KCNH2 encodes a voltage-activated potassium channel belonging to the eag family. It shares sequence similarity with the Drosophila ether-a-go-go (eag) gene. Mutations in KCNH2 can cause long QT syndrome type 2 (LQT2). Transcript variants encoding distinct isoforms have been identified.
Human Potassium voltage-gated channel subfamily H member 2 (KCNH2) ELISA Kit employs a two-site sandwich ELISA to quantitate KCNH2 in samples. An antibody specific for KCNH2 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyKCNH2 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for KCNH2 is added to the wells. After washing, Streptavidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of KCNH2 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Human Potassium voltage-gated channel subfamily H member 2 (KCNH2) ELISA Kit listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.
Find more details at http://www.abbkine.com/product/human-potassium-voltage-gated-channel-subfamily-h-member-2-kcnh2-elisa-kit-kte61928/
bio-equip.cn
中文
