| 产品详情 |
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| Antigenic Specificity | KCNQ1 |
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| Clone | polyclonal |
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| Host Species | Rabbit |
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| Reactive Species | human |
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| Isotype | n/a |
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| Format | peptide affinity purified |
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| Size | 80 µl, 400 µl |
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| Concentration | n/a |
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| Applications | WB. RUO |
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| Reviews / Ratings | If you have used this antibody, please help fellow researchers by submitting reviews to pAbmAbs and antYbuddY. |
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| Description | 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. This KCNQ1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 4-33 amino acids from the N-terminal region of human KCNQ1. |
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| Immunogen | Human KCNQ1. |
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| Other Names | KCNQ1; ATFB1; ATFB3; JLNS1; KCNA8; KCNA9; KVLQT1; Kv1.9; Kv7.1; LQT; LQT1; RWS; SQT2; WRS; KQT-like 1; ROMANO-WARD SYNDROME; Potassium voltage-gated channel subfamily KQT member 1; IKs producing slow voltage-gated potassium channel subunit alpha KvLQT1; Voltage-gated potassium channel subunit Kv7.1; potassium voltage-gated channel, KQT-like subfamily, member 1; FLJ26167; Jervell and Lange-Nielsen syndrome 1; kidney and cardiac voltage dependend K+ channel; long (elect |
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| Gene, Accession # | SwissProt: P51787 |
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| Catalog # | abx026614 |
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| Price | |
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| Order / More Info | KCNQ1 Antibody from ABBEXA |
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| Product Specific References | n/a |
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