Rabbit
WB,ELISA
Human
WB 1:500-2000 ELISA 1:5000-20000
-20°C/1 year
KCNQ1 Polyclonal Antibody detects endogenous levels of protein.
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Synthesized peptide derived from human protein . at AA range: 350-430
P51787
Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
Polyclonal
IgG
potassium voltage-gated channel subfamily Q member 1(KCNQ1) Homo sapiens This gene encodes a voltage-gated potassium channel required for repolarization phase of the cardiac action potential. This protein can form heteromultimers with two other potassium channel proteins, KCNE1 and KCNE3. Mutations in this gene are associated with hereditary long QT syndrome 1 (also known as Romano-Ward syndrome), Jervell and Lange-Nielsen syndrome, and familial atrial fibrillation. This gene exhibits tissue-specific imprinting, with preferential expression from the maternal allele in some tissues, and biallelic expression in others. This gene is located in a region of chromosome 11 amongst other imprinted genes that are associated with Beckwith-Wiedemann syndrome (BWS), and itself has been shown to be disrupted by chromosomal rearrangements in patients with BWS. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq,
KCNQ1 KCNA8 KCNA9 KVLQT1, Potassium voltage-gated channel subfamily KQT member 1 (IKs producing slow voltage-gated potassium channel subunit alpha KvLQT1) (KQT-like 1) (Voltage-gated potassium channel subunit Kv7.1)
1 mg/ml
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