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Human KCNQ4 Stable Cell Line-CHO

See other products for KCNQ4
Cat.No.
CSC-RI0148
Background
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.
Growth Properties
Adherent
Morphology
Epithelial-like
Host Cell
CHO-K1
Ship
Dry ice
Gene Information
Official Symbol
KCNQ4
Synonyms
KCNQ4; potassium voltage-gated channel, KQT-like subfamily, member 4; DFNA2; potassium voltage-gated channel subfamily KQT member 4; Kv7.4; potassium channel KQT-like 4; potassium channel subunit alpha KvLQT4; KV7.4; DFNA2A;
Gene ID
MIM
UniProt ID
P56696
Chromosome Location
1p34
Pathway
Cholinergic synapse, organism-specific biosystem; Neuronal System, organism-specific biosystem; Potassium Channels, organism-specific biosystem; Voltage gated Potassium channels, organism-specific biosystem;
Function
potassium channel activity; voltage-gated ion channel activity; voltage-gated potassium channel activity;
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Cat#
Product Name
Titer
Product Size
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Price
AD08459Z
>1x 10^9 vp/ml
1 x 0.2 ml
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Cat#
Product Name
Size/Form
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Price
MiUTR1M-06270
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MiUTR4H-TG04726
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Fax: 1-631-614-7828
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Email: info@creative-biogene.com
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45-1 Ramsey Road, Shirley, NY 11967, USA
Tel: 1-631-626-9181
Fax: 1-631-614-7828
Email: info@creative-biogene.com

Europe
Tel: 44-207-097-1828

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