RIP2 Polyclonal Antibody, 50ul Protein Analysis This gene encodes a 39S

This gene encodes a 39S subunit protein which is more than twice the size of its E

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Mutations in this gene have been associated with Kenny-Caffey syndrome (KCS) type 2 and the more severe osteocraniostenosis (OCS| also known as Gracile Bone Dysplasia)| both characterized by short stature| hypoparathyroidism| bone development abnormalities| and hypocalcemia

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Additional transcript variants have been described in publications but their full-length sequence has not been determined

RIP2 Polyclonal Antibody, 50ul Protein Analysis This gene encodes a 39SRIPK2 (receptor interacting serine threonine kinase 2) encodes a member of the receptor interacting protein (RIP) family of serine threonine protein kinases. The encoded protein contains a C terminal caspase activation and recruitment domain (CARD), and is a component of signaling complexes in both the innate and adaptive immune pathways. It is a potent activator of NF kappaB and inducer of apoptosis in response to various stimuli.