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Human KCNQ4 Stable Cell Line-CHO
The human KCNQ4 gene encodes the pore-forming subunit of Kv7.4, a voltage-gated potassium channel. KCNQ4 loss-of-function mutations cause hereditary deafness. Kv7.4 channels expressed in neurons are therapeutic targets in seizure.
| Product Information | |
|---|---|
| Catalog #: | ACC-RI0148 |
| Gene Name: | KCNQ4 |
| Abbr | CHO-HuKCNQ4 |
| Alias | KCNQ4,DFNA2,Kv7.4,KV7.4,DFNA2A |
| Channel Subgroup | Voltage-gated (Kv) |
| Channel Type | Potassium Channel |
| Growth Properties | Adherent |
| Host Cell | CHO-K1 |
| Morphology | Epithelial-like |
| Product Format | frozen |
| Product Type | Ion Channel Expressing Cell |
| searchKeyword | KCNQ4,DFNA2,Kv7.4,KV7.4,DFNA2A |
| Shipping | Dry ice |
| Species | Human |
Related Products
| Catalog | Product Name | Gene Name | Species | Morphology | Price |
|---|---|---|---|---|---|
| ACC-RI0045 | Human KCNQ4 Stable Cell Line-HEK293 | KCNQ4 | Human | Epithelial | INQUIRY |
| ACC-RI0146 | Human KCNQ2/KCNQ4 Stable Cell Line-CHO | KCNQ4 | Human | Epithelial-like | INQUIRY |
Our products are only for research use. Not intended for any clinical or diagnostic use.
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