KCNQ1 Polyclonal Antibody, 100ul sgRNA Library Construction Mutations in this gene have

Mutations in this gene have been associated with limb-girdle muscular dystrophy

As membrane proteins on their way to degradation in lysosomes as part of their normal turn-over are also contained in the endosomal/lysosomal compartments

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KCNQ1 Polyclonal Antibody, 100ul sgRNA Library Construction Mutations in this gene haveThis 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