KCNH2 / Unconjugated /
Product Details
| Description | KCNH2 encodes a human homologue of the Drosophila melanogaster eag gene, a potassium channel protein. Along with five other human genes, mutations in KCNH2 that result in loss of function or dominant negative function cause long QT syndrome. | |
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| Conjugate | Unconjugated | |
| Clone | ||
| Target Species | Guinea Pig | |
| Applications | IHC-P | |
| Supplier | Aviva Systems Biology | |
| Catalog # | Sign in to view product details, citations, and spectra | |
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About KCNH2
This gene encodes a component of a voltage-activated potassium channel found in cardiac muscle, nerve cells, and microglia. Four copies of this protein interact with one copy of the KCNE2 protein to form a functional potassium channel. Mutations in this gene can cause long QT syndrome type 2 (LQT2). Transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, May 2022]
This gene encodes a component of a voltage-activated potassium channel found in cardiac muscle, nerve cells, and microglia. Four copies of this protein interact with one copy of the KCNE2 protein to form a functional potassium channel. Mutations in this gene can cause long QT syndrome type 2 (LQT2). Transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, May 2022]
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