KCNE1 Polyclonal Antibody, 100ul Vacuum Filter At least two transcript variants

At least two transcript variants encoding the same protein have been found for ATXN1 (ataxin 1)

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

Both of these embryonic hemoglobins are normally supplanted by fetal

Studies suggest that hexanucleotide expansions could result in the selective stabilization of repeat-containing pre-mRNA

KCNE1 Polyclonal Antibody, 100ul Vacuum Filter At least two transcript variantsThe 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