| Background: | This gene encodes a voltage-activated potassium channel belonging to the eag family. It shares sequence similarity with the Drosophila ether-a-go-go (eag) gene. Mutations in this gene can cause long QT syndrome type 2 (LQT2). Transcript variants encoding distinct isoforms have been identified. Pore-forming (alpha) subunit of voltage-gated inwardly rectifying potassium channel. Channel properties are modulated by cAMP and subunit assembly. Mediates the rapidly activating component of the delayed rectifying potassium current in heart (IKr). Isoform 3 has no channel activity by itself, but modulates channel characteristics when associated with isoform 1. | 
| Applications: | ELISA, WB | 
| Name of antibody: | KCNH2 | 
| Immunogen: | Synthetic peptide of human KCNH2 | 
| Full name: | potassium voltage-gated channel, subfamily H (eag-related), member 2 | 
| Synonyms: | ERG1, HERG, LQT2, SQT1, HERG1, Kv11.1 | 
| SwissProt: | Q12809 | 
| ELISA Recommended dilution: | 1000-5000 | 
| WB Predicted band size: | 90 kDa | 
| WB Positive control: | Mouse brain tissue | 
| WB Recommended dilution: | 500-2000 | 
 
 
	
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