TAAR8 Polyclonal Antibody, 50ul DNA Synthesis Mutations in this gene are

Mutations in this gene are the most common cause of Fanconi anemia

This protein was shown to activate antiapoptotic kinase AKT/PKB through a signaling complex involving SRC kinase and tumor necrosis factor receptor-associated factor (TRAF) 6

Additional transcript variants have been described but their full-length natures have not been experimentally verified

DDX55 encodes a member of protein family containing a characteristic Asp-Glu-Ala-Asp (DEAD) motif

Members of this family have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes

TAAR8 Polyclonal Antibody, 50ul DNA Synthesis Mutations in this gene areThis gene is part of the trace amine receptor cluster on chromosome 6 and encodes an orphan G protein coupled receptor. Upregulated expression of this gene in astroglial cells upon exposure to lipopolysaccharides suggests a function for the encoded protein in the brain.