ANR23 Rabbit Polyclonal Antibody, 100ul Vacuum Filter Mutations in SLC22A5 (solute carrier

Mutations in SLC22A5 (solute carrier family 22 member 5)are the cause of systemic primary carnitine deficiency (CDSP)

This protein is expressed in the canalicular (apical) part of the hepatocyte and functions in biliary transport

a protein that initiates a signaling cascade that leads to apoptosis when cells are subjected to cytotoxic stresses

See ZFP93 (MIM 604749) for additional information on zinc finger proteins

ANR23 Rabbit Polyclonal Antibody, 100ul Vacuum Filter Mutations in SLC22A5 (solute carrierThis gene is a member of the muscle ankyrin repeat protein (MARP) family and encodes a protein with four tandem ankyrin like repeats. The protein is localized to the nucleus, functioning as a transcriptional regulator. Expression of this protein is induced during recovery following starvation.