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KCNJ12 encodes an inwardly rectifying K+ channel which may be blocked by divalent cations. Additionally we are shipping Potassium Inwardly-Rectifying Channel, Subfamily J, Member 12 Proteins (5) and many more products for this protein.
Showing 10 out of 85 products:
Human Monoclonal KCNJ12 Primary Antibody for ICC, IF - ABIN361770
Zobel, Cho, Nguyen, Pekhletski, Diaz, Wilson, Backx: Molecular dissection of the inward rectifier potassium current (IK1) in rabbit cardiomyocytes: evidence for heteromeric co-assembly of Kir2.1 and Kir2.2. in The Journal of physiology 2003
Show all 2 references for ABIN361770
Human Monoclonal KCNJ12 Primary Antibody for ICC, IF - ABIN2483477
Donaldson, Yoon, Fu, Ptacek: Andersen-Tawil syndrome: a model of clinical variability, pleiotropy, and genetic heterogeneity. in Annals of medicine 2004
Cow (Bovine) Polyclonal KCNJ12 Primary Antibody for WB - ABIN2776235
Ji, Foo, ORoak, Zhao, Larson, Simon, Newton-Cheh, State, Levy, Lifton: Rare independent mutations in renal salt handling genes contribute to blood pressure variation. in Nature genetics 2008
Nav1.5 (show SCN5A Antibodies) N-terminal domain binding to alpha1-syntrophin (show SNTA1 Antibodies) increases membrane density of human Kir2.1 (show KCNJ2 Antibodies), Kir2.2 and Nav1.5 (show SCN5A Antibodies) channels
The augmentation of Ca(2 (show CA2 Antibodies)+) influx and cytokine release suggests a physiological role for Kir2.2 in TLR4 (show TLR4 Antibodies)-stimulated monocytes.
Unconventional role of the inwardly rectifying potassium channel (show KCNAB2 Antibodies) Kir2.2 as a constitutive activator of RelA (show NFkBP65 Antibodies) in cancer.
Kir2.1 (show KCNJ2 Antibodies) and Kir2.2 have two distinct lipid requirements for activity.
Kir2.2 knockdown induces senescence of cancer cells by a mechanism involving reactive oxygen species accumulation.
Kir2.1 (show KCNJ2 Antibodies) and Kir2.2 subunits exert neither a dominant nor an anomalous effect on any of the properties of heteromeric channels.
KIr2.1 (show KCNJ2 Antibodies) and Kir2.2 are directly activated by membrane phosphatidylinositol 4,5-bisphosphate.
Molecular cloning of functional KCNJ12 with an arginine residue at position 285.
transcripts for Kir2.2 potassium channels are identified in proliferative smooth muscle cells
Kir2.2 and Kir2.1 (show KCNJ2 Antibodies) are primary determinants of endogenous K(+) conductance in HAECs under resting conditions and that Kir2.2 provides the dominant conductance in these cells.
Kir2.2 in the brainstem plays a transient role in hypercapnic ventilatory response , possibly through central ventilatory chemosensitivity, during postnatal development.
Computer simulations grounded in biophysical measurements of prelimbic and infralimbic cortex slices suggest a dynamic interaction among Kir2, Kleak, and HCN channel currents in shaping membrane potential and temporal integration of synaptic potentials.
This gene encodes an inwardly rectifying K+ channel which may be blocked by divalent cations. This protein is thought to be one of multiple inwardly rectifying channels which contribute to the cardiac inward rectifier current (IK1). The gene is located within the Smith-Magenis syndrome region on chromosome 17.
ATP-sensitive inward rectifier potassium channel 12
, inward rectifier K(+) channel Kir2.2
, potassium channel, inwardly rectifying subfamily J member 12
, potassium inwardly-rectifying channel, subfamily J, member 12
, inwardly-rectifying potassium channel Kir2.2
, inward rectifier K(+) channel Kir2.2v
, inward rectifier K(+) channel Kir2.6
, potassium inwardly-rectifying channel, subfamily J, inhibitor 1
, atrium potassium channel IRK
, potassium inwardly-rectifying channel J12