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.
Description:
Mouse Anti-Human KCNQ4 Monoclonal Antibody
Host Species:
Mouse
Species Reactivity:
Human
Clone#:
S43-7
Isotype:
IgG1
Application:
ICC, IP, WB
Usage:
For Lab Research Use Only
Storage:
Store antibody products at 2-8°C. For long term storage, aliquot and freeze at -20°C. Avoid repeated freeze/thaw cycles