KCNQ4 Antibody - Cat. #: CSB-PA320879

SKU: CSB-PA320879

Size :50ul

Clone Number:

Aliases:DFNA 2 antibody; DFNA2 antibody; KCNQ 4 antibody; Kcnq4 antibody; KCNQ4_HUMAN antibody; KQT like 4 antibody; KQT-like 4 antibody; KV7.4 antibody; Potassium channel KQT like 4 antibody; Potassium channel subunit alpha KvLQT4 antibody; Potassium voltage gated channel KQT like protein 4 antibody; Potassium voltage gated channel KQT like subfamily member 4 antibody; Potassium voltage gated channel subfamily KQT member 4 antibody; Potassium voltage-gated channel subfamily KQT member 4 antibody; Voltage gated potassium channel subunit Kv7.4 antibody; Voltage-gated potassium channel subunit Kv7.4 antibody

Product Type:Polyclonal Antibody

Immunogen Species:Homo sapiens (Human)

UniProt ID:P56696

Immunogen:Synthetic peptide of Human KCNQ4

Raised in:Rabbit

Species Reactivity:Human, Mouse

Tested Applications:ELISA, WB, IHC; ELISA:1:1000-1:2000, WB:1:200-1:1000, IHC:1:50-1:200

Background:The protein encoded by this gene forms a potassium channel that is thought to play a critical role in the regulation of neuronal excitability, particularly in sensory cells of the cochlea. The current generated by this channel is inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. The encoded protein can form a homomultimeric potassium channel or possibly a heteromultimeric channel in association with the protein encoded by the KCNQ3 gene. Defects in this gene are a cause of nonsyndromic sensorineural deafness type 2 (DFNA2), an autosomal dominant form of progressive hearing loss. Two transcript variants encoding different isoforms have been found for this gene.

Clonality:Polyclonal

Isotype:IgG

Purification Method:Antigen affinity purification

Conjugate:Non-conjugated

Buffer:-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol

Form:Liquid

Stroage:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.

Target Names:KCNQ4

Research Areas:Neuroscience