FA8A Rabbit Polyclonal Antibody, 50ul[BT-AP02610] Proteases MAPT gene mutations have been

MAPT gene mutations have been associated with several neurodegenerative disorders such as Alzheimer's disease| Pick's disease| frontotemporal dementia| cortico-basal degeneration and progressive supranuclear palsy

the encoded protein is a functional receptor for the spike glycoprotein of the human coronaviruses SARS and HCoV-NL63

CALML5 (calmodulin like 5) encodes a novel calcium binding protein expressed in the epidermis and related to the calmodulin family of calcium binding proteins

The encoded type II transmembrane protein is a downstream target of CCAAT/enhancer binding protein (C/EBP)| beta (CEBPB) and may play a role in inflammation

One pseudogene is known to exist

FA8A Rabbit Polyclonal Antibody, 50ul[BT-AP02610] Proteases MAPT gene mutations have beendisease: Defects in F8 are the cause of hemophilia A (HEMA)