Transfected cell immunofluorescence: COS-1 cells expressing KCNQ1. Red = N37A/10, Blue = Hoechst nuclear stain.
Anti-Kv7.1/KCNQ1 K+ Channel Antibody
Kv7.1/KCNQ1 K+ channel
Potassium voltage-gated channel subfamily Q member 1 is encoded by the gene KCNQ1. KCNQ1 is a member of the potassium channel family, KQT (TC 1.A.1.15) subfamily, Kv7.1/KCNQ1 sub-subfamily. KCNQ1 is a voltage-gated potassium channel that is required for the repolarization phase of the cardiac action potential. KCNQ1 can form heteromultimers with two other potassium channel proteins, KCNE1 and KCNE3. KCNQ1 is expressed in the heart, pancreas, kidney, prostate, small intestine, and peripheral blood leukocytes. Diseases associated with KCNQ1 include Long QT Syndrome1, Jervell and Lange-Nielsen Syndrome, atrial fibrillation familial 3, short QT syndrome 2, and atrial fibrillation.
IHC, IP, WB
KCNQ1 KCNA8 KCNA9 KVLQT1
Fusion protein amino acids 2-101 of human KCNQ1(Kv7.1, KvLQT1, accession number P51787); Rat: 72% identity (71/98 amino acids identical); Mouse: 63% identity (62/98 amino acids identical)
Human, Mouse, Rat
Store at ≤ -20 C for long term storage. For short term storage, store at 2-8 C. For maximum recovery of product, centrifuge the vial prior to removing the cap.
No cross-reactivity reported
These antibodies are to be used as research laboratory reagents and are not for use as diagnostic or therapeutic reagents in humans.