CD20 Polyclonal Antibody, 50ul[BT-AP01398] Vortex Mixer Defects in this gene are

Defects in this gene are the cause of Werner syndrome| an autosomal recessive disorder characterized by premature aging

also known as phosphorylase kinase deficiency of liver and muscle

similarity:Belongs to the protein kinase superfamily

Elongator complex protein 2 encoded by ELP2 is a core subunit of the elongator complex

CD20 Polyclonal Antibody, 50ul[BT-AP01398] Vortex Mixer Defects in this gene areMS4A1 encodes a member of the membrane spanning 4A gene family. Members of this nascent protein family are characterized by common structural features and similar intron exon splice boundaries and display unique expression patterns among hematopoietic cells and nonlymphoid tissues. MS4A1 encodes a B lymphocyte surface molecule which plays a role in the development and differentiation of B cells into plasma cells. This family member is localized to