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.
| Product Information | |
|---|---|
| Catalog #: | ACC-RI0072 | 
| Gene Name: | KCNJ2 | 
| Abbr | HEK293-HuCACNA1A/AP4B1/CACNA2D1/KCNJ2 | 
| Alias | KCNJ2,IRK1,Kir2.1,IRK-1,hIRK1,LQT7,SQT3,ATFB9,HHIRK1,KIR2.1,HHBIRK1 | 
| Channel Subgroup | Inwardly rectifying (Kir) | 
| Channel Type | Potassium Channel | 
| Growth Properties | Adherent | 
| Host Cell | HEK293 | 
| Morphology | Epithelial | 
| Product Format | frozen | 
| Product Type | Ion Channel Expressing Cell | 
| searchKeyword | KCNJ2,IRK1,Kir2.1,IRK-1,hIRK1,LQT7,SQT3,ATFB9,HHIRK1,KIR2.1,HHBIRK1 | 
| Shipping | Dry ice | 
| Species | Human | 
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