KCNE1 Polyclonal Antibody, 100ul Vacuum Filter Mutations in this gene are

Mutations in this gene are the cause of autosomal recessive cortical juvenile-onset cataract

Both of these embryonic hemoglobins are normally supplanted by fetal

catalyze the hydrolysis of glycerophospholipids at the sn-2 position and then liberate free fatty acids and lysophospholipids (Chiba et al

Cadherin-2 plays a role in the establishment of left-right asymmetry

Two alternative transcript variants encoding different protein isoforms have been described for SNAP25

KCNE1 Polyclonal Antibody, 100ul Vacuum Filter Mutations in this gene areThe product of this gene belongs to the potassium channel KCNE family. Potassium ion channels are essential to many cellular functions and show a high degree of diversity, varying in their electrophysiologic and pharmacologic properties. This gene encodes a transmembrane protein known to associate with the product of the KVLQT1 gene to form the delayed rectifier potassium channel. Mutation in this gene are associated with both Jervell and Lange