FGFR-4 Monoclonal Antibody, 100ul[BT-MCA0535] Cell Function Analysis Mutations in this gene are

Mutations in this gene are associated with infantile-onset multisystem autoimmune disease and hyper-immunoglobulin E syndrome

PRKDC (protein kinase

Translocations resulting in fusion proteins with both CRTC1 and CRTC3 have been implicated in the development of mucoepidermoid carcinomas

Introducing Cell Culture Dishes

Mutations in this gene are associated with microvillous inclusion disease

FGFR-4 Monoclonal Antibody, 100ul[BT-MCA0535] Cell Function Analysis Mutations in this gene areThe protein encoded by this gene is a member of the fibroblast growth factor receptor family, where amino acid sequence is highly conserved between members and throughout evolution. FGFR family members differ from one another in their ligand affinities and tissue distribution. A full length representative protein would consist of an extracellular region, composed of three immunoglobulin like domains, a single hydrophobic membrane spanning segment and