RIP2 Polyclonal Antibody, 100ul Diagnostic Probes & Oligos A genetic variation in IFNGR1

A genetic variation in IFNGR1 is associated with susceptibility to Helicobacter pylori infection

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These kelch-like repeats promote substrate ubiquitination of bound proteins via interaction of the BTB domain with the CUL3 (cullin 3) component of a cullin-RING E3 ubiquitin ligase (CRL) complex

Isoforms include a full-length transmembrane receptor isoform and shortened

The aberrant regulation of CTTN contributes to tumor cell invasion and metastasis

RIP2 Polyclonal Antibody, 100ul Diagnostic Probes & Oligos A genetic variation in IFNGR1RIPK2 (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.