KCNJ10 多克隆抗体

免疫组织化学（IHC）已验证样本:Human esophagus cancer

IHC 1:50-1:200, ELISA 1:5000-1:10000

Polyclonal

IgG

Fusion protein of human KCNJ10

KCNJ10

inwardly rectifying subfamily J member 10;ATP dependent inwardly rectifying potassium channel Kir4.1;ATP sensitive inward rectifier potassium channel 10;ATP-dependent inwardly rectifying potassium channel Kir4.1;ATP-sensitive inward rectifier potassium channel 10;BIRK10;Glial ATP dependent inwardly rectifying potassium channel KIR4.1;Inward rectifier K(+) channel Kir1.2;Inward rectifier K+ channel KIR1.2;Inwardly rectifying potassium channel Kir1.2;KCJ10;KCNJ 10;Kcnj10;KCNJ13 PEN;KIR1.2;KIR4.1;Potassium channel;Potassium channel inwardly rectifying subfamily J member 10;Potassium inwardly rectifying channel subfamily J member 10;SESAME抗体

P78508

Membrane. Basolateral cell membrane. In kidney distal convoluted tubules, located in the basolateral membrane where it colocalizes with KCNJ16.

1.08 mg/mL

在-20℃下储存有效期为12个月。 避免冻融循环。

PBS with 0.05% NaN3 and 40% Glycerol,pH7.4

Antigen affinity purification

Neuroscience

Unconjugated

KCNJ10 (Potassium Voltage-Gated Channel Subfamily J Member 10) is a Protein Coding gene. Diseases associated with KCNJ10 include Sesame Syndrome and Deafness, Autosomal Recessive 4, With Enlarged Vestibular Aqueduct. Among its related pathways are Inwardly rectifying K+ channels and GABA receptor activation. GO annotations related to this gene include identical protein binding and potassium channel activity. An important paralog of this gene is KCNJ15.This gene encodes a member of the inward rectifier-type potassium channel family, characterized by having a greater tendency to allow potassium to flow into, rather than out of, a cell. The encoded protein may form a heterodimer with another potassium channel protein and may be responsible for the potassium 缓冲ing action of glial cells in the brain. Mutations in this gene have been associated with seizure susceptibility of common idiopathic generalized epilepsy syndromes.