Annexin II Polyclonal Antibody, 100ul[BT-AP00460] Centrifuge Tube (Bottle) Mutations in this gene cause

Mutations in this gene cause cranioectodermal dysplasia-1

but only one of them is protein-coding

Can interact with G/C-rich motifs from serotonin receptor promoter

are Ca(2+)/calmodulin (see CALM1

Members of this family can interact with the elongin B-C adapter complex via their SOCS box domain and further complex with the cullin and ring box proteins to form E3 ubiquitin ligase complexes

Annexin II Polyclonal Antibody, 100ul[BT-AP00460] Centrifuge Tube (Bottle) Mutations in this gene causeANXA2 encodes a member of the annexin family. Members of this calcium dependent phospholipid binding protein family play a role in the regulation of cellular growth and in signal transduction pathways. This protein functions as an autocrine factor which heightens osteoclast formation and bone resorption. ANXA2 has three pseudogenes located on chromosomes 4, 9 and 10, respectively. Multiple alternatively spliced transcript variants encoding different