JAK2(Phospho Tyr119) Polyclonal Antibody, 100ul Vessels Mutations in NECTIN4 are the

Mutations in NECTIN4 are the cause of ectodermal dysplasia-syndactyly syndrome type 1

Belongs to the transient receptor family

when GDP is bound

This gene encodes a member of the G protein-coupled receptor superfamily

This nuclear protein interacts with phosphorylated histone H2AX near sites of DNA double-strand breaks through its BRCT motifs

JAK2(Phospho Tyr119) Polyclonal Antibody, 100ul Vessels Mutations in NECTIN4 are theThis gene product is a protein tyrosine kinase involved in a specific subset of cytokine receptor signaling pathways. It has been found to be constituitively associated with the prolactin receptor and is required for responses to gamma interferon. Mice that do not express an active protein for this gene exhibit embryonic lethality associated with the absence of definitive erythropoiesis.