Phospho-Caspase-9 (Y153) Polyclonal Antibody, 100ul Microplate Mixer Mutations in this gene are

Mutations in this gene are a cause of branchiootorenal syndrome type 2

Alternatively spliced transcript variants encoding different isoforms of this gene have been described

members of which deacetylate lysine residues on the N-terminal part of the core histones

is widely expressed whereas the RBMY gene evolved a male-specific function in spermatogenesis

Phospho-Caspase-9 (Y153) Polyclonal Antibody, 100ul Microplate Mixer Mutations in this gene areCASP9 (caspase 9) encodes a member of the cysteine aspartic acid protease (caspase) family. Sequential activation of caspases plays a central role in the execution phase of cell apoptosis. Caspases exist as inactive proenzymes which undergo proteolytic processing at conserved aspartic residues to produce two subunits, large and small, that dimerize to form the active enzyme. This protein can undergo autoproteolytic processing and activation by the