Anti-Human/Mouse/Rat KCNH2 Polyclonal Antibody

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.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA07849
Size 100μl
Host Type Rabbit
Immunogen Synthetic peptide of human KCNH2
Specificity Highly expressed in heart and brain.
Isotype IgG
Reacitivity Human,Mouse,Rat
Clone
Uniprot Q12809
Concentration 0.2 mg/mL
Dilution WB 1:500-1:2000
Formulation
Application WB,ELISA
Other Names eag homolog,Eag-related protein 1,ERG,ERG-1,ERG1,Ether a go go related potassium channel protein,Ether-a-go-go-related gene potassium channel 1,Ether-a-go-go-related protein 1,H ERG,H-ERG,HERG 1,HERG,hERG-1,hERG1,KCNH2,KCNH2,Kv11.1,LQT 2,LQT2,Potassium channel HERG,Potassium voltage gated channel subfamily H (eag related) member 2,Potassium voltage-gated channel subfamily H member 2,SQT1,Voltage gated potassium channel,subfamily H,member 2,Voltage-gated potassium channel subunit Kv11.1
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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