IFN-Gamma Monoclonal Antibody, 100ul[BT-MCA0098] Tubes a multisystem developmental disorder caused

a multisystem developmental disorder caused by deletion of multiple genes at 7q11

FGR is a member of the Src family of protein tyrosine kinases (PTKs)

Component of a multimeric complex involved in the transduction of antiproliferative and homotypic adhesion signals

DED is a protein-protein interaction domain shared by adaptors

A similar murine protein interacts with TNFR-associated factor 1 (TRAF1)| TNFR-associated factor 2 (TRAF2)| and cylindromatosis

IFN-Gamma Monoclonal Antibody, 100ul[BT-MCA0098] Tubes a multisystem developmental disorder causedThis gene encodes a soluble cytokine that is a member of the type II interferon class. The encoded protein is secreted by cells of both the innate and adaptive immune systems. The active protein is a homodimer that binds to the interferon gamma receptor which triggers a cellular response to viral and microbial infections. Mutations in this gene are associated with an increased susceptibility to viral, bacterial and parasitic infections and to several