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钾离子通道蛋白家族KCNQ1抗体
本产品不向个人销售，仅用作科学研究，不用于任何人体实验及非科研性质的动物实验。

产品名称
Anti-KCNQ1
Anti-potassium voltage-gated channel subfamily Q member 1 Antibody
产品介绍
靶标：

KCNQ1


产品别名：

ATFB1； ATFB3； JLNS1； KCNA8； KCNA9； KVLQT1； Kv1.9； Kv7.1； LQT； LQT1； RWS； SQT2； WRS； KCNQ1； potassium voltage-gated channel subfamily Q member 1； potassium voltage-gated channel subfamily Q member 1； potassium voltage-gated channel subfamily KQT member 1； IKs producing slow voltage-gated potassium channel subunit alpha KvLQT1； kidney and cardiac voltage dependend K+ channel； potassium channel, voltage gated KQT-like subfamily Q, member 1； potassium voltage-gated channel, KQT-like subfamily, member 1； slow delayed rectifier channel subunit； voltage-gated potassium channel subunit Kv7.1； 钾离子通道蛋白家族KCNQ1；


背景信息：
This gene encodes a voltage-gated potassium channel required for repolarization phase of the cardiac action potential. This protein can form heteromultimers with two other potassium channel proteins, KCNE1 and KCNE3. Mutations in this gene are associated with hereditary long QT syndrome 1 (also known as Romano-Ward syndrome), Jervell and Lange-Nielsen syndrome, and familial atrial fibrillation. This gene exhibits tissue-specific imprinting, with preferential expression from the maternal allele in some tissues, and biallelic expression in others. This gene is located in a region of chromosome 11 amongst other imprinted genes that are associated with Beckwith-Wiedemann syndrome (BWS), and itself has been shown to be disrupted by chromosomal rearrangements in patients with BWS. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq,

宿主：Rbt
类型：Pab
同种型:IgG  
应用：WB
纯化方式：亲和纯化
偶联物：Unconjugated
性状：液体
存储溶液：参阅说明书
浓度：Batch dependent (Please refer to the vial label for the specific concentration.)
稀释比例: Optimal dilutions/concentrations should be determined by the end user           
储存：经常使用则4°C保存。-20°C保存不超过两年。避免反复冻融。
注意事项：仅供实验室使用。不适用于人类或动物的任何临床，治疗或诊断用途。不适合动物或人类食用。