Kv7.1 (KCNQ1) is part of a voltage-gated K+ family that includes 5 other members (KCNQ1-5).
The channel has been intensively studied since it was found that together with MinK (Isk) it
underlay the cardiac Iks current that controls the duration of the action potential of the human heart.
Indeed mutations on either Kv7.1 or MinK can be responsible for long QT syndrome, a cardiac disorder
that causes arrhythmias and sudden death.
Although Kv7.1 expression and function has been mainly investigated in relation with cardiac function
the channel is widely distributed in epithelial tissues. There it has been implicated in physiological
functions such as: regulation of acid secretion in the stomach and Cl- secretion into the colon.
Alomone Labs is pleased to offer a highly specific antibody directed against an intracellular epitope of human Kv7.1. The Anti-Kv7.1 (KCNQ1) antibody (#APC-022) can be used for western blot analysis. It has been designed to recognize Kv7.1 from rat, human and mouse samples.