CABT-B9461

antibody from Creative Diagnostics
Targeting: KCNQ1 JLNS1, KCNA8, KCNA9, Kv7.1, KVLQT1, LQT, LQT1
Provider product page for CABT-B9461
Western blot
Flow cytometry

Antibody data

Product number
CABT-B9461 - Provider product page
Provider
Creative Diagnostics
Product name
Mouse anti-Human KCNQ1 monoclonal antibody, clone 6F23
Antibody type
Monoclonal
Description
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, Aug 2011]
Reactivity
Human
Host
Mouse
Conjugate
Unconjugated
Isotype
IgG
Antibody clone number
6F23
Vial size
100 _L
Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
KCNQ1 protein structure - CABT-B9461 shown in red.