CCDC8 Polyclonal Antibody, 20ul Vacuum Aspirator Microdeletions in this gene are

Microdeletions in this gene are associated with contiguous ABCD1/DXS1375E deletion syndrome (CADDS)

which is deleted in DiGeorge syndrome

It catalyzes its autophosphorylation on serine/threonine and tyrosine residues

This gene is a member of the GLI-similar zinc finger protein family and encodes a nuclear protein with five C2H2-type zinc finger domains

Inner/outer surfaces of the tube are smooth with an even luster

CCDC8 Polyclonal Antibody, 20ul Vacuum Aspirator Microdeletions in this gene areThis gene encodes a coiled coil domain containing protein. The encoded protein functions as a cofactor required for p53 mediated apoptosis following DNA damage, and may also play a role in growth through interactions with the cytoskeletal adaptor protein obscurin like 1. Mutations in this gene are a cause of 3M syndrome 3 (3M3).