Home Antibody All anti-KCNQ1 antibodies
Anti-KCNQ1 Antibody S37A-10
Also for KCNQ1 (NM_000218)
|Fusion protein amino acids 2-101 of human KCNQ1, accession number P51787|
|Human, Mouse, Rat
||WB, IP, IHC
|PBS pH7.2, 50% glycerol|
|Homo sapiens potassium voltage-gated channel, KQT-like subfamily, member 1 (KCNQ1), transcript variant 1|
|ATFB1; ATFB3; JLNS1; KCNA8; KCNA9; Kv1.9; Kv7.1; KVLQT1; LQT; LQT1; RWS; SQT2; WRS|
|This gene encodes a voltage-gated potassium channel required for the repolarization phase of the cardiac action potential. The gene product can form heteromultimers with two other potassium channel proteins, KCNE1 and KCNE3. Mutations in this gene are associated with hereditary long QT syndrome (also known as Romano-Ward syndrome), Jervell and Lange-Nielsen syndrome and familial atrial fibrillation. The gene is located in a region of chromosome 11 that contains a number of contiguous genes, which are abnormally imprinted in cancer and the Beckwith-Wiedemann syndrome. This gene is also imprinted, with preferential expression from the maternal allele in some tissues, excluding cardiac muscle. Alternatively spliced transcripts encoding distinct isoforms have been described. [provided by RefSeq]. |
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Western blot analysis of KCNQ1 in T-Cho cells using a 1:1000 dilution of SMC-307.
Western blot analysis of KCNQ1 in a human cell line mix using a 1:1000 dilution of SMC-307.
IHC analysis of KCNQ1 in mouse brain tissue using SMC-307.