FBX22 Rabbit Polyclonal Antibody, 50ul Hybridoma Antibody Sequencing A mutation in this gene

A mutation in this gene was found in an individual with Leigh syndrome

transferring phosphorus-containing groups and protein kinase activity

Two transcript variants encoding different isoforms have been found for PRKCG

The protein encoded by this gene is a glycoprotein containing several von Willebrand factor C domains and epidermal growth factor (EGF)-like domains

FBX22 Rabbit Polyclonal Antibody, 50ul Hybridoma Antibody Sequencing A mutation in this geneThis gene encodes a member of the F box protein family which is characterized by an approximately 40 amino acid motif the F box. The F box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1 cullin F box) which function in phosphorylation dependent ubiquitination. The F box proteins are divided into 3 classes: Fbws containing WD 40 domains Fbls containing leucine rich repeats and Fbxs containing