E2F-3 (Acetyl-Lys168) Polyclonal Antibody, 100ul Fluorescent Staining Mutations in this gene cause

Mutations in this gene cause arginine:glycine amidinotransferase deficiency| an inborn error of creatine synthesis characterized by mental retardation| language impairment| and behavioral disorders

The encoded protein binds directly to retinoblastoma protein

PPARA (peroxisome proliferator activated receptor alpha) encodes the subtype PPAR-alpha

Other members of this small family of engulfment and cell motility (ELMO) proteins have been shown to interact with the dedicator of cyto-kinesis 1 protein to promote phagocytosis and effect cell shape changes

Multiple mutations in this gene have been identified

E2F-3 (Acetyl-Lys168) Polyclonal Antibody, 100ul Fluorescent Staining Mutations in this gene causeE2F3 (E2F transcription factor 3) encodes a member of a small family of transcription factors that function through binding of DP interaction partner proteins. The encoded protein recognizes a specific sequence motif in DNA and interacts directly with the retinoblastoma protein (pRB) to regulate the expression of genes involved in the cell cycle. Altered copy number and activity of this gene have been observed in a number of human cancers. There are