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Human CACNA1A/AP4B1/CACNA2D1/KCNJ2 Stable Cell Line-HEK293

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Cat.No.
CSC-RI0072
Background
The human CACNA1A gene encodes the pore-forming subunit of Cav2.1, the voltage-gated P/Q-type calcium channel. Inclusion of auxiliary subunits modulate gating and pharmacological characteristics, while the inwardly rectifying potassium channel allows the membrane potential to be altered with changes in extracellular K+. Mutations in CACNA1A are responsible for several inherited neurologic disorders including, familial hemiplegic migraine, episodic ataxia type2, and spinocerebellar ataxia type 6 epilepsy. Cav2.1 channels expressed in neurons are therapeutic targets in pain.
Growth Properties
Adherent
Morphology
Epithelial
Host Cell
HEK293
Ship
Dry ice
Gene Information
Official Symbol
KCNJ2
Synonyms
KCNJ2; potassium inwardly-rectifying channel, subfamily J, member 2; inward rectifier potassium channel 2; IRK1; Kir2.1; IRK-1; hIRK1; inward rectifier K+ channel KIR2.1; cardiac inward rectifier potassium channel; LQT7; SQT3; ATFB9; HHIRK1; KIR2.1; HHBIRK1;
Gene ID
MIM
UniProt ID
P63252
Chromosome Location
17q24.3
Pathway
Activation of G protein gated Potassium channels, organism-specific biosystem; Activation of GABAB receptors, organism-specific biosystem; Cholinergic synapse, organism-specific biosystem; Classical Kir channels, organism-specific biosystem; G protein gated Potassium channels, organism-specific biosystem; GABA B receptor activation, organism-specific biosystem; GABA receptor activation, organism-specific biosystem;
Function
inward rectifier potassium channel activity; voltage-gated ion channel activity;

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