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KCNK9 encodes a member of the superfamily of potassium channel proteins containing two pore-forming P domains, and is highly expressed in the cerebellum. Additionally we are shipping KCNK9 Proteins (4) and many more products for this protein.
Showing 10 out of 26 products:
Mouse (Murine) Polyclonal KCNK9 Primary Antibody for IHC - ABIN350417
Czirjuak, Enyedi: TASK-3 dominates the background potassium conductance in rat adrenal glomerulosa cells. in Molecular endocrinology (Baltimore, Md.) 2002
Show all 3 references for ABIN350417
Mouse (Murine) Monoclonal KCNK9 Primary Antibody for ICC, IHC - ABIN2115251
Dadi, Luo, Vierra, Jacobson: TASK-1 Potassium Channels Limit Pancreatic ?-Cell Calcium Influx and Glucagon Secretion. in Molecular endocrinology (Baltimore, Md.) 2015
Show all 2 references for ABIN2115251
Chicken Polyclonal KCNK9 Primary Antibody for IHC, WB - ABIN2776216
Rusznák, Bakondi, Kosztka, Pocsai, Dienes, Fodor, Telek, Gönczi, Szucs, Csernoch: Mitochondrial expression of the two-pore domain TASK-3 channels in malignantly transformed and non-malignant human cells. in Virchows Archiv : an international journal of pathology 2008
TASK-1 (show KCNK3 Antibodies) and TASK-3 may form heterodimers in human atrial cardiomyocytes.
During conductance simulation experiments, both TASK-3 and TREK-1 (show KCNK2 Antibodies) channels were able to repolarise the membrane once AP threshold was reached
The findings of this study suggest that variations in KCNK9 genes are associated with both mild and severe persistent breast pain after breast cancer surgery.
Diacylglycerol mediates regulation of TASK1 and TASK3 potassium channels by GNAQ.
Interference with TASK-3 channel expression, therefore, induces caspase (show CASP3 Antibodies)-dependent and -independent apoptosis of melanoma cells, most likely via causing mitochondrial depolarization.
K2P3.1 (show KCNK3 Antibodies) and K2P9.1 undergo rapid dynamin (show DNM1 Antibodies)-dependent endocytosis
Mutations of KCNK9 or epigenetic disturbances within the PEG13 imprinted cluster do not significantly contribute to the cause of the developmental disabilities tested in this study.
Two SNPs replicated: the paternal rs2471083-C allele (located near the imprinted KCNK9 gene) and the paternal rs3091869-T allele (located near the SLC2A10 (show SLC2A10 Antibodies) gene) increased BMI equally (beta = 0.11 (SD), P<0.0027)
For KCNK9, two SNPs (i.e., rs3780039, rs11166921) were associated with the occurrence of preoperative breast pain.
We observed co-localization of the TASK-3 protein and a mitochondrial marker in the mitochondria of HaCaT cells.
results demonstrate that neurotensin (NT (show NTS Antibodies)) transiently increased the neuronal excitability of dentate gyrus granule cells (GCs (show UGCG Antibodies)) by inhibiting TASK-3 channels; NT-mediated increases in neuronal excitability facilitate long-term potentiation at the perforant path-GC synapses
KCNK9 channels are not involved in hearing.
THe results of this study suggested that dysfunction of KCNK9 causes a migration defect in the cortex via an activity-dependent mechanism.
Oxygen and mitochondrial inhibitors modulate both monomeric and heteromeric TASK-1 (show KCNK3 Antibodies) and TASK-3 channels in mouse carotid body type-1 cells.
Data indicate that in 1-day-old Task3-/- mice, renal renin (show REN Antibodies) concentration was lower than in wild-type mice.
DPP6 (show DPP6 Antibodies) co-expression with TASK-3 results in the formation of a protein complex that enhances resting membrane potassium conductance.
An extracellular ion pathway plays a central role in the cooperative gating of a K(2P) K+ channel (show KCNC4 Antibodies) by extracellular pH
Task3 plays an important role in the adaptation of aldosterone secretion to dietary salt intake.
This study demonistrated that kcnk9 gene expression in mouse dorsal raphe nucleus
TASK3 channel genes may contribute to the development of low renin (show REN Antibodies) essential hypertension and idiopathic hyperaldosteronism in mice.
This gene encodes a member of the superfamily of potassium channel proteins containing two pore-forming P domains, and is highly expressed in the cerebellum. Amplification and overexpression of this gene has been observed in several types of human carcinomas, notably in breast cancer. This gene is imprinted in fetal brain, with preferential expression from the maternal allele.
potassium channel, subfamily K, member 9
, TWIK-related acid-sensitive K(+) channel 3
, TWIK-related acid-sensitive K+ channel 3
, acid-sensitive potassium channel protein TASK-3
, potassium channel TASK3
, potassium channel subfamily K member 9
, two pore K(+) channel KT3.2
, two pore potassium channel KT3.2
, potassium channel subfamily K member 9 (Task-3)
, potassium channel, subfamily K, member 9 (Task-3)
, TASK-1 potassium channel