TIP60 Polyclonal Antibody, 50ul[BT-AP09044] Cellular Function Assays disease:Defects in MT-ND2 are a

disease:Defects in MT-ND2 are a cause of Leber hereditary optic neuropathy (LHON)

This gene encodes a member of the small ubiquitin-related modifier (SUMO) family of eukaryotic proteins

This gene encodes a member of the ARHGAP family of Rho/Rac/Cdc42-like GTPase activating proteins

The AZI1 gene is conserved in dog

TIP60 Polyclonal Antibody, 50ul[BT-AP09044] Cellular Function Assays disease:Defects in MT-ND2 are aThe lysine acetyltransferase 5 encoded by KAT5 belongs to the MYST family of histone acetyl transferases (HATs) and was originally isolated as an HIV 1 TAT interactive protein. HATs play important roles in regulating chromatin remodeling, transcription and other nuclear processes by acetylating histone and nonhistone proteins. This protein is a histone acetylase that has a role in DNA repair and apoptosis and is thought to play an important role in