antibodies)+- and ATP hydrolysis-dependent signaling pathways.
Angiotensin II (ANGII) inhibits adrenocortical cell KCNK2 in an ATP dependent, PLC/PKC independent manner.
These findings demonstrate that, in addition to the well-described PKA-dependent TREK-1 inhibition, ACTH (show POMC Antibodies), NPS (show NPS Antibodies)-ACTH (show POMC Antibodies), forskolin, and 8-pCPT-2'-O-Me-cAMP also inhibit these K(+) channels by a PKA-independent signaling pathway.
Atrial TREK-1 expression was reduced in atrial fibrillation patients with concomitant severe heart failure
The authors identified a heterozygous point mutation in the selectivity filter of the stretch-activated K2P potassium channel (show KCNAB2 Antibodies) TREK-1 (KCNK2 or K2P2.1). This mutation introduces abnormal sodium permeability and stretch-activation hypersensitivity to TREK-1.
The M2-glycine hinge controls the macroscopic currents of TREK1 channels.
TREK-1 overexpression suppresses CHO (show COL11A1 Antibodies) cell proliferation by inhibiting the activity of PKA and p38/MAPK (show MAPK14 Antibodies) signaling pathways and subsequently inducing G1 phase cell arrest.
Trek1 expression facilitates the restoration of intestinal epithelial barrier functions in an allergic environment.
presence of TREK-1 variants correlated to reduced TREK-1 activity, suggesting a pathological role for TREK-1 variants in preterm labor
Data suggest that potassium channel protein (show KCNQ5 Antibodies) TREK-1 (TREK-1) might be a biomarker in castration resistance free survival (CRFS) judgment of prostate cancer (PCa (show FLVCR1 Antibodies)), as well as a potential therapeutic target.
During conductance simulation experiments, both TASK-3 (show KCNK9 Antibodies) and TREK-1 channels were able to repolarise the membrane once AP threshold was reached
How ion channels sense mechanical force: insights from mechanosensitive K2P channels TRAAK (show KCNK4 Antibodies), TREK1, and TREK2 (show KCNK10 Antibodies).
We conclude that Trek1 is critical to maintain the nasal epithelial barrier function.
TREK-1 deficiency promoted neurons and oligodendrocytes apoptosis, aggravated demyelination and retarded motor recovery following spinal cord injury.
Formation of TREK-1/TREK-2 (show KCNK10 Antibodies) channels was also demonstrated in native dorsal root ganglion neurons indicating that heterodimerization may provide greater diversity of leak K(+) conductances also in native tissues.
Data suggest that porosome-associated proteins SNAP25 (show SNAP25 Antibodies), TREK-1, syntaxin-1A (show STX1A Antibodies), and Gai3 exhibit stability and functionality such that isolated proteins can be reconstituted as insulin (show INS Antibodies)-secreting porosomes in cell membrane of live cells.
Data indicate that arginine vasopressin (AVP (show AVP Antibodies)) and corticotropin-releasing hormone (CRH (show CRH Antibodies)) show additive effects on the suppression of the potassium channel subfamily K member 2 TREK-1 current via protein kinase C (show PKC Antibodies).
TWIK-1 (show KCNK1 Antibodies)/TREK-1 heterodimers mediate astrocytic passive conductance and cannabinoid-induced glutamate (show GRIN1 Antibodies) release from astrocytes.
In TREK1-deficient mice, brain endothelial cells displayed an inflammatory phenotype.
provide new insight into membrane targeting of TREK-1 in the heart and establish a broader role for beta(IV)-spectrin (show SPTBN4 Antibodies) in organizing functional membrane domains critical for normal heart function
TREK-1 channels significantly contribute to the responsiveness of Grueneberg ganglion neurons to cool temperatures.
direct activation of the TREK-1 K(+) channel, acting downstream from the mu opioid receptor (show OPRM1 Antibodies), might have strong analgesic effects without opioid-like adverse effects
This gene encodes one of the members of the two-pore-domain background potassium channel protein family. This type of potassium channel is formed by two homodimers that create a channel that leaks potassium out of the cell to control resting membrane potential. The channel can be opened, however, by certain anesthetics, membrane stretching, intracellular acidosis, and heat. Three transcript variants encoding different isoforms have been found for this gene.
potassium channel subfamily K member 2
, potassium channel, subfamily K, member 2
, potassium channel subfamily K member 2-like
, K2P2.1 potassium channel
, TREK-1 K(+) channel subunit
, TWIK-related potassium channel 1
, outward rectifying potassium channel protein TREK-1
, potassium inwardly-rectifying channel, subfamily K, member 2
, tandem-pore-domain potassium channel TREK-1
, two pore domain potassium channel TREK-1
, two pore potassium channel TPKC1
, two-pore potassium channel 1
, arachidonic acid sensitive tandem pore domain potassium channel
, ion transport membrane protein