SKAP1 Polyclonal Antibody, 20ul CellSafe™ Mutations in this gene cause

Mutations in this gene cause corneal fleck dystrophy (CFD)

Acts as a negative regulator of the Toll-like and IL-1R receptor signaling pathways

Mutations in this gene are associated with metaphyseal anadysplasia

High level of expression in lymphoid tissues

These family members are transcription factors that are implicated in a variety of cellular processes

SKAP1 Polyclonal Antibody, 20ul CellSafe™ Mutations in this gene causeThis gene encodes a T cell adaptor protein, a class of intracellular molecules with modular domains capable of recruiting additional proteins but that exhibit no intrinsic enzymatic activity. The encoded protein contains a unique N terminal region followed by a PH domain and C terminal SH3 domain. Along with the adhesion and degranulation promoting adaptor protein, the encoded protein plays a critical role in inside out signaling by coupling T cell