SNX3 Polyclonal Antibody, 20ul Pipette Micro Tips TNFSF12-TNFSF13

TNFSF12-TNFSF13

and gamma subunits that assemble through a coiled-coil domain

Mutations in this gene have been reported to be associated with nonsyndromic hearing loss

MED21 (mediator complex subunit 21) encodes a member of the mediator complex subunit 21 family

characterized by the lack of the A subunit alone

SNX3 Polyclonal Antibody, 20ul Pipette Micro Tips TNFSF12-TNFSF13SNX3 (sorting nexin 3) encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region, like most family members. This protein interacts with phosphatidylinositol 3 phosphate, and is involved in protein trafficking. A pseudogene of SNX3 is present on the sex chromosomes.