E2F-3 (Acetyl-Lys168) Polyclonal Antibody, 100ul Fluorescent Staining Defects in PRF1 cause familial

Defects in PRF1 cause familial hemophagocytic lymphohistiocytosis type 2 (HPLH2)

Multiple mutations in this gene have been identified

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

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

some of which are associated with Creutzfeldt-Jakob disease

E2F-3 (Acetyl-Lys168) Polyclonal Antibody, 100ul Fluorescent Staining Defects in PRF1 cause familialE2F3 (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