KLHL13 Monoclonal Antibody, 100ul Aspirating Pipets and 3 cytoplasmic domains

and 3 cytoplasmic domains

The gene is deleted in Williams-Beuren syndrome| a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11

This gene is a member of the bestrophin gene family of anion channels

This protein functions as a monomer

KLHL13 Monoclonal Antibody, 100ul Aspirating Pipets and 3 cytoplasmic domainsThis gene encodes a BTB and kelch domain containing protein and belongs to the kelch repeat domain containing superfamily of proteins. The encoded protein functions as an adaptor protein that complexes with Cullin 3 and other proteins to form the Cullin 3 based E3 ubiquitin protein ligase complex. This complex is necessary for proper chromosome segregation and completion of cytokinesis. Alternate splicing results in multiple transcript variants.