KCNE1 Polyclonal Antibody, 100ul Vacuum Filter Two alternative transcript variants encoding

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

Mutations in this gene are a cause of hypomyelinating leukodystrophy

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

Both of these embryonic hemoglobins are normally supplanted by fetal

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

KCNE1 Polyclonal Antibody, 100ul Vacuum Filter Two alternative transcript variants encodingThe 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