Potassium Voltage-Gated Channel Subfamily KQT Member 3 (KCNQ3) Antibody

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Catalogue No: abx028226
Price: US$326.25
(Size: 80 µl)

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Datasheet SDS
The M channel is a slowly activating and deactivating potassium channel that plays a critical role in the regulation of neuronal excitability. The M channel is formed by the association of the protein encoded by this gene and one of two related proteins encoded by the KCNQ2 and KCNQ5 genes, both integral membrane proteins. M channel currents are inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. Defects in this gene are a cause of benign familial neonatal convulsions type 2 (BFNC2), also known as epilepsy, benign neonatal type 2 (EBN2).

Target Potassium Voltage-Gated Channel Subfamily KQT Member 3 (KCNQ3)
Clonality Polyclonal
Reactivity Mouse
Tested Applications ELISA, WB
Host Rabbit
Recommended dilutions WB: 1/1000. Optimal dilutions/concentrations should be determined by the end user.
Conjugation Unconjugated
Immunogen KLH-conjugated synthetic peptide between 651-679 amino acids from the C-terminal region of human KCNQ3.
Isotype IgG
Form Liquid
Purification Purified through a protein A column, followed by peptide affinity purification.
Storage Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
UniProt Primary AC O43525 (UniProt, ExPASy)
UniProt Secondary AC A2VCT8, B4DJY4, E7EQ89
UniProt Entry Name KCNQ3_HUMAN
Gene Symbol KCNQ3
KEGG hsa:3786
String 9606.ENSP00000373648
Molecular Weight Calculated MW: 96.7 kDa
Buffer PBS containing 0.09% sodium azide.
Availability Shipped within 5-10 working days.
Note This product is for research use only.
Research Articles on Potassium Voltage-Gated Channel Subfamily KQT Member 3 (KCNQ3)


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